Combined gossypol and zoledronic acid treatment results in synergistic induction of cell death and regulates angiogenic molecules in ovarian cancer cells
dc.contributor.author | Atmaca H. | |
dc.contributor.author | Gorumlu G. | |
dc.contributor.author | Karaca B. | |
dc.contributor.author | Degirmenci M. | |
dc.contributor.author | Tunali D. | |
dc.contributor.author | Cirak Y. | |
dc.contributor.author | Purcu D.U. | |
dc.contributor.author | Uzunoglu S. | |
dc.contributor.author | Karabulut B. | |
dc.contributor.author | Sanli U.A. | |
dc.contributor.author | Uslu R. | |
dc.date.accessioned | 2024-07-22T08:21:14Z | |
dc.date.available | 2024-07-22T08:21:14Z | |
dc.date.issued | 2009 | |
dc.description.abstract | In the present study, we aimed to evaluate the possible synergistic, cytotoxic effects of combination treatment of gossypol and zoledronic acid, in human ovarian cancer cell lines, OVCAR-3 and MDAH-2774, and to elucidate the role of this novel combination treatment on angiogenesis-related molecules in ovarian cancer. The XTT cell viability assay was used for showing cytotoxicity. Both DNA fragmentation by ELISA assay and caspase 3/7 activity measurement were used for demonstrating apoptosis. To elucidate the angiogenic molecules affected by combination treatment, mRNA levels of angiogenic molecules were measured using the Human Angiogenesis RT2 Profiler™ PCR Array (SuperArray, Frederick, MD) in ovarian cancer cell lines, OVCAR-3 and MDAH-2774.The combined treatment resulted in significant, synergistic cytotoxicity, and induced apoptosis. This effect was observed to happen in a dose- and time-dependent manner. Moreover, the combination treatment of 10 μM gossypol and 5 μM zoledronic acid resulted in significant down-regulation (≥ thee-fold) in mRNA levels of some pivotal angiogenic molecules in OVCAR-3 and MDAH-2774 cells as compared to the untreated control. However, this effect was different in the two ovarian cancer cell lines observed. Gossypol, in combination with zoledronic acid, may provide a rational treatment option for ovarian cancer, not only by direct inhibition of cell proliferation, but also inhibition of angiogenesis-related molecules. | |
dc.identifier.DOI-ID | 10.1684/ecn.2009.0159 | |
dc.identifier.issn | 11485493 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18522 | |
dc.language.iso | English | |
dc.subject | Angiogenesis Inducing Agents | |
dc.subject | Caspase 3 | |
dc.subject | Caspase 7 | |
dc.subject | Cell Death | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cell Proliferation | |
dc.subject | Diphosphonates | |
dc.subject | DNA Fragmentation | |
dc.subject | Down-Regulation | |
dc.subject | Drug Resistance, Neoplasm | |
dc.subject | Drug Screening Assays, Antitumor | |
dc.subject | Drug Synergism | |
dc.subject | Female | |
dc.subject | Gene Expression Regulation, Neoplastic | |
dc.subject | Gossypol | |
dc.subject | Humans | |
dc.subject | Imidazoles | |
dc.subject | Ovarian Neoplasms | |
dc.subject | RNA, Messenger | |
dc.subject | caspase 3 | |
dc.subject | caspase 7 | |
dc.subject | gossypol | |
dc.subject | messenger RNA | |
dc.subject | zoledronic acid | |
dc.subject | angiogenesis | |
dc.subject | apoptosis | |
dc.subject | article | |
dc.subject | cancer cell culture | |
dc.subject | cell death | |
dc.subject | cell proliferation | |
dc.subject | cell viability | |
dc.subject | controlled study | |
dc.subject | cytotoxicity | |
dc.subject | DNA fragmentation | |
dc.subject | down regulation | |
dc.subject | drug potentiation | |
dc.subject | enzyme activity | |
dc.subject | enzyme linked immunosorbent assay | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | IC 50 | |
dc.subject | ovary cancer | |
dc.title | Combined gossypol and zoledronic acid treatment results in synergistic induction of cell death and regulates angiogenic molecules in ovarian cancer cells | |
dc.type | Article |