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2. Author Correction: The NK cell granule protein NKG7 regulates cytotoxic granule exocytosis and inflammation

Author

Ng, Susanna S., De Labastida Rivera, Fabian, Yan, Juming, Corvino, Dillon, Das, Indrajit, Zhang, Ping, Kuns, Rachel, Chauhan, Shashi Bhushan, Hou, Jiajie, Li, Xian-Yang, Frame, Teija C. M., McEnroe, Benjamin A., Moore, Eilish, Na, Jinrui, Engel, Jessica A., Soon, Megan S. F., Singh, Bhawana, Kueh, Andrew J., Herold, Marco J., Montes de Oca, Marcela, Singh, Siddharth Sankar, Bunn, Patrick T., Aguilera, Amy Roman, Casey, Mika, Braun, Matthias, Ghazanfari, Nazanin, Wani, Shivangi, Wang, Yulin, Amante, Fiona H., Edwards, Chelsea L., Haque, Ashraful, Dougall, William C., Singh, Om Prakash, Baxter, Alan G., Teng, Michele W. L., Loukas, Alex, Daly, Norelle L., Cloonan, Nicole, Degli-Esposti, Mariapia A., Uzonna, Jude, Heath, William R., Bald, Tobias, Tey, Siok-Keen, Nakamura, Kyohei, Hill, Geoffrey R., Kumar, Rajiv, Sundar, Shyam, Smyth, Mark J., and Engwerda, Christian R.

Published
2024
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4. RANK and RANKL Expression in Tumors of Patients with Early Breast Cancer

Author

Behrens, Annika, primary, Wurmthaler, Lena, primary, Heindl, Felix, additional, Gass, Paul, additional, Häberle, Lothar, additional, Volz, Bernhard, additional, Hack, Carolin C., additional, Emons, Julius, additional, Erber, Ramona, additional, Hartmann, Arndt, additional, Beckmann, Matthias W., additional, Ruebner, Matthias, additional, Dougall, William C., additional, Fasching, Peter A., additional, Huebner, Hanna, additional, and Press, Michael F., additional

Published
2024
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5. The NK cell granule protein NKG7 regulates cytotoxic granule exocytosis and inflammation

Author

Ng, Susanna S., De Labastida Rivera, Fabian, Yan, Juming, Corvino, Dillon, Das, Indrajit, Zhang, Ping, Kuns, Rachel, Chauhan, Shashi Bhushan, Hou, Jiajie, Li, Xian-Yang, Frame, Teija C. M., McEnroe, Benjamin A., Moore, Eilish, Na, Jinrui, Engel, Jessica A., Soon, Megan S. F., Singh, Bhawana, Kueh, Andrew J., Herold, Marco J., Montes de Oca, Marcela, Singh, Siddharth Sankar, Bunn, Patrick T., Aguilera, Amy Roman, Casey, Mika, Braun, Matthias, Ghazanfari, Nazanin, Wani, Shivangi, Wang, Yulin, Amante, Fiona H., Edwards, Chelsea L., Haque, Ashraful, Dougall, William C., Singh, Om Prakash, Baxter, Alan G., Teng, Michele W. L., Loukas, Alex, Daly, Norelle L., Cloonan, Nicole, Degli-Esposti, Mariapia A., Uzonna, Jude, Heath, William R., Bald, Tobias, Tey, Siok-Keen, Nakamura, Kyohei, Hill, Geoffrey R., Kumar, Rajiv, Sundar, Shyam, Smyth, Mark J., and Engwerda, Christian R.

