109 results on '"Shapiro O"'
Search Results
2. Vibrio coralliilyticus infection triggers a behavioural response and perturbs nutritional exchange and tissue integrity in a symbiotic coral
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Gibbin, E., Gavish, A., Krueger, T., Kramarsky-Winter, E., Shapiro, O., Guiet, R., Jensen, L., Vardi, A., and Meibom, A.
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- 2019
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3. Using NanoSIMS coupled with microfluidics to visualize the early stages of coral infection by Vibrio coralliilyticus
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Gibbin, E., Gavish, A., Domart-Coulon, I., Kramarsky-Winter, E., Shapiro, O., Meibom, A., and Vardi, A.
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- 2018
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4. Congenital Conditions
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Bratslavsky, G., primary, Shapiro, O., additional, and Riddell, J.V.B., additional
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- 2013
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5. Genetic Diseases
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Shapiro, O., primary and Bratslavsky, G., additional
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- 2013
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6. 787P Urachal (URAC) and non-urachal (NURAC) adenocarcinomas of the urinary bladder: A comparative comprehensive genomic profiling (CGP) study
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Bratslavsky, G., primary, Grivas, P., additional, Necchi, A., additional, Shapiro, O., additional, Jacob, J., additional, Elvin, J., additional, Vergilio, J-A., additional, Lin, D.I., additional, Williams, E., additional, Hiemenz, M., additional, Tse, J., additional, Lechpammer, M., additional, Killian, J.K., additional, Ramkissoon, S., additional, Severson, E., additional, Hemmerich, A., additional, Huang, R., additional, Duncan, D., additional, Danziger, N.A., additional, and Ross, J.S., additional
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- 2020
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7. Contrasting genomic profiles in post-systemic treatment metastatic sites (MET) and pre-treatment primary tumors (PT) of clinically advanced prostate cancer (PC)
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Necchi, A., primary, Grivas, P., additional, Bratslavsky, G., additional, Shapiro, O., additional, Jacob, J., additional, Sokol, E., additional, Vergilio, J., additional, Killian, J., additional, Lin, D., additional, Haberberger, J., additional, Tse, J., additional, Ramkissoon, S., additional, Severson, E., additional, Hemmerich, A., additional, Huang, R., additional, Ali, S., additional, Chung, J., additional, Madison, R., additional, Alexander, B., additional, Reddy, P., additional, Elvin, J., additional, Schrock, A., additional, Danziger, N., additional, and Ross, J., additional
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- 2020
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8. Malignant non-adrenal paraganglioma (mPara) and adrenal pheochromocytoma (mPheo) a comparative comprehensive genomic profiling (CGP) study
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Bratslavsky, G., primary, Sokol, E.S., additional, Necchi, A., additional, Shapiro, O., additional, Jacob, J., additional, Liu, N., additional, Elvin, J.A., additional, Vergilio, J.-A., additional, Killian, J.K., additional, Ngo, N., additional, Lin, D., additional, Ramkissoon, S., additional, Severson, E., additional, Ali, S.M., additional, Schrock, A.B., additional, Chung, J., additional, Reddy, P., additional, Alexander, B.M., additional, Miller, V.A., additional, and Ross, J.S., additional
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- 2019
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9. Vibrio coralliilyticus infection triggers a behavioural response and perturbs nutritional exchange and tissue integrity in a symbiotic coral
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Gibbin, E., primary, Gavish, A., additional, Krueger, T., additional, Kramarsky-Winter, E., additional, Shapiro, O., additional, Guiet, R., additional, Jensen, L., additional, Vardi, A., additional, and Meibom, A., additional
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- 2018
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10. Abstract No. 572 Renal access for repeat percutaneous nephrolithotomy in patients with recurrent kidney stones: feasibility, safety and endourologic procedure outcomes
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Chappell, M., primary, Kobayashi, K., additional, Durwas, K., additional, Zhang, D., additional, Shapiro, O., additional, and Karmel, M., additional
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- 2018
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11. Abstract No. 570 Nephroureteral access prior to percutaneous nephrolithotomy for staghorn calculi: comparative study with non-staghorn calculi on feasibility, safety, and surgical outcomes
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Kobayashi, K., primary, Skummer, P., additional, Chappell, M., additional, Zhang, D., additional, Shapiro, O., additional, and Karmel, M., additional
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- 2018
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12. 512O - Malignant non-adrenal paraganglioma (mPara) and adrenal pheochromocytoma (mPheo) a comparative comprehensive genomic profiling (CGP) study
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Bratslavsky, G., Sokol, E.S., Necchi, A., Shapiro, O., Jacob, J., Liu, N., Elvin, J.A., Vergilio, J.-A., Killian, J.K., Ngo, N., Lin, D., Ramkissoon, S., Severson, E., Ali, S.M., Schrock, A.B., Chung, J., Reddy, P., Alexander, B.M., Miller, V.A., and Ross, J.S.
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- 2019
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13. Urosepsis following percutaneous nephroureteral access prior to nephrolithotomy: incidence and risk factors
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Quinzi, D, primary, Kobayashi, K, additional, Samuel, M, additional, Skummer, P, additional, Zhang, D, additional, Jawed, M, additional, Shapiro, O, additional, and Karmel, M, additional
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- 2017
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14. Percutaneous nephrolithotomy for radiolucent stones: Feasibility and safety of nephroureteral access
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Kobayashi, K, primary, Quinzi, D, additional, Samuel, M, additional, Skummer, P, additional, Jawed, M, additional, Zhang, D, additional, Shapiro, O, additional, and Karmel, M, additional
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- 2017
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15. Vibrio coralliilyticusinfection triggers a behavioural response and perturbs nutritional exchange and tissue integrity in a symbiotic coral
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Gibbin, E., Gavish, A., Krueger, T., Kramarsky-Winter, E., Shapiro, O., Guiet, R., Jensen, L., Vardi, A., and Meibom, A.
- Abstract
Under homoeostatic conditions, the relationship between the coral Pocillopora damicornisand Vibrio coralliilyticusis commensal. An increase in temperature, or in the abundance of V. coralliilyticus, can turn this association pathogenic, causing tissue lysis, expulsion of the corals’ symbiotic algae (genus Symbiodinium), and eventually coral death. Using a combination of microfluidics, fluorescence microscopy, stable isotopes, electron microscopy and NanoSIMS isotopic imaging, we provide insights into the onset and progression of V. coralliilyticusinfection in the daytime and at night, at the tissue and (sub-)cellular level. The objective of our study was to connect the macro-scale behavioural response of the coral to the micro-scale nutritional interactions that occur between the host and its symbiont. In the daytime, polyps enhanced their mucus production, and actively spewed pathogens. Vibrioinfection primarily resulted in the formation of tissue lesions in the coenosarc. NanoSIMS analysis revealed infection reduced 13C-assimilation in Symbiodinium, but increased 13C-assimilation in the host. In the night incubations, no mucus spewing was observed, and a mucus film was formed on the coral surface. Vibrioinoculation and infection at night showed reduced 13C-turnover in Symbiodinium, but did not impact host 13C-turnover. Our results show that both the nutritional interactions that occur between the two symbiotic partners and the behavioural response of the host organism play key roles in determining the progression and severity of host-pathogen interactions. More generally, our approach provides a new means of studying interactions (ranging from behavioural to metabolic scales) between partners involved in complex holobiont systems, under both homoeostatic and pathogenic conditions.
