Bagnato Anna, Rosanò Laura
Molecular Pathology and Ultrastructure, Regina Elena Cancer Institute, Via delle Messi d'Oro 156, 00158 Rome, Italy.
Int J Biochem Cell Biol. 2008;40(8):1443-51. doi: 10.1016/j.biocel.2008.01.022. Epub 2008 Feb 1.
The endothelin axis, comprising endothelins and their receptors, has recently emerged as relevant player in tumor growth and metastasis by regulating mitogenesis, cell survival, angiogenesis, bone remodeling, stimulation of nociceptor receptor, tumor-infiltrating immune cells, epithelial-to-mesenchymal transition, invasion and metastatic dissemination. Endothelin-1 participates in the growth and progression of a variety of tumors such as prostatic, ovarian, renal, pulmonary, colorectal, cervical, breast, bladder, endometrial carcinomas, Kaposi's sarcoma, brain tumors, melanoma, and bone metastases. This review highlights key signaling pathways activated by endothelin-1 axis in cancer, since the understanding the full spectrum activated by endothelin-1 is critical for the optimal design of targeted therapies. Preliminary experimental and clinical data demonstrate that interfering with endothelin receptor by using endothelin-1 receptor antagonists alone and in combination with cytotoxic drugs or molecular inhibitors could represent a new mechanism-based antitumor strategy.
内皮素轴由内皮素及其受体组成,最近已成为肿瘤生长和转移的相关参与者,它通过调节有丝分裂、细胞存活、血管生成、骨重塑、刺激伤害感受器受体、肿瘤浸润免疫细胞、上皮-间质转化、侵袭和转移扩散发挥作用。内皮素-1参与多种肿瘤的生长和进展,如前列腺癌、卵巢癌、肾癌、肺癌、结直肠癌、宫颈癌、乳腺癌、膀胱癌、子宫内膜癌、卡波西肉瘤、脑肿瘤、黑色素瘤和骨转移瘤。本综述强调了内皮素-1轴在癌症中激活的关键信号通路,因为了解内皮素-1激活的全谱对于靶向治疗的优化设计至关重要。初步的实验和临床数据表明,单独使用内皮素-1受体拮抗剂以及与细胞毒性药物或分子抑制剂联合使用来干扰内皮素受体,可能代表一种基于新机制的抗肿瘤策略。