Department of Urology Yokohama City University Graduate School of Medicine, 3-9, Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan.
Curr Cancer Drug Targets. 2011 May;11(4):442-50. doi: 10.2174/156800911795538101.
Angiotensin II (Ang-II) plays a role not only as a vasoconstrictor in controlling blood pressure and electrolyte and fluid homeostasis, but also as a mitogenic factor through the Ang-II type-1 (AT1) receptor in cardiovascular cells. Since a low prevalence of cancer in hypertensive patients receiving angiotensin converting enzyme inhibitors has been reported, the molecular mechanisms of the renin-angiotensin system (RAS) in cancer cells have been elucidated. Interestingly, there is increasing evidence that the RAS is implicated in the development of prostate cancer. As previously reported, AT1 receptor blockers (ARBs), a class of antihypertensive agent, have the potential to inhibit the growth of prostate cancer cells and tumors through the AT1 receptor. This review highlights that the RAS plays a potential role in various aspects of prostate cancer, and ARBs could be useful for treatment of prostate cancer or its chemoprevention.
血管紧张素 II(Ang-II)不仅作为血管收缩剂在控制血压、电解质和体液平衡中发挥作用,而且还通过心血管细胞中的血管紧张素 II 型 1(AT1)受体作为有丝分裂原因子发挥作用。由于报告称接受血管紧张素转换酶抑制剂的高血压患者癌症的患病率较低,因此已经阐明了癌细胞中肾素-血管紧张素系统(RAS)的分子机制。有趣的是,越来越多的证据表明 RAS 与前列腺癌的发展有关。如前所述,血管紧张素 II 受体阻滞剂(ARB)作为一类降压药,通过 AT1 受体具有抑制前列腺癌细胞和肿瘤生长的潜力。这篇综述强调了 RAS 在前列腺癌的各个方面都发挥了潜在作用,ARB 可能有助于治疗前列腺癌或其化学预防。