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- 2019
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16. Gas vesicles isolated from Halobacterium cells by lysis in hypotonic solution are structurally weakened
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Oren, A, Pri-El, N, Shapiro, O, and Siboni, N
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Halobacterium ,Protein Denaturation ,Bacteriolysis ,Bacterial Proteins ,Hypotonic Solutions ,Osmotic Pressure ,Cytoplasmic Vesicles ,Hydrostatic Pressure ,Proteins ,Membrane Proteins ,Microbiology - Abstract
Analysis of pressure-collapse curves of Halobacterium cells containing gas vesicles and of gas vesicles released from such cells by hypotonic lysis shows that the isolated gas vesicles are considerably weaker than those present within the cells: their mean critical collapse pressure was around 0.049-0.058 MPa, as compared to 0.082-0.095 MPa for intact cells. The hypotonic lysis procedure, which is widely used for the isolation of gas vesicles from members of the Halobacteriaceae, thus damages the mechanical properties of the vesicles. The phenomenon can possibly be attributed to the loss of one or more structural gas vesicle proteins such as GvpC, the protein that strengthens the vesicles built of GvpA subunits: Halobacterium GvpC is a highly acidic, typically "halophilic" protein, expected to denature in the absence of molar concentrations of salt. © 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
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- 2005
17. Ir and PMR spectra and structure of zirconium and hafnium borohydrides
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Volkov, V. V., Sobolev, E. V., Zaev, E. E., and Shapiro, O. I.
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- 1968
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18. Abstract No. 521 - Percutaneous nephrolithotomy for radiolucent stones: Feasibility and safety of nephroureteral access
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Kobayashi, K, Quinzi, D, Samuel, M, Skummer, P, Jawed, M, Zhang, D, Shapiro, O, and Karmel, M
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- 2017
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19. 3:09 PMAbstract No. 323 - Urosepsis following percutaneous nephroureteral access prior to nephrolithotomy: incidence and risk factors
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Quinzi, D, Kobayashi, K, Samuel, M, Skummer, P, Zhang, D, Jawed, M, Shapiro, O, and Karmel, M
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- 2017
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20. Buoyancy studies in natural communities of square gas-vacuolate archaea in saltern crystallizer ponds.
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Oren, A, Pri-El, N, Shapiro, O, Siboni, N, Oren, A, Pri-El, N, Shapiro, O, and Siboni, N
- Abstract
BACKGROUND: Possession of gas vesicles is generally considered to be advantageous to halophilic archaea: the vesicles are assumed to enable the cells to float, and thus reach high oxygen concentrations at the surface of the brine. RESULTS: We studied the possible ecological advantage of gas vesicles in a dense community of flat square extremely halophilic archaea in the saltern crystallizer ponds of Eilat, Israel. We found that in this environment, the cells' content of gas vesicles was insufficient to provide positive buoyancy. Instead, sinking/floating velocities were too low to permit vertical redistribution. CONCLUSION: The hypothesis that the gas vesicles enable the square archaea to float to the surface of the brines in which they live was not supported by experimental evidence. Presence of the vesicles, which are mainly located close to the cell periphery, may provide an advantage as they may aid the cells to position themselves parallel to the surface, thereby increasing the efficiency of light harvesting by the retinal pigments in the membrane.
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- 2006
21. Efficacy and Morbidity of Therapeutic Renal Embolization in the Spectrum of Urologic Disease
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Jacobson, Avi I., primary, Amukele, S.A., additional, Marcovich, R., additional, Shapiro, O., additional, Shetty, R., additional, Aldana, J. P., additional, Lee, Benjamin R., additional, Smith, Arthur D., additional, and Siegel, D.N., additional
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- 2003
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22. Resolution enhancement of X-ray CT by spatial and temporal MLEM deconvolution correction.
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Carmi, R., Shapiro, O., and Braunstein, D.
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- 2004
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23. Software Acquisition Process (SWAP) Model FY81
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Shapiro, O., primary
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- 1982
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24. Description of the Software Acquisition Process (SWAP) Model.
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Shapiro, O., primary
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- 1984
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25. THE ROLE OF REGIONAL ORGANIZATION IN RURAL DEVELOPMENT IN ISRAEL -- SOME PRELIMINARY REMARKS.
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Weintraub, D. and Shapiro, O.
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RURAL development ,ORGANIZATION ,SOCIAL systems ,SOCIOLOGY ,SYSTEMS theory - Abstract
Copyright of Sociologia Ruralis is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 1965
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26. Automatic Tracking Of Laser And Electron Beam Intersection.
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Turko, B.T., Fuzesy, R.Z., Pripstein, D.A., Kowitt, M., Chamberlain, O., Shapiro, O., and Hughes, E.
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- 1990
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27. Software Acquisition Process (SWAP) Model FY81
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MITRE CORP BEDFORD MA, Shapiro, O., MITRE CORP BEDFORD MA, and Shapiro, O.
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The SWAP (Software Acquisition Process) Model is a software cost and schedule estimating tool that operates by simulating the acquisition process. Currently, SWAP simulates only the acquisition of embedded software in Full Scale Development. It can support more diverse usage. This report describes the Model's concepts, developmental approach, current status, and future plans, as of the completion of the second full year of its development. (Author)
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- 1982
28. Description of the Software Acquisition Process (SWAP) Model.
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MITRE CORP BEDFORD MA, Shapiro,O, MITRE CORP BEDFORD MA, and Shapiro,O
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The software Acquisition Process (SWAP) Model is a software cost and schedule estimating tool that operates by simulating the acquisition process. Its current implementation is tailored to reflect the Air Force 800 series regulations that apply to the Full Scale Development phase of the system acquisition process. This document details the acquisition depicted by the Model, the concepts underlying its simulation, its current status, and instructions for operating the Model. (Author)
- Published
- 1984
29. An Improved Method for Separation of Radioactive Thyroid Hormone Metabolites by Thin-Layer Chromatography.∗.
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Shapiro, O. and Gordon, A.
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- 1966
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30. Metabolic fluxes and chemical signaling during coral disease at the single cell-level
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Gibbin, Emma Mary, Gavish, A., Kramarsky-Winter, E., Shapiro, O., Meibom, Anders, and Vardi, A.
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fungi ,technology, industry, and agriculture ,population characteristics ,biochemical phenomena, metabolism, and nutrition ,geographic locations - Abstract
Metabolic fluxes and chemical signaling during coral disease at the single cell-level.
