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Brefeldin A enhances docetaxel-induced growth inhibition and apoptosis in prostate cancer cells in monolayer and 3D cultures
Authors:Huarong Huang  Ting Liu  Junxi Guo  Lin Yu  Xiaofeng Wu  Yan He  Dongli Li  Junlei Liu  Kun Zhang  Xi Zheng  Susan Goodin
Institution:1. Allan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China;2. Department of Chemical Engineering and Environment, Wuyi University, Jiangmen 510060, China;3. Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States;4. Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, United States
Abstract:Docetaxel is a commonly used chemotherapeutic drug for patients with late stage prostate cancer. However, serious side effect and drug resistance limit its clinical success. Brefeldin A is a 16-membered macrolide antibiotic from mangrove-derived Fungus Aspergillus sp. (9Hu), which exhibited potent cytotoxicity against human cancer cells. In the present study, we determined the effect of brefeldin A on docetaxel-induced growth inhibition and apoptosis in human prostate cancer PC-3 cells. Brefeldin A in combination with docetaxel inhibited the growth of PC-3 cells in monolayer and in three dimensional cultures. The combination also potently stimulated apoptosis in PC-3 cells as determined by propidium iodide staining and morphological assessment. Mechanistic studies showed that growth inhibition and apoptosis in PC-3 cells treated with brefeldin A and docetaxel were associated with decrease in the level of Bcl-2. The present study indicates that combined brefeldin A with docetaxel may represent a novel approach for improving the efficacy of docetaxel, and Bcl-2 may serve as a target for brefeldin A to enhance the effects of docetaxel chemotherapy.
Keywords:Brefeldin A  Docetaxel  Prostate cancer  Bcl-2  3D culture
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