Published
2020
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6. RANK and RANKL Expression in Tumors of Patients with Early Breast Cancer

Author

Behrens, Annika, primary, Wurmthaler, Lena, primary, Heindl, Felix, additional, Gass, Paul, additional, Häberle, Lothar, additional, Volz, Bernhard, additional, Hack, Carolin C., additional, Emons, Julius, additional, Erber, Ramona, additional, Hartmann, Arndt, additional, Beckmann, Matthias W., additional, Ruebner, Matthias, additional, Dougall, William C., additional, Press, Michael F., additional, Fasching, Peter A., additional, and Huebner, Hanna, additional

Published
2023
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7. NMDAR antagonists suppress tumor progression by regulating tumor-associated macrophages

Author

Yuan, Dongchen, primary, Hu, Jing, additional, Ju, Xiaoman, additional, Putz, Eva Maria, additional, Zheng, Simin, additional, Koda, Stephane, additional, Sun, Guowei, additional, Deng, Xiaoran, additional, Xu, Zhipeng, additional, Nie, Wei, additional, Zhao, Yang, additional, Li, Xianyang, additional, Dougall, William C., additional, Shao, Simin, additional, Chen, Yan, additional, Tang, Renxian, additional, Zheng, Kuiyang, additional, and Yan, Juming, additional

Published
2023
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8. Retraction: CD155 loss enhances tumor suppression via combined host and tumor-intrinsic mechanisms

Author

Li, Xian-Yang, Das, Indrajit, Lepletier, Ailin, Addala, Venkateswar, Bald, Tobias, Stannard, Kimberley, Barkauskas, Deborah, Liu, Jing, Aguilera, Amelia Roman, Takeda, Kazuyoshi, Braun, Matthias, Nakamura, Kyohei, Jacquelin, Sebastien, Lane, Steven W., Teng, Michele W.L., Dougall, William C., and Smyth, Mark J.

Subjects
Health care industry
Abstract

Original citation: J Clin Invest. 2018;128(6):2613-2625. https://doi.org/10.1172/JCI98769. Citation for this retraction: J Clin Invest. 2022;132(6):e159825. https://doi.org/10.1172/JCI159825. QIMR Berghofer Medical Research Institute recently notified the JCI of concerns regarding Figures 4I [...]

Published
2022
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11. CD155 loss enhances tumor suppression via combined host and tumor-intrinsic mechanisms

Author

Li, Xian-Yang, Das, Indrajit, Lepletier, Ailin, Addala, Venkateswar, Bald, Tobias, Stannard, Kimberley, Barkauskas, Deborah, Liu, Jing, Aguilera, Amelia Roman, Takeda, Kazuyoshi, Braun, Matthias, Nakamura, Kyohei, Jacquelin, Sebastien, Lane, Steven W., Teng, Michele W.L., Dougall, William C., and Smyth, Mark J.

Subjects
Cancer treatment -- Research, Cancer research, Immunosuppression -- Research, Virus receptors -- Health aspects, Immunoglobulins -- Health aspects, Health care industry
Abstract

Critical immune-suppressive pathways beyond programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) require greater attention. Nectins and nectin-like molecules might be promising targets for immunotherapy, since they play critical roles in cell proliferation and migration and exert immunomodulatory functions in pathophysiological conditions. Here, we show CD155 expression in both malignant cells and tumor-infiltrating myeloid cells in humans and mice. [Cd155.sup.-/-] mice displayed reduced tumor growth and metastasis via DNAM-1 upregulation and enhanced effector function of [CD8.sup.+] T and NK cells, respectively. CD155-deleted tumor cells also displayed slower tumor growth and reduced metastases, demonstrating the importance of a tumor-intrinsic role of CD155. CD155 absence on host and tumor cells exerted an even greater inhibition of tumor growth and metastasis. Blockade of PD-1 or both PD-1 and CTLA4 was more effective in settings in which CD155 was limiting, suggesting the clinical potential of cotargeting PD-L1 and CD155 function., Introduction Immunotherapy is emerging as an alternative to standard anti-cancer therapies, with the successful treatment of a proportion of various advanced cancer patients with anti-programmed death 1 (anti-PD-1), anti-programmed death [...]