31. An Improved Method for Separation of Radioactive Thyroid Hormone Metabolites by Thin-Layer Chromatography.
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Shapiro, O., primary and Gordon, A., additional
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- 1966
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32. Resolution enhancement of X-ray CT by spatial and temporal MLEM deconvolution correction
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Carmi, R., primary, Shapiro, O., additional, and Braunstein, D., additional
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33. Automatic Tracking Of Laser And Electron Beam Intersection
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Turko, B.T., primary, Fuzesy, R.Z., additional, Pripstein, D.A., additional, Kowitt, M., additional, Chamberlain, O., additional, Shapiro, O., additional, and Hughes, E., additional
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34. Using NanoSIMS coupled with microfluidics to visualize the early stages of coral infection by <italic>Vibrio coralliilyticus</italic>.
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Gibbin, E., Gavish, A., Domart-Coulon, I., Kramarsky-Winter, E., Shapiro, O., Meibom, A., and Vardi, A.
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VIBRIO ,CORAL diseases ,PATHOGENIC microorganisms ,TRANSMISSION electron microscopy ,IMMUNITY ,STABLE isotopes ,GLOBAL warming - Abstract
Background: Global warming has triggered an increase in the prevalence and severity of coral disease, yet little is known about coral/pathogen interactions in the early stages of infection. The point of entry of the pathogen and the route that they take once inside the polyp is currently unknown, as is the coral's capacity to respond to infection. To address these questions, we developed a novel method that combines stable isotope labelling and microfluidics with transmission electron microscopy (TEM) and nanoscale secondary ion mass spectrometry (NanoSIMS), to monitor the infection process between
Pocillopora damicornis andVibrio coralliilyticus under elevated temperature. Results: Three coral fragments were inoculated with15 N-labeledV. coralliilyticus and then fixed at 2.5, 6 and 22 hpost- inoculation (hpi) according to the virulence of the infection. Correlative TEM/NanoSIMS imaging was subsequently used to visualize the penetration and dispersal ofV. coralliilyticus and their degradation or secretion products. Most of theV. coralliilyticus cells we observed were located in the oral epidermis of the fragment that experienced the most virulent infection (2.5 hpi). In some cases, these bacteria were enclosed within electron dense host-derived intracellular vesicles.15 N-enriched pathogen-derived breakdown products were visible in all tissue layers of the coral polyp (oral epidermis, oral gastrodermis, aboral gastrodermis), at all time points, although the relative15 N-enrichment depended on the time at which the corals were fixed. Tissues in the mesentery filaments had the highest density of15 N-enriched hotspots, suggesting these tissues act as a "collection and digestion" site for pathogenic bacteria. Closer examination of the sub-cellular structures associated with these15 N-hotspots revealed these to be host phagosomal and secretory cells/vesicles. Conclusions: This study provides a novel method for tracking bacterial infection dynamics at the levels of the tissue and single cell and takes the first steps towards understanding the complexities of infection at the microscale, which is a crucial step towards understanding how corals will fare under global warming. [ABSTRACT FROM AUTHOR]- Published
- 2018
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35. Valproic acid decreases urothelial cancer cell proliferation and induces thrombospondin-1 expression
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Byler Timothy K, Leocadio Dean, Shapiro Oleg, Bratslavsky Gennady, Stodgell Christopher J, Wood Ronald W, Messing Edward M, and Reeder Jay E
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Bladder cancer ,Valproic acid ,Thrombospondin-1, Urothelial carcinoma ,Gene expression ,Diseases of the genitourinary system. Urology ,RC870-923 - Abstract
Abstract Background Prevention of bladder cancer recurrence is a central challenge in the management of this highly prevalent disease. The histone deacetylase inhibitor valproic acid (sodium valproate) has anti-angiogenic properties and has been shown to decrease bladder cancer growth in model systems. We have previously shown reduced expression of thrombospondin-1 in a mouse model and in human bladder cancer relative to normal urothelium. We speculated that inhibition of angiogenesis by valproate might be mediated by this anti-angiogenic protein. Methods Bladder cancer cell lines UMUC3 and T24 were treated with valproate or another histone deacetylase inhibitor, vorinostat, in culture for a period of three days. Proliferation was assessed by alamar blue reduction. Gene expression was evaluated by reverse transcription of RNA and quantitative PCR. Results Proliferation assays showed treatment with valproate or vorinostat decreased proliferation in both cell lines. Histone deacetylase inhibition also increased relative expression of thrombospondin-1 up to 8 fold at 5 mM valproate. Conclusions Histone deacetylase inhibitors warrant further study for the prevention or treatment of bladder cancer.
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- 2012
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36. Comprehensive Assessment of Immuno-oncology Biomarkers in Adenocarcinoma, Urothelial Carcinoma, and Squamous-cell Carcinoma of the Bladder
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Andrea Necchi, Daniele Raggi, Jonathan Keith Killian, Nhu Ngo, Jon Chung, Joseph M. Jacob, Julia A. Elvin, Eric Allan Severson, Petros Grivas, Gennady Bratslavsky, Shakti H. Ramkissoon, Russell Madison, Richard S.P. Huang, Brian M. Alexander, Vincent A. Miller, Jeffrey S. Ross, Amanda Hemmerich, Prasanth Reddy, Oleg Shapiro, Siraj M. Ali, Alexa B. Schrock, Jo-Anne Vergilio, Necchi, A., Madison, R., Raggi, D., Jacob, J. M., Bratslavsky, G., Shapiro, O., Elvin, J. A., Vergilio, J. -A., Killian, J. K., Ngo, N., Ramkissoon, S., Severson, E., Hemmerich, A. C., Huang, R., Ali, S. M., Chung, J. H., Reddy, P., Miller, V. A., Schrock, A. B., Gay, L. M., Alexander, B. M., Grivas, P., and Ross, J. S.
