4.7 Article

Sensitization to docetaxel in prostate cancer cells by green tea and quercetin

期刊

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 26, 期 4, 页码 408-415

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2014.11.017

关键词

Green tea polyphenol; Quercetin; Docetaxel; Prostate cancer; Combination

资金

  1. National Institutes of Health [NIH, NCI] [U54 CA143931-01, U54MD007598, UL1TR000124]
  2. NIH/National Center for Advancing Translational Sciences UCLA CTSI [KL2TR000122]
  3. National Institutes of Health [NIH, NIMHD] [U54 CA143931-01, U54MD007598, UL1TR000124]
  4. National Institutes of Health [NIH, NCATS] [U54 CA143931-01, U54MD007598, UL1TR000124]

向作者/读者索取更多资源

Chemotherapy with docetaxel (Doc) is a standard treatment for metastatic and castration-resistant prostate cancer. However, chemoresistance and side effects of Doc limit its clinical success. We investigated whether natural products green tea (GT) and quercetin (Q), a flavonoid from apples and onions, will enhance the efficacy of Doc in androgen-independent (Al) prostate cancer cells. Two cell lines including LAPC-4-Al and PC-3 were treated in vitro with 40 mu M of (-)-epigallocatechin gallate (EGCG), 5 mu M of Q 2 or 5 nM of Doc alone or in combination. The mixture of EGCG+Q+Doc increased the antiproliferative effect by threefold in LAPC-4-Al cells and eightfold in PC-3 cells compared to Doc alone. EGCG, Q and Doc in combination significantly enhanced cell cycle arrest at G2/M phase and increased apoptosis in both LAPC-4-Al and PC-3 cells compared to Doc alone. The mixture increased the inhibition of PI3/Akt and the signal transducer and activator of transcription (Stat) 3 signaling pathways compared to Doc alone, and decreased the protein expression of multidrug resistance-related protein. In addition, the combination with EGCG and Q increased the inhibition of tumor cell invasion and colony formation in both LAPC-4-Al and PC-3 cells compared to Doc alone, and decreased the percentage of CD44(+)/CD24(-) stem-like LAPC-4-AI cells. In summary, GT and Q enhanced the therapeutic effect of Doc in castration-resistant prostate cancer cells through multiple mechanisms including the down-regulation of chemoresistance-related proteins. This study provides a novel therapeutic modality to enhance the efficacy of Doc in a nontoxic manner. (C) 2015 Elsevier Inc. All rights reserved.

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