Overcoming chemoresistance in prostate cancer with Chinese medicine Tripterygium wilfordii via multiple mechanisms

被引:22
|
作者
Wang, Zhijun [1 ]
Ravula, Ranadheer [2 ]
Shi, Leming [3 ,4 ,5 ]
Song, Yunjie [3 ,4 ,5 ]
Yeung, Steven [1 ]
Liu, Mandy [2 ]
Lau, Bernard [1 ]
Hao, Jijun [6 ]
Wang, Jeffrey [2 ]
Lam, Christopher Wai Kei [7 ]
Chow, Moses Sing Sum [1 ]
Huang, Ying [2 ]
机构
[1] Western Univ Hlth Sci, Coll Pharm, Ctr Adv Drug Res & Evaluat, Pomona, CA 91766 USA
[2] Western Univ Hlth Sci, Coll Pharm, Dept Pharmaceut Sci, Pomona, CA 91766 USA
[3] Fudan Univ, State Key Lab Genet Engn, Ctr Pharmacogen, Shanghai, Peoples R China
[4] Fudan Univ, Sch Life Sci, MOE Key Lab Contemporary Anthropol, Shanghai, Peoples R China
[5] Fudan Univ, Sch Pharm, Shanghai, Peoples R China
[6] Western Univ Hlth Sci, Coll Vet, Pomona, CA USA
[7] Macau Univ Sci & Technol, Macau Inst Appl Res Med & Hlth, State Key Lab Qual Res Chinese Med, Taipa, Macau, Peoples R China
关键词
chemotherapy; resistance; Chinese medicine; tripterygium wilfordii; prostate cancer; DOCETAXEL RESISTANCE; HEME OXYGENASE-1; CELL-MIGRATION; EXPRESSION; INHIBITION; ANTICANCER; CELASTROL; GROWTH; LINES;
D O I
10.18632/oncotarget.10868
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A leading cause of cancer chemotherapy failure is chemoresistance, which often involves multiple mechanisms. Chinese medicines (CM) usually contain multiple components which could potentially target many mechanisms simultaneously and may offer an advantage over single compounds that target one mechanism at a time. The purpose of this study was to investigate the chemosensitizing effect (CE) of a specific CM, tripterygium wilfordii (TW), on prostate cancer cells resistant to docetaxel (Dtx) and identify the potential mechanisms. The CE of TW (in combination with Dtx) was evaluated in two Dtx resistant prostate cancer cell lines (PC3-TxR and DU145-TxR) and the efficacy of the combination for resistant PC3-TxR tumor was investigated using a xenograft mouse model. For mechanistic study, the inhibitory effect of TW on P-glycoprotein activity was assessed. In addition, novel gene targets of TW were identified using DNA microarray and quantitative PCR. Results showed that TW induced a CE of 8 and >38 folds in PC3-TxR and DU145-TxR cells, respectively with Dtx IC50 reversed back to that of the sensitive parent cells. An optimum dose of TW+Dtx significantly retarded tumor growth in mice compared to TW or Dtx alone. TW inhibited P-glycoprotein activity and induced a significant gene expression changes in genes related to angiogenesis, cell cycle regulation and differentiation. Our in vitro and in vivo studies demonstrate that TW in combination with Dtx was able to overcome the chemoresistance and suppress resistant prostate tumor growth via multi-mechanisms.
引用
收藏
页码:61246 / 61261
页数:16
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