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Male ,Oncology ,medicine.medical_specialty ,Bladder Squamous Cell Carcinoma ,Urology ,medicine.medical_treatment ,030232 urology & nephrology ,Immunotherapy biomarkers ,Adenocarcinoma ,Deep sequencing ,Bladder adenocarcinoma ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Biomarkers, Tumor ,medicine ,Carcinoma ,Humans ,Bladder squamous-cell carcinoma ,Genomic alterations ,Aged ,Retrospective Studies ,Carcinoma, Transitional Cell ,Genome ,Bladder cancer ,business.industry ,Variant histologies ,Microsatellite instability ,Immunotherapy ,Genetic Profile ,Middle Aged ,medicine.disease ,Urinary Bladder Neoplasms ,030220 oncology & carcinogenesis ,Carcinoma, Squamous Cell ,Immunohistochemistry ,Female ,business - Abstract
In patients with rare histologies of bladder cancer, including adenocarcinoma of the bladder (ACB) and squamous-cell carcinoma (SCC), there are limited standard therapy options, defining an unmet medical need.In this comparative comprehensive genomic profiling (CGP) study, genomic alterations (GAs), and immuno-oncology (IO) biomarkers have been analyzed.Within the Foundation Medicine database, 143 cases with centrally reviewed pure ACB, 2142 with pure urothelial carcinoma (UC), and 83 with pure SCC were subjected to CGP. All patients developed advanced disease following a primary diagnosis of bladder cancer.CGP using a hybrid capture-based assay and immunohistochemistry (IHC).Tumor mutational burden (TMB) was determined on 1.1 Mbp of sequenced DNA, and microsatellite instability (MSI) was determined on 114 loci. Programmed cell-death ligand-1 (PD-L1) expression was determined by IHC (Ventana SP-142 assay), with1% tumor cells (TCs) or tumor-infiltrating lymphocytes (TILs) scoring positive.Pure ACB patients were younger and more often female than pure UC and pure SCC patients. UC and SCC had a significantly higher median TMB than ACB (p0.001). Rare CD274 (PD-L1) amplification cases were more frequently seen in SCC than in UC (5% vs 1%), and were not seen in ACB. MSI high status was very uncommon in all tumor types (0-1%). The frequencies of PD-L1 expression in both TCs and TILs was higher in UC and SCC (both 30%) than in ACB (18%). The results are limited by their retrospective nature and lack of clinical data annotation.Deep sequencing revealed significant differences in IO biomarkers among the three major subtypes of bladder carcinomas. UC and SCC revealed higher frequencies of PD-L1 expression and higher TMB than ACB, and SCC has the highest frequency of CD274 amplification. The presence of pure SCC features should not disqualify patients for inclusion in IO trials.Tumor samples from patients diagnosed with advanced pure adenocarcinoma of the bladder (ACB) or pure squamous-cell carcinoma (SCC) have been analyzed in terms of frequency of putative immunotherapy biomarkers. The results indicated that pure SCC of the bladder was characterized by genomic features that portend similar response possibilities to immunotherapy compared with the classical pure urothelial carcinoma. Conversely, for pure ACB there might be different therapeutic opportunities, such as targeted therapies against peculiar genomic alterations in selected patients.
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- 2020
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37. Clinically Advanced Pheochromocytomas and Paragangliomas: A Comprehensive Genomic Profiling Study
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Joseph M. Jacob, Natalie Danziger, Nick Liu, Karel Pacak, Mehdi Mollapour, Andrea Necchi, Gennady Bratslavsky, Richard S.P. Huang, Hanan Goldberg, Jeffrey S. Ross, Ruben Pinkhasov, Tom S Sanford, Ethan Sokol, Oleg Shapiro, Shakti H. Ramkissoon, Michael Daneshvar, Jonathan Keith Killian, Eric Allan Severson, Bratslavsky, G., Sokol, E. S., Daneshvar, M., Necchi, A., Shapiro, O., Jacob, J., Liu, N., Sanford, T. S., Pinkhasov, R., Goldberg, H., Killian, J. K., Ramkissoon, S., Severson, E. A., Huang, R. S. P., Danziger, N., Mollapour, M., Ross, J. S., and Pacak, K.
- Subjects
0301 basic medicine ,Cancer Research ,SDHA ,Germline ,Article ,Paraganglioma ,Pheochromocytoma ,03 medical and health sciences ,paraganglioma ,0302 clinical medicine ,Germline mutation ,medicine ,PTEN ,Comprehensive genomic profiling ,Gene ,RC254-282 ,biology ,business.industry ,comprehensive genomic profiling ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Microsatellite instability ,genomic alterations ,medicine.disease ,pheochromocytoma ,030104 developmental biology ,Oncology ,030220 oncology & carcinogenesis ,Genomic ,biology.protein ,Cancer research ,Alterations pheochromocytoma ,business - Abstract
Simple Summary Clinically advanced pheochromocytomas and paragangliomas are a rare form of endocrine malignancy which can occur in familial and sporadic clinical settings and feature a variety of genomic alterations. Comprehensive genomic profiling (CGP) was performed to characterize the genomic alterations (GA) in clinically advanced disease to enable the search for potential therapy targets. Although the GA/tumor is relatively low for clinically advanced disease, CGP can reveal important potential targets for therapy in the metastatic setting including RET, NF1 and FGFR1. Based on this data, further study of CGP as a method of developing precision therapies for clinically advanced disease appears warranted. Abstract Patients with clinically advanced paragangliomas (CA-Para) and pheochromocytomas (CA-Pheo) have limited surgical or systemic treatments. We used comprehensive genomic profiling (CGP) to compare genomic alterations (GA) in CA-Para and CA-Pheo to identify potential therapeutic targets. Eighty-three CA-Para and 45 CA-Pheo underwent hybrid-capture-based CGP using a targeted panel of 324 genes. Tumor mutational burden (TMB) and microsatellite instability (MSI) were determined. The GA/tumor frequencies were low for both tumor types (1.9 GA/tumor for CA-Para, 2.3 GA/tumor for CA-Pheo). The most frequent potentially targetable GA in CA-Para were in FGFR1 (7%, primarily amplifications), NF1, PTEN, NF2, and CDK4 (all 2%) and for CA-Pheo in RET (9%, primarily fusions), NF1 (11%) and FGFR1 (7%). Germline mutations in known cancer predisposition genes were predicted in 13 (30%) of CA-Pheo and 38 (45%) of CA-Para cases, predominantly involving SDHA/B genes. Both CA-Para and CA-Para had low median TMB, low PD-L1 expression levels and none had MSI high status. While similar GA frequency is seen in both CA-Para and CA-Para, germline GA were seen more frequently in CA-Para. Low PD-L1 expression levels and no MSI high status argue against strong potential for novel immune checkpoint inhibitors. However, several important potential therapeutic targets in both CA-Para and CA-Para are identified using CGP.
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- 2021
38. Basal cell carcinoma of the prostate: a case report.
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Stearns G, Cheng JS, Shapiro O, and Nsouli I
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- 2012
39. Comprehensive genomic profiling of histologic subtypes of urethral carcinomas
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Brian M. Alexander, Amanda Hemmerich, Daniel Duncan, Prasanth Reddy, Russell Madison, Richard S.P. Huang, Douglas I. Lin, Jeffrey S. Ross, Erik A. Williams, Clair Edgerly, Naomi L Ferguson, Oleg Shapiro, Jeffrey M. Venstrom, Michael Hughes, Alexa B. Schrock, Jonathan Keith Killian, Ahmad Talal, Shakti H. Ramkissoon, Julia A. Elvin, Thomas Sanford, Gennady Bratslavsky, Julie Y. Tse, Jo-Anne Vergilio, Mehdi Mollapour, Petros Grivas, Joseph M. Jacob, Dean Pavlick, Eric Allan Severson, Kimberly McGregor, Jon Chung, Ethan Sokol, Natalie Danziger, Andrea Necchi, Jacob, J., Necchi, A., Grivas, P., Hughes, M., Sanford, T., Mollapour, M., Shapiro, O., Talal, A., Sokol, E., Vergilio, J. -A., Killian, J., Lin, D., Williams, E., Tse, J., Ramkissoon, S., Severson, E., Hemmerich, A., Ferguson, N., Edgerly, C., Duncan, D., Huang, R., Chung, J., Madison, R., Alexander, B., Venstrom, J., Reddy, P., Mcgregor, K., Elvin, J., Schrock, A., Danziger, N., Pavlick, D., Ross, J., and Bratslavsky, G.
