Gallagher P E, Arter A L, Deng G, Tallant E A
Hypertension and Vascular Research Center, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1032, USA.
Curr Med Chem. 2014;21(21):2417-23. doi: 10.2174/0929867321666140205133357.
The development of peptides as therapeutic agents has progressed such that these small molecules of less than fifty amino acids are currently in use for the treatment of a variety of pathologies. This review focuses on the pre-clinical studies and clinical trials assessing the anti-cancer properties of angiotensin-(1-7) [Ang-(1-7)], an endogenous heptapeptide hormone of the renin-angiotensin system. Ang-(1-7) mediates biological responses by activating mas, a unique G protein- coupled receptor, thereby providing specific targeted actions when used as a therapeutic agent. Studies in in vitro as well as in vivo mouse models demonstrated that the heptapeptide hormone reduced proliferation of human cancer cells and xenograft tumors. This attenuation was concomitant with decreased angiogenesis, cancer associated fibrosis, osteoclastogenesis, tumor-induced inflammation and metastasis as well as altered regulation of growth promoting cellular signaling pathways. In three clinical trials, Ang-(1-7) was well tolerated with limited toxic or quality-of-life side effects and showed clinical benefit in cancer patients with solid tumors. Taken together, these studies suggest that Ang-(1-7) may serve as a first-in-class peptide chemotherapeutic agent, reducing cancer growth and metastases by pleiotrophic mechanisms as well as targeting the tumor microenvironment.
肽作为治疗药物的发展已经取得了进展,以至于这些由少于五十个氨基酸组成的小分子目前正被用于治疗多种病症。本综述重点关注评估肾素-血管紧张素系统的内源性七肽激素血管紧张素-(1-7) [Ang-(1-7)] 抗癌特性的临床前研究和临床试验。Ang-(1-7) 通过激活mas(一种独特的G蛋白偶联受体)介导生物学反应,因此在用作治疗药物时可提供特定的靶向作用。体外以及体内小鼠模型研究表明,这种七肽激素可减少人类癌细胞和异种移植肿瘤的增殖。这种抑制作用伴随着血管生成减少、癌症相关纤维化、破骨细胞生成、肿瘤诱导的炎症和转移减少,以及促进生长的细胞信号通路调节改变。在三项临床试验中,Ang-(1-7) 耐受性良好,毒性或生活质量方面的副作用有限,并在实体瘤癌症患者中显示出临床益处。综上所述,这些研究表明,Ang-(1-7) 可能作为一类首创的肽类化疗药物,通过多效机制以及靶向肿瘤微环境来减少癌症生长和转移。