Published
2018
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13. Supplementary Data from CD96 Is an Immune Checkpoint That Regulates CD8+ T-cell Antitumor Function

Author

Mittal, Deepak, primary, Lepletier, Ailin, primary, Madore, Jason, primary, Aguilera, Amelia Roman, primary, Stannard, Kimberley, primary, Blake, Stephen J., primary, Whitehall, Vicki L.J., primary, Liu, Cheng, primary, Bettington, Mark L., primary, Takeda, Kazuyoshi, primary, Long, Georgina V., primary, Scolyer, Richard A., primary, Lan, Ruth, primary, Siemers, Nathan, primary, Korman, Alan, primary, Teng, Michele W.L., primary, Johnston, Robert J., primary, Dougall, William C., primary, and Smyth, Mark J., primary

Published
2023
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14. Supplementary Methods and Legends from CD96 Is an Immune Checkpoint That Regulates CD8+ T-cell Antitumor Function

Author

Mittal, Deepak, primary, Lepletier, Ailin, primary, Madore, Jason, primary, Aguilera, Amelia Roman, primary, Stannard, Kimberley, primary, Blake, Stephen J., primary, Whitehall, Vicki L.J., primary, Liu, Cheng, primary, Bettington, Mark L., primary, Takeda, Kazuyoshi, primary, Long, Georgina V., primary, Scolyer, Richard A., primary, Lan, Ruth, primary, Siemers, Nathan, primary, Korman, Alan, primary, Teng, Michele W.L., primary, Johnston, Robert J., primary, Dougall, William C., primary, and Smyth, Mark J., primary

Published
2023
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15. Data from CD96 Is an Immune Checkpoint That Regulates CD8+ T-cell Antitumor Function

Author

Mittal, Deepak, primary, Lepletier, Ailin, primary, Madore, Jason, primary, Aguilera, Amelia Roman, primary, Stannard, Kimberley, primary, Blake, Stephen J., primary, Whitehall, Vicki L.J., primary, Liu, Cheng, primary, Bettington, Mark L., primary, Takeda, Kazuyoshi, primary, Long, Georgina V., primary, Scolyer, Richard A., primary, Lan, Ruth, primary, Siemers, Nathan, primary, Korman, Alan, primary, Teng, Michele W.L., primary, Johnston, Robert J., primary, Dougall, William C., primary, and Smyth, Mark J., primary

Published
2023
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16. Supplementary Methods and References from RANK Signaling Blockade Reduces Breast Cancer Recurrence by Inducing Tumor Cell Differentiation

Author

Yoldi, Guillermo, primary, Pellegrini, Pasquale, primary, Trinidad, Eva M., primary, Cordero, Alex, primary, Gomez-Miragaya, Jorge, primary, Serra-Musach, Jordi, primary, Dougall, William C., primary, Muñoz, Purificación, primary, Pujana, Miguel-Angel, primary, Planelles, Lourdes, primary, and González-Suárez, Eva, primary

Published
2023
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17. Supplementary Figure 1 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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18. Supplementary Figure S3 from RANK Signaling Blockade Reduces Breast Cancer Recurrence by Inducing Tumor Cell Differentiation

Author

Yoldi, Guillermo, primary, Pellegrini, Pasquale, primary, Trinidad, Eva M., primary, Cordero, Alex, primary, Gomez-Miragaya, Jorge, primary, Serra-Musach, Jordi, primary, Dougall, William C., primary, Muñoz, Purificación, primary, Pujana, Miguel-Angel, primary, Planelles, Lourdes, primary, and González-Suárez, Eva, primary

Published
2023
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19. Supplementary Table S1 from RANK Signaling Blockade Reduces Breast Cancer Recurrence by Inducing Tumor Cell Differentiation

Author

Yoldi, Guillermo, primary, Pellegrini, Pasquale, primary, Trinidad, Eva M., primary, Cordero, Alex, primary, Gomez-Miragaya, Jorge, primary, Serra-Musach, Jordi, primary, Dougall, William C., primary, Muñoz, Purificación, primary, Pujana, Miguel-Angel, primary, Planelles, Lourdes, primary, and González-Suárez, Eva, primary

Published
2023
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20. Supplementary Figure 7 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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22. Supplementary Figure 5 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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23. Supplementary Methods, Figure Legends 1-7 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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24. Data from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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25. Supplementary Figure 3 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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26. Supplementary Figure 4 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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27. Supplementary Figure 2 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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28. Supplementary Table and Figure Legends from RANK Signaling Blockade Reduces Breast Cancer Recurrence by Inducing Tumor Cell Differentiation