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Adult ,Male ,Oncology ,medicine.medical_specialty ,Urology ,030232 urology & nephrology ,Malignancy ,03 medical and health sciences ,Tumor Status ,0302 clinical medicine ,Internal medicine ,Carcinoma ,medicine ,Humans ,PTEN ,Targeted cancer therapy ,Cancer genetics ,Urethral cancer ,Aged ,Aged, 80 and over ,Urethral Neoplasms ,biology ,Genitourinary system ,business.industry ,Microsatellite instability ,Genomics ,Middle Aged ,medicine.disease ,030220 oncology & carcinogenesis ,biology.protein ,Female ,business ,Clear cell - Abstract
Background Carcinoma of the urethra (UrthCa) is an uncommon Genitourinary (GU) malignancy that can progress to advanced metastatic disease. Methods One hundred twenty-seven metastatic UrthCa underwent hybrid capture-based comprehensive genomic profiling to evaluate all classes of genomic alterations (GA). Tumor mutational burden was determined on up to 1.1 Mbp of sequenced DNA, and microsatellite instability was determined on 114 loci. PD-L1 expression was determined by IHC (Dako 22C3). Results Forty-nine (39%) urothelial (UrthUC), 31 (24%) squamous (UrthSCC), 24 (19%) adenocarcinomas NOS (UrthAC), and 12 (9%) clear cell (UrthCC) were evaluated. UrthUC and UrthSCC are more common in men; UrthAC and UrthCC are more common in women. Ages were similar in all 4 groups. GA in PIK3CA were the most frequent potentially targetable GA; mTOR pathway GA in PTEN were also identified. GA in other potentially targetable genes were also identified including ERBB2 (6% in UrthUC, 3% in UrthSCC, and 12% in UrthAC), FGFR1-3 (3% in UrthSCC), BRAF (3% in UrthAC), PTCH1 (8% in UrthCC), and MET (8% in UrthCC). Possibly reflecting their higher GA/tumor status, potential for immunotherapy benefit associated with higher tumor mutational burden and PD-L1 staining levels were seen in UrthUC and UrthSCC compared to UrthAC and UrthCC. Microsatellite instability high status was absent throughout. Conclusions Comprehensive genomic profiling reveals GA that may be predictive of both targeted and immunotherapy benefit in patients with advanced UrthCa and that could potentially be used in future adjuvant, neoadjuvant, and metastatic disease trials.
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- 2021
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40. Genomic Features of Metastatic Testicular Sex Cord Stromal Tumors
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Andrea Necchi, Gennady Bratslavsky, Oleg Shapiro, Julia A. Elvin, Jo-Anne Vergilio, Jonathan K. Killian, Nhu Ngo, Shakti Ramkissoon, Eric Severson, Amanda C. Hemmerich, Siraj M. Ali, Jon H. Chung, Prasanth Reddy, Vincent A. Miller, Alexa B. Schrock, Laurie M. Gay, Jeffrey S. Ross, Joseph M. Jacob, Necchi, A, Bratslavsky, G, Shapiro, O, Elvin, Ja, Vergilio, Ja, Killian, Jk, Ngo, N, Ramkissoon, S, Severson, E, Hemmerich, Ac, Ali, Sm, Chung, Jh, Reddy, P, Miller, Va, Schrock, Ab, Gay, Lm, Ross, J, and Jacob, Jm
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Oncology ,Adult ,Male ,medicine.medical_specialty ,Stromal cell ,Adolescent ,Urology ,medicine.medical_treatment ,030232 urology & nephrology ,Malignancy ,Targeted therapy ,Cohort Studies ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Testicular Neoplasms ,CDKN2A ,Internal medicine ,PTEN ,Medicine ,Humans ,Sex Cord-Gonadal Stromal Tumors ,Child ,Testicular cancer ,Aged ,Ovarian Neoplasms ,BAP1 ,Genome ,biology ,business.industry ,Gene Expression Profiling ,Microsatellite instability ,Middle Aged ,medicine.disease ,030220 oncology & carcinogenesis ,biology.protein ,Female ,business - Abstract
Background Metastatic testicular sex cord stromal tumors of the testis (MSCSTs) comprise an extremely uncommon form of genitourinary malignancy. Objective To perform comprehensive genomic profiling (CGP) to enable the search for potential therapy targets. Design, setting, and participants Ten patients with testicular Leydig cell tumors (LCTs), six with Sertoli cell tumors (SCTs), and three with undifferentiated sex cord stromal tumors (USCSTs) and a comparison group of 366 patients with ovarian sex cord stromal tumors (SCSTs) underwent hybrid-capture–based CGP to evaluate all classes of genomic alterations (GAs). The tumor mutational burden (TMB) was determined on 1.1 Mbp of sequenced DNA, and microsatellite instability (MSI) was determined on 114 loci. Intervention CGP on tumor samples. Outcome measurements and statistical analysis Descriptive analyses and differences between histological subgroups were reported. Results and limitations In these patients, all of whom had metastatic disease at the time of sequencing, the primary testis tumor was sequenced in six (32%) patients and a metastatic site in 13 (68%) patients. The overall frequencies of GAs were similar in LCTs, SCTs, and USCSTs, ranging from 3.0 to 3.5 GAs/tumor. The most frequent untargetable GAs included CTNNB1 and CDKN2A/B, both ranging from 20% to 33% of cases. Targetable GAs were uncommon in all MSCST subgroups, but several tumors showed potential for cell-cycle inhibitors (CDK4 in LCTs), mTOR inhibitors (RICTOR, NF2, and PTEN in all three tumor types), hedgehog inhibitors (PTCH1 in LCTs), and poly(ADP-ribose) polymerase inhibitors (BAP1 in SCTs). No MSI-high status was identified. The TMB was also low in all MSCST groups, and tumors featuring a TMB of ≥10 mutations/Mb were not identified. GA findings from ovarian SCSTs largely recapitulated those from MSCSTs. A lack of clinical outcome correlation is a limitation of the present analyses. Conclusions Rare cases of testicular MSCSTs have GAs linked to potential targeted therapy benefits on CGP. In contrast, the lack of MSI-high status and an overall low TMB indicate a likely lack of benefit for immunotherapies. Patient summary Genomic profiling can guide clinical research and disclose therapeutic opportunities for patients with rare testicular cancers for which standard therapies are lacking.
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- 2019
41. Assays to measure small molecule Hsp70 agonist activity in vitro and in vivo.
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Shapiro O, Woods C, Gleixner AM, Sannino S, Ngo M, McDaniels MD, Wipf P, Hukriede NA, Donnelly CJ, and Brodsky JL
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- Animals, Humans, Small Molecule Libraries pharmacology, Small Molecule Libraries chemistry, Optogenetics methods, DNA-Binding Proteins agonists, DNA-Binding Proteins metabolism, HSP70 Heat-Shock Proteins metabolism, HSP70 Heat-Shock Proteins agonists, Zebrafish
- Abstract
Hsp70 prevents protein aggregation and is cytoprotective, but sustained Hsp70 overexpression is problematic. Therefore, we characterized small molecule agonists that augment Hsp70 activity. Because cumbersome assays were required to assay agonists, we developed cell-based and in vivo assays in which disease-associated consequences of Hsp70 activation can be quantified. One assay uses an optogenetic system in which the formation of TDP-43 inclusions can be controlled, and the second assay employs a zebrafish model for acute kidney injury (AKI). These complementary assays will facilitate future work to identify new Hsp70 agonists as well as optimized agonist derivatives., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2025
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42. Role of Cytoreductive Nephrectomy in Metastatic Clear Cell Renal cell Carcinoma in the Era of immunotherapy: An Analysis of the National Cancer Database.
