Università di Palermo, Section of Medical Oncology, Department of Surgical and Oncological Sciences, Via del Vespro 129, 90127 Palermo, Italy.
Expert Opin Emerg Drugs. 2010 Mar;15(1):27-40. doi: 10.1517/14728210903571667.
The endothelin (ET) axis, which includes the biological functions of ETs and their receptors, has played a physiological role in normal tissue, acting as a modulator of vasomotor tone, tissue differentiation and development, cell proliferation and hormone production. Interestingly, it also functions in the growth and progression of various tumors. Several researchers have identified the blockade of the ET-1 receptor as a promising therapeutic approach.
The clinical investigation of an orally bioavailable ET antagonist, atrasentan, in prostate cancer, is encouraging. In this neoplasia, it has shown antitumor activity, bone metastasis control and amelioration of cancer-related pain but improvement in time to progression and overall survival has still not been demonstrated. The clinical trials of other ET antagonists are reported. Literature research was performed by Pubmed and Pharmaprojects.
A comprehensive view about the use of atrasentan in the treatment of castration-resistant prostate cancer (CRPC) is provided together with the scientific rationale based on the function of ET and its receptor in various cancer development mechanisms.
Atrasentan seems to be active in CRPC, although strong scientific evidence is still to be found. Interesting clinical findings regard zibotentan.
内皮素 (ET) 轴,包括 ETs 和其受体的生物学功能,在正常组织中发挥了生理作用,作为血管舒缩张力、组织分化和发育、细胞增殖和激素产生的调节剂。有趣的是,它在各种肿瘤的生长和进展中也发挥作用。一些研究人员已经确定了阻断 ET-1 受体是一种很有前途的治疗方法。
在前列腺癌中,临床研究一种口服生物可利用的 ET 拮抗剂阿曲生坦是令人鼓舞的。在这种肿瘤中,它显示出抗肿瘤活性、骨转移控制和改善癌症相关疼痛,但仍未证明进展时间和总生存期的改善。报道了其他 ET 拮抗剂的临床试验。文献研究通过 Pubmed 和 Pharmaprojects 进行。
提供了关于阿曲生坦在治疗去势抵抗性前列腺癌 (CRPC) 中的应用的全面观点,并基于 ET 及其受体在各种癌症发展机制中的功能提供了科学依据。
尽管仍需要强有力的科学证据,但阿曲生坦似乎对 CRPC 有效。关于齐泊坦的有趣临床发现。