Black P C
Department of Urologic Sciences, University of British Columbia, Vancouver, BC, USA.
Minerva Urol Nefrol. 2012 Mar;64(1):7-17.
Through our growing understanding of the molecular mechanisms that drive urothelial transformation and the growth, invasion and metastasis of bladder cancer, we are able to identify an increasingly broad spectrum of molecules and pathways that are suitable for novel targeted therapies. At the same time we are armed with an increasing number of agents designed to disrupt these signaling pathways, and, as these enter the clinical arena in other cancers, the barriers to use in bladder cancer patients decline. Targeted therapy for bladder cancer, however, remains in its infancy, and no major breakthroughs have been achieved. Here we review some of the molecular targets that have been best characterized in bladder cancer, as well as some of the newer targets that appear most promising. We will review the experience up to this point in testing targeted agents against these pathways, and describe some novel agents that have yet to be tested in clinical trials but have shown significant potential in pre-clinical models.
随着我们对驱动尿路上皮转化以及膀胱癌生长、侵袭和转移的分子机制的认识不断加深,我们能够识别出越来越多适合新型靶向治疗的分子和信号通路。与此同时,我们拥有越来越多旨在干扰这些信号通路的药物,并且,随着这些药物在其他癌症中进入临床应用,应用于膀胱癌患者的障碍也在减少。然而,膀胱癌的靶向治疗仍处于起步阶段,尚未取得重大突破。在此,我们综述一些在膀胱癌中已得到充分表征的分子靶点,以及一些看起来最有前景的新靶点。我们将回顾截至目前针对这些信号通路测试靶向药物的经验,并描述一些尚未在临床试验中进行测试但已在临床前模型中显示出巨大潜力的新型药物。