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Zerdan MB, Niforatos S, Arunachalam S, Jamaspishvili T, Wong R, Bratslavsky G, Jacob J, Ross J, Shapiro O, Goldberg H, and Basnet A
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- Humans, Male, Female, Middle Aged, Aged, Databases, Factual, United States, Combined Modality Therapy, Treatment Outcome, Survival Rate, Carcinoma, Renal Cell surgery, Carcinoma, Renal Cell therapy, Carcinoma, Renal Cell pathology, Kidney Neoplasms pathology, Kidney Neoplasms surgery, Kidney Neoplasms therapy, Cytoreduction Surgical Procedures, Nephrectomy methods, Immunotherapy methods
- Abstract
Background: The effectiveness of the clinical outcome of CN (Cytoreductive Nephrectomy) in cases of mccRCC (Metastatic Clear Cell Renal cell Carcinoma) is still uncertain despite two trials, SURTIME and CARMENA. These trials, conducted with Sunitinib as the standard treatment, did not provide evidence supporting the use of CN., Methods: We queried the NCDB for stage IV mccRCC patients between the years of 2004 to 2020, who received (immunotherapy) IO with or without nephrectomy. Overall survival (OS) was calculated among three groups of IO alone, IO followed by CN (IOCN), CN followed by IO (CNIO). Cox models compared OS by treatment group after adjusting for sociodemographic, health, and facility variables., Results: From 1,549,101 renal cancer cases, 7983 clear and nonclear cell renal cell carcinoma cases were identified. After adjusting for sociodemographic and health covariates, patients who received IO followed by CN or CN followed by IO had a respective 64% (adjusted Hazard Ratio [aHR] = 0.36, 95% CI = 0.30-0.43, P = .006] and 47% (aHR = 0.53, 95% CI = 0.49-0.56, P = .001) mortality risk reduction respectively compared to patients who received IO alone. Compared to White adults, individuals who identified as Black exhibited 17% higher risk mortality (aHR = 1.17, 95% CI = 1.06-1.30, P = .002). Patients who received CN prior to IO had a 59% associated mortality risk compared to patients who received IO followed by CN who had a lower risk, 35.7% (P < .001)., Conclusions: Patients receiving CN regardless of sequence with IO did better than IO alone in this national registry-based adjusted analysis for mccRCC. Presently available data indicates that the combination of CN and IO holds promise for enhancing clinical results in patients with mRCC., Competing Interests: Disclosure The authors have stated that they have no conflicts of interest., (Copyright © 2024 Elsevier Inc. All rights reserved.)
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- 2024
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43. Metastasis development in non-muscle-invasive bladder cancer.
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Leyderman M, Chandrasekar T, Grivas P, Li R, Bhat S, Basnet A, Shapiro O, Jacob J, Daneshvar MA, Kord E, Bratslavsky G, and Goldberg H
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Non-muscle-invasive bladder cancer (NMIBC) is the most common type of bladder cancer presentation and is characterized by a varying probability of recurrence and progression. Sporadically, patients with NMIBC might also develop tumour metastases without any pathological evidence of muscle-invasive disease within the bladder, a condition known as metastatic NMIBC. In the published literature, this phenomenon is limited to several case reports and small reviews, with few data regarding the possible aetiologies. Several possible factors can be potentially associated with metastatic NMIBC, including tumour understaging, the number of transurethral resection procedures received by the patient, the presence of circulating tumour cells, the modality used for diagnostic cystoscopy and possible gender-associated differences. In this Perspective, our aim was to integrate and report currently available data on this relatively rare entity and provide some potential aetiological explanations., Competing Interests: Competing interests: The authors declare no competing interests., (© 2024. Springer Nature Limited.)
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- 2024
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44. Disparities Associated with Shared Decision-making in Prostate Cancer Screening.
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Basin MF, Crane K, Basnet A, Chandrasekar T, Shapiro O, Jacob JM, Bratslavsky G, and Goldberg H
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- Humans, Male, Prostate-Specific Antigen analysis, Early Detection of Cancer methods, Cross-Sectional Studies, Retrospective Studies, Decision Making, Mass Screening methods, Prostatic Neoplasms diagnosis, Prostatic Neoplasms prevention & control
- Abstract
Background: Prostate cancer screening guidelines recommend shared decision-making (SDM) regarding prostate-specific antigen (PSA) testing. However, it is unclear who undergoes SDM and whether any disparities exist., Objective: To examine sociodemographic differences in participation of SDM and its association with PSA testing in prostate cancer screening., Design, Setting, and Participants: A retrospective cross-sectional study was conducted among men aged 45-75 yr undergoing PSA screening, using the 2018 National Health Interview Survey database. The evaluated sociodemographic features included age, race, marital status, sexual orientation, smoking status, working status, financial difficulty, US geographic regions, and cancer history. Questions regarding self-reported PSA testing and whether respondents discussed its advantages and disadvantages with their healthcare provider were analyzed., Outcome Measurements and Statistical Analysis: Our primary outcome was to evaluate the possible associations between various sociodemographic factors and undergoing PSA screening and SDM. We used multivariable logistic regression analyses to detect potential associations., Results and Limitations: A total of 59596 men were identified, of whom 5605 answered the question regarding PSA testing, with 2288 (40.6%) undergoing PSA testing. Of these men, 39.5% (n = 2226) discussed the advantages and 25.6% (n = 1434) discussed the disadvantages of PSA testing. On a multivariable analysis, older (odds ratio [OR] 1.092; 95% confidence interval [CI] 1.081-1.103, p < 0.001) and married (OR 1.488; 95% CI 1.287-1.720, p < 0.001) men were more likely to undergo PSA testing. Although Black men were more likely to discuss PSA advantages (OR 1.421; 95% CI 1.150-1.756, p = 0.001) and disadvantages (OR 1.554; 95% CI 1.240-1.947, p < 0.001) than White men, this did not correlate with higher rates of PSA screening (OR 1.086; 95% CI 0.865-1.364, p = 0.477). The lack of important clinical data remains a limitation., Conclusions: Overall, SDM rates were low. Older and married men had an increased likelihood of SDM and PSA testing. Despite higher rates of SDM, Black men had similar rates of PSA testing to White men., Patient Summary: We evaluated sociodemographic differences in shared decision-making (SDM) in prostate cancer screening using a large national database. We found that SDM had varying results in different sociodemographic groups., (Copyright © 2023 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
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- 2023
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45. The association of sexual orientation with prostate, breast, and cervical cancer screening and diagnosis.
