Mizutani Kosuke, Roca Hernan, Varsos Zachary, Pienta Kenneth J
Departments of Internal Medicine and Urology, University of Michigan School of Medicine, 7308 CCC 1500 E. Medical Center Drive, Ann Arbor, MI 48109-5946, USA.
Anticancer Res. 2009 Aug;29(8):3109-13.
C-C chemokine ligand 2 (CCL2) is a chemokine that has been demonstrated to play a pivotal role in prostate cancer tumorigenesis and metastasis. These effects are mediated by the ligand binding to the G protein-coupled receptor (GPCR) C-C chemokine receptor 2 (CCR2). It has recently been demonstrated that CCL2 increases Akt phosphorylation in prostate cancer cells, and prevents prostate cancer cells from autophagic death through activation of Akt pathway. The purpose of this study was to determine the mechanism by which CCL2 activates Akt in prostate cancer PC-3 cell line. CCL2-induced phosphorylation of Akt was inhibited by pertussis toxin and the adenylyl cyclase inhibitor SQ22536. Akt phosphorylation was promoted by prior treatment with cholera toxin. The results suggest that CCL2-induced Akt phosphorylation is mediated by the Galphai complex and adenylyl cyclase. This is the first study that demonstrates a direct involvement of adenylyl cyclase in CCL2-induced Akt phosphorylation.
C-C趋化因子配体2(CCL2)是一种趋化因子,已被证明在前列腺癌的肿瘤发生和转移中起关键作用。这些作用是由该配体与G蛋白偶联受体(GPCR)C-C趋化因子受体2(CCR2)结合介导的。最近有研究表明,CCL2可增加前列腺癌细胞中Akt的磷酸化,并通过激活Akt通路防止前列腺癌细胞自噬死亡。本研究的目的是确定CCL2在前列腺癌PC-3细胞系中激活Akt的机制。百日咳毒素和腺苷酸环化酶抑制剂SQ22536可抑制CCL2诱导的Akt磷酸化。用霍乱毒素预处理可促进Akt磷酸化。结果表明,CCL2诱导的Akt磷酸化是由Gαi复合体和腺苷酸环化酶介导的。这是第一项证明腺苷酸环化酶直接参与CCL2诱导的Akt磷酸化的研究。