Author

Yoldi, Guillermo, primary, Pellegrini, Pasquale, primary, Trinidad, Eva M., primary, Cordero, Alex, primary, Gomez-Miragaya, Jorge, primary, Serra-Musach, Jordi, primary, Dougall, William C., primary, Muñoz, Purificación, primary, Pujana, Miguel-Angel, primary, Planelles, Lourdes, primary, and González-Suárez, Eva, primary

Published
2023
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29. Supplementary Figure 6 from RANK Induces Epithelial–Mesenchymal Transition and Stemness in Human Mammary Epithelial Cells and Promotes Tumorigenesis and Metastasis

Author

Palafox, Marta, primary, Ferrer, Irene, primary, Pellegrini, Pasquale, primary, Vila, Sergi, primary, Hernandez-Ortega, Sara, primary, Urruticoechea, Ander, primary, Climent, Fina, primary, Soler, Maria Teresa, primary, Muñoz, Purificación, primary, Viñals, Francesc, primary, Tometsko, Mark, primary, Branstetter, Dan, primary, Dougall, William C., primary, and González-Suárez, Eva, primary

Published
2023
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30. New Targeted Therapies for Bone Metastases

Author

Lipton, Allan, Costa, Luis, Sieber, Paul, Dougall, William C., Braun, Ada, Ablin, Richard J., Series editor, Jiang, Wen G., Series editor, Vassiliou, Vassilios, editor, Chow, Edward, editor, and Kardamakis, Dimitrios, editor

Published
2014
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31. NMDAR antagonists suppress tumor progression by regulating tumor-associated macrophages.

Author

Dongchen Yuan, Jing Hu, Xiaoman Ju, Putz, Eva Maria, Simin Zheng, Koda, Stephane, Guowei Sun, Xiaoran Deng, Zhipeng Xu, Wei Nie, Yang Zhao, Xianyang Li, Dougall, William C., Simin Shao, Yan Chen, Renxian Tang, Kuiyang Zheng, and Juming Yan

Subjects
CANCER invasiveness, MACROPHAGES, NEUROTRANSMITTER receptors, METHYL aspartate receptors, LIVER tumors
Abstract

Neurotransmitter receptors are increasingly recognized to play important roles in anti-tumor immunity. The expression of the ion channel N-methyl-D-aspartate receptor (NMDAR) on macrophages was reported, but the role of NMDAR on macrophages in the tumor microenvironment (TME) remains unknown. Here, we show that the activation of NMDAR triggered calcium influx and reactive oxygen species production, which fueled immunosuppressive activities in tumor-associated macrophages (TAMs) in the hepatocellular sarcoma and fibrosarcoma tumor settings. NMDAR antagonists, MK-801, memantine, and magnesium, effectively suppressed these processes in TAMs. Single-cell RNA sequencing analysis revealed that blocking NMDAR functionally and metabolically altered TAM phenotypes, such that they could better promote T cell-and Natural killer (NK) cell-mediated anti-tumor immunity. Treatment with NMDAR antagonists in combination with anti-PD-1 antibody led to the elimination of the majority of established preclinical liver tumors. Thus, our study uncovered an unknown role for NMDAR in regulating macrophages in the TME of hepatocellular sarcoma and provided a rationale for targeting NMDAR for tumor immunotherapy. [ABSTRACT FROM AUTHOR]

Published
2023
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33. Inhibition of CD39 unleashes macrophage antibody-dependent cellular phagocytosis against B-cell lymphoma

Author

Casey, Mika, primary, Segawa, Kane, additional, Law, Soi Cheng, additional, Sabdia, Muhamamed Bilal, additional, Nowlan, Bianca, additional, Salik, Basit, additional, Lee, Carol, additional, Winterford, Clay, additional, Pearson, Sally, additional, Madore, Jason, additional, Dougall, William C., additional, Gandhi, Maher K., additional, and Nakamura, Kyohei, additional

Published
2022
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35. Inhibition of leukemia cell engraftment and disease progression in mice by osteoblasts