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Herriges MJ, Pinkhasov R, Lehavot K, Shapiro O, Jacob JM, Sanford T, Liu N, Bratslavsky G, and Goldberg H
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- Female, Humans, Male, Cross-Sectional Studies, Prostate, Sexual Behavior, Early Detection of Cancer, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Neoplasms epidemiology
- Abstract
Purpose: Data on heterogeneity in cancer screening and diagnosis rates among lesbians/gays and bisexuals (LGBs) is lacking. Recent studies showed that LGBs have decreased healthcare utilization compared to heterosexual counterparts. Few studies have examined how sexual orientation impacts cancer screening and prevalence. We, therefore, investigated the association between sexual orientation and prevalent sex-specific cancer including prostate (PCa), breast (BC), and cervical (CC) cancer., Methods: This was a cross-sectional survey-based US study, including men and women aged 18 + from the Health Information National Trends Survey (HINTS) database between 2017 and 2019. The primary endpoint was individual-reported prostate, breast, and cervical cancer screening and prevalence rates among heterosexual and LGB men and women. Multivariable logistic regression analyses assessed association of various covariates with undergoing screening and diagnosis of these cancers., Results: Overall, 4,441 and 6,333 heterosexual men and women, respectively, were compared to 225 and 213 LGB men and women, respectively. LGBs were younger and less likely to be screened for PCa, BC, and CC than heterosexuals. A higher proportion of heterosexual women than lesbian and bisexual women were screened for CC with pap smears (95.36% vs. 90.48% and 86.11%, p ≤ 0.001) and BC with mammograms (80.74% vs. 63.81% and 45.37%, p ≤ 0.001). Similarly, a higher proportion of heterosexual men than gay and bisexual men were screened for PCa with PSA blood tests (41.27% vs. 30.53% and 27.58%, p ≤ 0.001)., Conclusion: There were more heterosexuals than LGBs screened for CC, BC, and PCa. However, no association between sexual orientation and cancer diagnosis was found. Healthcare professionals should be encouraged to improve cancer screening among LGBs., (© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
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- 2022
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46. Financial Toxicity and Its Association With Prostate and Colon Cancer Screening.
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Herriges MJ, Shenhav-Goldberg R, Peck JI, Bhanvadia SK, Morgans A, Chino F, Chandrasekar T, Shapiro O, Jacob JM, Basnet A, Bratslavsky G, and Goldberg H
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- Cross-Sectional Studies, Early Detection of Cancer, Financial Stress, Humans, Male, Mass Screening, Prostate, Prostate-Specific Antigen, Colonic Neoplasms diagnosis, Colonic Neoplasms epidemiology, Prostatic Neoplasms diagnosis, Prostatic Neoplasms epidemiology
- Abstract
Background: The term "financial toxicity" or "hardship" is a patient-reported outcome that results from the material costs of cancer care, the psychological impacts of these costs, and the coping strategies that patients use to deal with the strain that includes delaying or forgoing care. However, little is known about the impact of financial toxicity on cancer screening. We examined the effects of financial toxicity on the use of screening tests for prostate and colon cancer. We hypothesized that greater financial hardship would show an association with decreased prevalence of cancer screening., Methods: This cross-sectional survey-based US study included men and women aged ≥50 years from the National Health Interview Survey database from January through December 2018. A financial hardship score (FHS) between 0 and 10 was formulated by summarizing the responses from 10 financial toxicity dichotomic questions (yes or no), with a higher score associated with greater financial hardship. Primary outcomes were self-reported occurrence of prostate-specific antigen (PSA) blood testing and colonoscopy for prostate and colon cancer screening, respectively., Results: Overall, 13,439 individual responses were collected. A total of 9,277 (69.03%) people had undergone colonoscopies, and 3,455 (70.94%) men had a PSA test. White, married, working men were more likely to undergo PSA testing and colonoscopy. Individuals who had not had a PSA test or colonoscopy had higher mean FHSs than those who underwent these tests (0.70 and 0.79 vs 0.47 and 0.61, respectively; P≤.001 for both). Multivariable logistic regression models demonstrated that a higher FHS was associated with a decreased odds ratio for having a PSA test (0.916; 95% CI, 0.867-0.967; P=.002) and colonoscopy (0.969; 95% CI, 0.941-0.998; P=.039)., Conclusions: Greater financial hardship is suggested to be associated with a decreased probability of having prostate and colon cancer screening. Healthcare professionals should be aware that financial toxicity can impact not only cancer treatment but also cancer screening.
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- 2022
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47. Prostate-specific Antigen Testing in Men with Disabilities: A Cross-sectional Analysis of the Health Information National Trends Survey.
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Leong JY, Pinkhasov R, Chandrasekar T, Shapiro O, Daneshvar M, Jacob J, Sanford T, Bratslavsky G, and Goldberg H
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- Male, Humans, Prostate-Specific Antigen, Cross-Sectional Studies, Early Detection of Cancer methods, Prostatic Neoplasms diagnosis, Prostatic Neoplasms epidemiology, Persons with Disabilities
- Abstract
Background: Patients with disabilities represent a unique minority population. The incidence of prostate-specific antigen (PSA) testing among this population is unknown., Objective: To compare PSA testing rates and associated predictors among men with and without reported disabilities in the USA., Design, Setting, and Participants: A cross-sectional study of the Health Information National Trends Survey (HINTS) for the years 2012, 2013, 2017 and 2019 was conducted in men with reported disabilities., Outcome Measurements and Statistical Analysis: Baseline demographics of the entire cohort were stratified based on their reported disabilities (none, disabled, deaf, and blind). Each disability was compared separately and in combination with the cohort without disabilities. Multivariable logistic regression models determined clinically significant predictors of PSA testing in men with disabilities compared with those without., Results and Limitations: Overall, 782 (15%) men with disabilities were compared with 4569 (85%) men without disabilities. The former cohort was older with a median (interquartile range) age of 65 (56-75) versus 57 (43-67) yr (p < 0.001). On multivariable analysis, men with any disability were less likely to undergo PSA testing (odds ratio 0.77, 95% confidence interval 0.62-0.96, p = 0.018). Variables associated with increased PSA testing included age, having a health care provider, health insurance, and living with a partner., Conclusions: Inequalities in PSA testing exist among men with disabilities in the USA, especially among the deaf and blind, being less likely to undergo PSA testing. Further research is required to identify and deal with any obstacles in the implementation of equal PSA testing in this unique population., Patient Summary: In the USA, men with reported disabilities are less likely to undergo PSA testing than patients without reported disabilities., (Copyright © 2021 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
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- 2022
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48. Risk Behaviors, Family Support, and Emotional Health among Adolescents during the COVID-19 Pandemic in Israel.
