Molecular Pathology Laboratory 'A', Regina Elena National Cancer Institute, Rome, Italy.
Br J Pharmacol. 2011 May;163(2):220-33. doi: 10.1111/j.1476-5381.2011.01217.x.
The endothelins (ET) are a group of proteins that act through G-protein coupled receptors. Endothelin-1 (ET-1) was initially identified as a potent vasoconstrictor and dysregulation of the ET axis contributes to pathological processes responsible for cardiovascular disease states. More recently, the ET axis, in particular ET-1 acting through the endothelin A receptor (ET(A) ), has been implicated in the development of several cancers through activation of pathways involved in cell proliferation, migration, invasion, epithelial-mesenchymal transition, osteogenesis and angiogenesis. The endothelin B receptor (ET(B) ) may counter tumour progression by promoting apoptosis and clearing ET-1; however, it has recently been implicated in the development of some tumour types including melanomas and oligodendrogliomas. Here, we review emerging preclinical and clinical data outlining the role of the ET axis in cancer, and its antagonism as an attractive and challenging approach to improve clinical cancer management. Clinical data of ET(A) antagonists in patients with prostate cancer are encouraging and provide promise for new ET(A) antagonist-based treatment strategies. Given the unexpected opportunities to affect pleiotrophic tumorigenic signals by targeting ET(A)-mediated pathways in a number of cancers, the evaluation of ET-targeted therapy in cancer warrants further investigation.
内皮素(ET)是一组通过 G 蛋白偶联受体起作用的蛋白质。内皮素-1(ET-1)最初被鉴定为一种强效血管收缩剂,ET 轴的失调导致心血管疾病状态的病理过程。最近,ET 轴,特别是通过内皮素 A 受体(ET(A))发挥作用的 ET-1,已被牵连到几种癌症的发展中,通过激活涉及细胞增殖、迁移、侵袭、上皮-间充质转化、成骨和血管生成的途径。内皮素 B 受体(ET(B))可能通过促进细胞凋亡和清除 ET-1 来对抗肿瘤进展;然而,它最近被牵连到一些肿瘤类型的发展中,包括黑色素瘤和少突胶质细胞瘤。在这里,我们综述了概述 ET 轴在癌症中的作用及其作为改善临床癌症管理的有吸引力和具有挑战性的方法的新兴临床前和临床数据。ET(A)拮抗剂在前列腺癌患者中的临床数据令人鼓舞,并为新的基于 ET(A)拮抗剂的治疗策略提供了希望。鉴于通过靶向多种癌症中 ET(A)介导的途径来影响多效性肿瘤发生信号的意外机会,ET 靶向治疗在癌症中的评估值得进一步研究。