Metformin inhibits prostate cancer cell proliferation, migration, and tumor growth through upregulation of PEDF expression

被引:55
作者
Chen, Xiaowan [1 ]
Li, Chenli [1 ]
He, Tiantian [1 ]
Mao, Jiating [1 ]
Li, Chunmei [1 ]
Lyu, Jianxin [1 ]
Meng, Qing H. [2 ]
机构
[1] Wenzhou Med Univ, Sch Lab Med & Life Sci, Zhejiang Prov Key Lab Med Genet, Key Lab Lab Med,Minist Educ China, Wenzhou, Zhejiang, Peoples R China
[2] Univ Texas MD Anderson Canc Ctr, Dept Lab Med, Houston, TX 77030 USA
基金
中国国家自然科学基金;
关键词
Antimetastatic; antitumorigenic; metformin; PEDF; proapoptotic; prostate cancer; tumor growth; EPITHELIUM-DERIVED FACTOR; ANTIDIABETIC DRUG METFORMIN; IN-VITRO; PIGMENT; DIFFERENTIATION; ACTIVATION; INCREASES; LIVER; RISK; AMPK;
D O I
10.1080/15384047.2016.1156273
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metformin has been reported to inhibit the growth of various types of cancers, including prostate cancer. Yet the mode of anti-cancer action of metformin and the underlying mechanisms remain not fully elucidated. We hypothesized that the antitumorigenic effects of metformin are mediated through upregulation of pigment epithelium-derived factor (PEDF) expression in prostate cancer cells. In this report, metformin treatment significantly inhibited the proliferation and colony formation of prostate cancer cells, in a dose-and time-dependent manner. Meanwhile, Metformin markedly suppressed migration and invasion and induced apoptosis of both LNCaP and PC3 cancer cells. Metformin also reduced PC3 tumor growth in BALB/c nude mice in vivo. Furthermore, metformin treatment was associated with higher PEDF expression in both prostate cancer cells and tumor tissue. Taken together, metformin inhibits prostate cancer cell proliferation, migration, invasion and tumor growth, and these activities are mediated by upregulation of PEDF expression. These findings provide a novel insight into the molecular functions of metformin as an anticancer agent.
引用
收藏
页码:507 / 514
页数:8
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