Bicyclic triterpenoid Iripallidal induces apoptosis and inhibits Akt/mTOR pathway in glioma cells
Autor: | Ellora Sen, Sadashib Ghosh, Vivek Sharma, Nitin Koul, Deobrat Dixit |
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Rok vydání: | 2010 |
Předmět: |
Cancer Research
Telomerase Blotting Western Apoptosis Biology lcsh:RC254-282 Cell Line Tumor Glioma Genetics medicine Humans Acrolein Protein kinase B PI3K/AKT/mTOR pathway Cell Proliferation Brain Neoplasms Caspase 3 Cell growth TOR Serine-Threonine Kinases Cell Cycle Cell cycle Cyclohexanols lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens medicine.disease Molecular biology Oncology Cancer research Signal transduction Glioblastoma Proto-Oncogene Proteins c-akt Research Article Signal Transduction |
Zdroj: | BMC Cancer, Vol 10, Iss 1, p 328 (2010) BMC Cancer |
ISSN: | 1471-2407 |
DOI: | 10.1186/1471-2407-10-328 |
Popis: | Background The highly resistant nature of glioblastoma multiforme (GBM) to chemotherapy prompted us to evaluate the efficacy of bicyclic triterpenoid Iripallidal against GBM in vitro. Methods The effect of Iripallidal on proliferation and apoptosis in glioma cell lines was evaluated by MTS, colony formation and caspase-3 activity. The effect of iripallidal to regulate (i) Akt/mTOR and STAT3 signaling (ii) molecules associated with cell cycle and DNA damage was evaluated by Western blot analysis. The effect of Iripallidal on telomerase activity was also determined. Results Iripallidal (i) induced apoptosis, (ii) inhibited Akt/mTOR and STAT3 signaling, (iii) altered molecules associated with cell cycle and DNA damage, (iv) inhibited telomerase activity and colony forming efficiency of glioma cells. In addition, Iripallidal displayed anti-proliferative activity against non-glioma cancer cell lines of diverse origin. Conclusion The ability of Iripallidal to serve as a dual-inhibitor of Akt/mTOR and STAT3 signaling warrants further investigation into its role as a therapeutic strategy against GBM. |
Databáze: | OpenAIRE |
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