Herrmann Edwin, Bögemann Martin, Bierer Stefan, Eltze Elke, Hertle Lothar, Wülfing Christian
Department of Urology, University of Münster, Albert-Schweitzer Strasse 33, 48149 Münster, Germany.
Expert Rev Anticancer Ther. 2006 Jan;6(1):73-81. doi: 10.1586/14737140.6.1.73.
Endothelin (ET)-1 and its receptors ET-A and ET-B, referred to commonly as the endothelin axis, have been identified in various human cancers, especially gynecologic tumors, such as breast cancer or ovarian cancer, but also including urologic tumor entities. They play a key role in tumor growth and progression by influencing critical cancer pathways, such as apoptosis, angiogenesis and proliferation. In prostate cancer, overexpression of the ET-A receptor increases with tumor progression, and clinical trials with selective ET-A receptor antagonists, such as atrasentan (ABT-627), have shown promising early results. In preclinical models of bladder cancer, overexpression of the ET axis has been demonstrated and ET-targeting agents are under investigation. This paper reviews the role of the ET axis in human cancers and focuses on preclinical and clinical studies in urologic tumor entities to further define the role of ET-targeting agents as targeted molecular therapy.
内皮素(ET)-1及其受体ET-A和ET-B,通常被称为内皮素轴,已在多种人类癌症中被发现,尤其是妇科肿瘤,如乳腺癌或卵巢癌,也包括泌尿系统肿瘤实体。它们通过影响关键的癌症途径,如细胞凋亡、血管生成和增殖,在肿瘤生长和进展中发挥关键作用。在前列腺癌中,ET-A受体的过度表达随肿瘤进展而增加,使用选择性ET-A受体拮抗剂(如阿曲生坦(ABT-627))的临床试验已显示出有希望的早期结果。在膀胱癌的临床前模型中,已证实内皮素轴过度表达,并且针对内皮素的药物正在研究中。本文综述了内皮素轴在人类癌症中的作用,并重点关注泌尿系统肿瘤实体的临床前和临床研究,以进一步确定针对内皮素的药物作为靶向分子疗法的作用。