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Shapiro O, Gannot RN, Green G, Zigdon A, Zwilling M, Giladi A, Ben-Meir L, Adilson M, Barak S, Harel-Fisch Y, and Tesler R
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- Adolescent, Child, Communicable Disease Control, Humans, Israel epidemiology, Pandemics, Risk-Taking, Adolescent Behavior psychology, Binge Drinking, COVID-19 epidemiology
- Abstract
We investigated the prevalence of risk behaviors among Israeli adolescents (tobacco smoking, alcohol consumption, drug use) during the COVID-19 pandemic. Associations between different risk behaviors were examined and so was whether specific characteristics could predict risk behaviors in adolescents. The study consisted of 1020 Israeli adolescents aged 15-18. Study subjects completed an online survey between the first and second lockdowns in Israel (April 2020 to September 2020). Participants reported the frequency at which they engaged in four different risky behaviors: general risky behavior, tobacco smoking, alcohol consumption (binge drinking), and cannabis use. The most prevalent risky behavior in the sample was binge drinking (33.8%). The four measured risky behaviors were significantly correlated. Among participants who had previously engaged in a risky behavior assessed, most did not change the behavior frequency during the pandemic. All independent variables (sociodemographic characteristics, family support, and emotional, health excluding friends' support, physical activity volume, and coronavirus restrictions) were significantly different between participants engaging vs. not engaging in risky behaviors. Our findings suggest that family support is one of the most influential factors in preventing risky behavior during the pandemic, and they emphasize the importance of family-based interventions with children and adolescents from elementary to high school.
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- 2022
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49. Association of Race With Cancer-Related Financial Toxicity.
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Panzone J, Welch C, Morgans A, Bhanvadia SK, Mossanen M, Shenhav-Goldberg R, Chandrasekar T, Pinkhasov R, Shapiro O, Jacob JM, Basnet A, Bratslavsky G, and Goldberg H
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- Cross-Sectional Studies, Female, Hispanic or Latino, Humans, Male, White People, Financial Stress, Neoplasms
- Abstract
Purpose: We investigated the association between race and FT among previous patients with cancer. Studies show that patients with cancer experience financial toxicity (FT) because of their cancer treatment., Methods: Data on individuals with a cancer history were collected in this cross-sectional study during 2012, 2014, and 2017, from the US Health Information National Trends Survey. This survey is conducted by mail with monetary compensation as an incentive. We specifically assessed responses to two questions: Has cancer hurt you financially? Have you been denied health insurance because of cancer? Multivariable logistic regression analyses were used to assess the associations between these questions and race., Results: Of 10,592 individuals participating, 1,328 men and women (12.5%) with a cancer history were assessed. Compared with Blacks, Whites were found to have a higher rate of insurance (95.4% v 90.0%), were more likely to receive cancer treatment (93.9% v 85%), and had a higher rate of surgical treatment than Blacks (77% v 60%), Hispanics (55%), and others (77%, 60%, 55%, and 74.2%, respectively, P < .001). On multivariable analysis, Blacks were more than five times as likely to be denied insurance (odds ratio, 5.003; 95% CI, 2.451 to 10.213; P < .001) and more than twice as likely to report being hurt financially because of cancer (odds ratio, 2.448; 95% CI, 1.520 to 3.941; P < .001) than Whites. Of all cancer groups analyzed (genitourinary, gynecologic, gastrointestinal, and breast), genitourinary malignancies were the only group in which the rate of reporting being hurt financially varied in a statistically significant manner (Whites 36.7%, Hispanics 62.5%, and Blacks 59.3%, P = .004)., Conclusion: Our data suggest that race is significantly associated with FT because of cancer. Awareness of racial inequality with regards to FT should be raised among health care workers., Competing Interests: Christopher WelchEmployment: St Lukes Hospital (I) Alicia MorgansHonoraria: Genentech, Janssen, Sanofi, AstraZeneca, Astellas Scientific and Medical Affairs Inc, Astellas Pharma, Janssen Oncology, Bayer, Clovis Oncology, Myovant Sciences, Advanced Accelerator Applications, Exelixis, Pfizer, MerckConsulting or Advisory Role: AstraZeneca, Sanofi, Bayer, Astellas Pharma, Janssen, Advanced Accelerator Applications, Myovant Sciences, Blue Earth Diagnostics, Exelixis, Novartis, Myriad Genetics, Lantheus Medical Imaging, MerckResearch Funding: Bayer, Seattle Genetics/Astellas, Genentech, AstraZeneca, Astellas Scientific and Medical Affairs Inc, Dendreon, Sanofi, Myovant SciencesTravel, Accommodations, Expenses: Sanofi Sumeet K. BhanvadiaEmployment: Advantage Health Care Services (I)Stock and Other Ownership Interests: Johnson and JohnsonTravel, Accommodations, Expenses: Intuitive Surgical, Cysview Matthew MossanenOther Relationship: Elsevier Oleg ShapiroStock and Other Ownership Interests: Verve Medical Joseph M. JacobConsulting or Advisory Role: Verity Pharmaceuticals, Photocure Gennady BratslavskyEmployment: AptametrixLeadership: Taurus DiagnosticsStock and Other Ownership Interests: Ilgen, RespiquestConsulting or Advisory Role: Novartis, Johnson & Johnson/Janssen Hanan GoldbergConsulting or Advisory Role: Myovant SciencesNo other potential conflicts of interest were reported.
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- 2022
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50. Is There a Role for Prone Computed Tomography Before Percutaneous Nephrolithotomy?
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LaBella D, Pinkhasov A, Sanford T, Shapiro O, and Wiener S
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- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Patient Positioning methods, Pilot Projects, Prone Position, Supine Position, Tomography, X-Ray Computed, Kidney Calculi diagnostic imaging, Kidney Calculi surgery, Nephrolithotomy, Percutaneous, Nephrostomy, Percutaneous methods
- Abstract
Background: The majority of percutaneous nephrolithotomies (PCNLs) are performed prone, whereas most preoperative CT scans are done supine. The purpose of this pilot study is to determine if there is utility of prone CT scans in preoperative planning for prone PCNL by identifying patient populations at risk for organ injury and tract length-related complications. Materials and Methods: To represent typical preoperative planning using CT, two-dimensional (2D)-axial-prone/supine percutaneous tract measurements were performed by minimizing the distance from the target calix to the posterior-lateral skin in a single axial plane. The minimum distance and organ interception rates for the 2D-axial planning scans were recorded. Results: A total of 60 CT colonography and 13 CT urography patients were included in analysis. There were 42 women and 31 men with unspecified pathology reports ranging in age from 27 to 86 years and in body mass index (BMI) from 17.1 to 49. Multiple logistic regression identified female gender and low BMI as predictors of organ interception on the left. On multiple linear regression comparing the difference in axial prone/supine lengths; BMI, gender, and age were not significant independent predictors of changes in tract length in any pole when prone vs supine. However, shorter supine tracts tended to lengthen when prone, and longer supine tracts tended to shorten. Conclusions: This pilot study has demonstrated that patients with long and short estimates of tract length in the supine position may have shorter and longer tracts, respectively, with repositioning to prone. Thus, prone CT may have benefit when anticipating exceptionally long (>15 cm) tract lengths. Prone scans also revealed more potential organ interceptions, particularly for low BMI and women in the left upper pole. In patients for whom prone CT demonstrates an organ interception, the urologist should consider an alternate target calix or ultrasound-guided percutaneous access to identify the most appropriate needle trajectory.
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- 2022
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