DU145型
LNCaP公司
PI3K/AKT/mTOR通路
蛋白激酶B
前列腺癌
癌症研究
癌细胞
癌症
体内
细胞凋亡
细胞生长
细胞周期
活力测定
齐墩果酸
化学
医学
生物
内科学
病理
生物化学
替代医学
生物技术
作者
Xuechao Li,Yarong Song,Peng Zhang,Hongxue Zhu,Haiyong Chen,Yajun Xiao,Yifei Xing
出处
期刊:Tumor Biology
[SAGE Publishing]
日期:2015-12-18
卷期号:37 (6): 7599-7613
被引量:59
标识
DOI:10.1007/s13277-015-4655-9
摘要
Oleanolic acid (OA) is a naturally occurring pentacyclic triterpenoid and possesses diverse pharmacological activities, including anti-cancer effects that have been confirmed in multiple types of human cancers. However, the potential effect of natural OA on human prostate cancer is still unclear. The present study aimed to explore whether and how OA exerted anti-cancer effects in prostate cancer. Our data showed that OA inhibited cell viability and proliferation, and promoted cell apoptosis and G0/G1 phase cell cycle arrest in prostate cancer PC-3, DU145, and LNCaP cells, in a dose-dependent manner. In addition, OA was found to regulate the expression levels of apoptosis-related and cell cycle-related proteins, as well as the activity of PI3K/Akt pathway, in a dose-dependent manner. Mechanistically, our data revealed that OA exerted anti-cancer effects in vitro in PC-3 and DU145 cells by repressing the PI3K/Akt pathway. In agreement, OA also suppressed the tumor growth of PC-3 cells in vivo via inhibition of the PI3K/Akt pathway. In conclusion, our findings demonstrate the anti-cancer properties of OA in prostate cancer cells, both in vitro and in vivo, and provide the experimental evidence for the use of OA as an adjuvant agent for prostate cancer patients.
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