Author

Krevvata, Maria, Silva, Barbara C., Manavalan, John S., Galan-Diez, Marta, Kode, Aruna, Matthews, Brya Grace, Park, David, Zhang, Chiyuan A., Galili, Naomi, Nickolas, Thomas L., Dempster, David W., Dougall, William, Teruya-Feldstein, Julie, Economides, Aris N., Kalajzic, Ivo, Raza, Azra, Berman, Ellin, Mukherjee, Siddhartha, Bhagat, Govind, and Kousteni, Stavroula

Published
2014
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39. RANK ligand as a potential target for breast cancer prevention in BRCA1-mutation carriers

Author

Nolan, Emma, Vaillant, Francois, Branstetter, Daniel, Pal, Bhupinder, Giner, Goknur, Whitehead, Lachlan, Lok, Sheau W., Mann, Gregory B., Rohrbach, Kathy, Huang, Li-Ya, Soriano, Rosalia, Smyth, Gordon K., Dougall, William C., Visvader, Jane E., and Lindeman, Geoffrey J.

Subjects
Cytokines -- Health aspects, Breast cancer -- Genetic aspects -- Development and progression -- Care and treatment, BRCA mutations -- Health aspects, Biological sciences, Health
Abstract

Individuals who have mutations in the breast-cancer-susceptibility gene BRCA1 (hereafter referred to as BRCAl-mutation carriers) frequently undergo prophylactic mastectomy to minimize their risk of breast cancer. The identification of an effective prevention therapy therefore remains a 'holy grail' for the field. Precancerous [BRCA1.sup.mut/+] tissue harbors an aberrant population of luminal progenitor cells (1), and deregulated progesterone signaling has been implicated in BRCAl-associated oncogenesis (2-5). Coupled with the findings that tumor necrosis factor superfamily member 11 (TNFSF11; also known as RANKL) is a key paracrine effector of progesterone signaling (6-10) and that RANKL and its receptor TNFRSF11A (also known as RANK) contribute to mammary tumorigenesis (11-13), we investigated a role for this pathway in the pre-neoplastic phase of BRCAl-mutation carriers. We identified two subsets of luminal progenitors ([RANK.sup.+] and [RANK.sup.-]) in histologically normal tissue of BRCAl-mutation carriers and showed that [RANK.sup.+] cells are highly proliferative, have grossly aberrant DNA repair and bear a molecular signature similar to that of basal-like breast cancer. These data suggest that [RANK.sup.+] and not [RANK.sup.-] progenitors are a key target population in these women. Inhibition of RANKL signaling by treatment with denosumab in three-dimensional breast organoids derived from pre-neoplastic [BRCA1.sup.mut/+] tissue attenuated progesterone-induced proliferation. Notably, proliferation was markedly reduced in breast biopsies from BRCAl-mutation carriers who were treated with denosumab. Furthermore, inhibition of RANKL in a Brcal-deficient mouse model substantially curtailed mammary tumorigenesis. Taken together, these findings identify a targetable pathway in a putative cell-of-origin population in BRCAl-mutation carriers and implicate RANKL blockade as a promising strategy in the prevention of breast cancer., Women who harbor germline mutations in BRCA1 have an approximately 65% cumulative risk of developing breast cancer by age 70 (ref. 14). Breast tumors often arise at an early age, [...]

Published
2016

42. CD155 loss enhances tumor suppression via combined host and tumor-intrinsic mechanisms

Author

Li, Xian-Yang, primary, Das, Indrajit, additional, Lepletier, Ailin, additional, Addala, Venkateswar, additional, Bald, Tobias, additional, Stannard, Kimberley, additional, Barkauskas, Deborah, additional, Liu, Jing, additional, Aguilera, Amelia Roman, additional, Takeda, Kazuyoshi, additional, Braun, Matthias, additional, Nakamura, Kyohei, additional, Jacquelin, Sebastien, additional, Lane, Steven W., additional, Teng, Michele W.L., additional, Dougall, William C., additional, and Smyth, Mark J., additional

Published
2022
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