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雄激素受体作为晚期前列腺癌治疗耐药的驱动因素。

Androgen receptor as a driver of therapeutic resistance in advanced prostate cancer.

作者信息

Kahn Barbara, Collazo Joanne, Kyprianou Natasha

机构信息

Departments of Urology and Molecular and Cellular Biochemistry, University of Kentucky, College of Medicine, Lexington, KY 40536, USA.

出版信息

Int J Biol Sci. 2014 Jun 1;10(6):588-95. doi: 10.7150/ijbs.8671. eCollection 2014.

Abstract

The role of the androgen receptor (AR) signaling axis in the progression of prostate cancer is a cornerstone to our understanding of the molecular mechanisms causing castration-resistant prostate cancer (CRPC). Resistance of advanced prostate cancer to available treatment options makes it a clinical challenge that results in approximately 30,000 deaths of American men every year. Since the historic discovery by Dr. Huggins more than 70 years ago, androgen deprivation therapy (ADT) has been the principal treatment for advanced prostate cancer. Initially, ADT induces apoptosis of androgen-dependent prostate cancer epithelial cells and regression of androgen-dependent tumors. However, the majority of patients with advanced prostate cancer progress and become refractory to ADT due to emergence of androgen-independent prostate cancer cells driven by aberrant AR activation. Microtubule-targeting agents such as taxanes, docetaxel and paclitaxel, have enjoyed success in the treatment of metastatic prostate cancer; although new, recently designed mitosis-specific agents, such as the polo-kinase and kinesin-inhibitors, have yielded clinically disappointing results. Docetaxel, as a first-line chemotherapy, improves prostate cancer patient survival by months, but tumor resistance to these therapeutic agents inevitably develops. On a molecular level, progression to CRPC is characterized by aberrant AR expression, de novo intraprostatic androgen production, and cross talk with other oncogenic pathways. Emerging evidence suggests that reactivation of epithelial-mesenchymal-transition (EMT) processes may facilitate the development of not only prostate cancer but also prostate cancer metastases. EMT is characterized by gain of mesenchymal characteristics and invasiveness accompanied by loss of cell polarity, with an increasing number of studies focusing on the direct involvement of androgen-AR signaling axis in EMT, tumor progression, and therapeutic resistance. In this article, we discuss the current knowledge of mechanisms via which the AR signaling drives therapeutic resistance in prostate cancer metastatic progression and the novel therapeutic interventions targeting AR in CRPC.

摘要

雄激素受体(AR)信号轴在前列腺癌进展中的作用是我们理解导致去势抵抗性前列腺癌(CRPC)分子机制的基石。晚期前列腺癌对现有治疗方案产生耐药性,这使其成为一项临床挑战,每年导致约30000名美国男性死亡。自70多年前哈金斯博士的历史性发现以来,雄激素剥夺疗法(ADT)一直是晚期前列腺癌的主要治疗方法。最初,ADT诱导雄激素依赖性前列腺癌上皮细胞凋亡以及雄激素依赖性肿瘤消退。然而,大多数晚期前列腺癌患者会进展并对ADT产生耐药,这是由于异常AR激活驱动的雄激素非依赖性前列腺癌细胞的出现。紫杉烷类、多西他赛和紫杉醇等微管靶向药物在转移性前列腺癌治疗中取得了成功;尽管新设计的、针对有丝分裂的新型药物,如波罗蛋白激酶和驱动蛋白抑制剂,临床效果令人失望。多西他赛作为一线化疗药物,可使前列腺癌患者生存期延长数月,但肿瘤对这些治疗药物的耐药性不可避免地会出现。在分子水平上,向CRPC进展的特征是AR异常表达、前列腺内雄激素的重新产生以及与其他致癌途径的相互作用。新出现的证据表明,上皮-间质转化(EMT)过程的重新激活不仅可能促进前列腺癌的发展,还可能促进前列腺癌转移。EMT的特征是获得间质特性和侵袭性,同时伴有细胞极性丧失,越来越多的研究关注雄激素-AR信号轴在EMT、肿瘤进展和治疗耐药中的直接作用。在本文中,我们讨论了AR信号驱动前列腺癌转移进展中治疗耐药的机制的现有知识,以及针对CRPC中AR的新型治疗干预措施。

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