[The mTOR inhibitor enhances chemosensitivity of androgen-independent prostate cancer cell line]

Zhonghua Nan Ke Xue. 2009 Jul;15(7):617-20.
[Article in Chinese]

Abstract

Objective: To investigate the effect of the mammalian target of rapamycin (mTOR) inhibitor CCI-779 on the chemosensitivity of androgen-independent prostate cancer cell line PC-3.

Methods: Prostate cancer cells PC-3 were cultured and treated with CCI-779, Paclitaxel and combination of the two. Then the inhibitory effects of the three medications on the growth of the PC-3 cells were determined by MTT, and the their cell cycle and apoptosis were detected by flow cytometry.

Results: Compared with the control group, the three medications all significantly inhibited the proliferation of the PC-3 cells, and the combined method even enhanced the effect. Flow cytometry showed that CCI-779 and Paclitaxel blocked the cell cycle mainly in the G1/G2 stage, while the combined medication mainly in the G0/G1 stage. Significantly increased apoptosis of the PC-3 cells was observed in the three medication groups as compared with the control group (P < 0.01).

Conclusion: CCI-779 can inhibit the proliferation of PC-3 cells and enhance the chemosensitivity of prostate cancer.

Publication types

  • English Abstract

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Drug Therapy, Combination
  • Humans
  • Male
  • Paclitaxel / pharmacology
  • Prostatic Neoplasms / drug therapy
  • Protein Kinase Inhibitors / pharmacology*
  • Sirolimus / analogs & derivatives*
  • Sirolimus / antagonists & inhibitors*
  • Sirolimus / pharmacology

Substances

  • Antineoplastic Agents
  • Protein Kinase Inhibitors
  • temsirolimus
  • Paclitaxel
  • Sirolimus