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Carbon nanospheres mediated nuclear delivery of SMAR1 protein (DNA binding domain) controls breast tumor in mice model.
- Source :
-
Nanomedicine (London, England) [Nanomedicine (Lond)] 2018 Feb; Vol. 13 (4), pp. 353-372. Date of Electronic Publication: 2018 Jan 17. - Publication Year :
- 2018
-
Abstract
- Aim: To investigate anticancer activity of the DNA binding domain of SMAR1 (His 5) in vitro and in vivo.<br />Materials & Methods: His 5 was conjugated to hydrothermally synthesized carbon nanospheres (CNs). Anticancer activity of CNs-His 5 was evaluated in vitro and in vivo.<br />Results: CNs- His 5 significantly reduced cyclin D1 levels in MDA-MB-231 cells. Tumor bearing Balb/c mice injected with CNs-His 5 showed approximately 62% tumor regression and significantly reduced <superscript>18</superscript> FDG uptake. Caspases assay and IHC staining confirmed tumor growth inhibition, which could be attributed to apoptotic, antiproliferative and antiangiogenic activities of His 5.<br />Conclusion: DNA binding domain of the SMAR1 protein (His 5) has potent anticancer activity and its CNs mediated delivery could control breast tumor in mice model.
- Subjects :
- Animals
Antineoplastic Agents administration & dosage
Apoptosis drug effects
Cell Cycle Proteins metabolism
Cell Line, Tumor
Cell Survival drug effects
Cyclin D1 metabolism
DNA-Binding Proteins metabolism
Drug Liberation
Female
Humans
Mice, Inbred BALB C
Nuclear Proteins metabolism
Protein Domains
Recombinant Proteins administration & dosage
Tissue Distribution
Antineoplastic Agents chemistry
Breast Neoplasms drug therapy
Carbon chemistry
Cell Cycle Proteins administration & dosage
DNA-Binding Proteins administration & dosage
Drug Carriers chemistry
Nanospheres chemistry
Nuclear Proteins administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1748-6963
- Volume :
- 13
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Nanomedicine (London, England)
- Publication Type :
- Academic Journal
- Accession number :
- 29338617
- Full Text :
- https://doi.org/10.2217/nnm-2017-0298