Alvarez-Cubero Maria J, Vázquez-Alonso Fernando, Puche-Sanz Ignacio, Ortega F Gabriel, Martin-Prieto M, Garcia-Puche José L, Pascual-Geler Manrique, Lorente José A, Cozar-Olmo José M, Serrano Maria J
GENYO, Centre for Genomics and Oncological Research, Pfizer / University of Granada / Andalusian Regional Government, PTS Granada Av. de la Ilustración, 114 - 18016, GRANADA, Spain.
Curr Drug Targets. 2016;17(6):693-701. doi: 10.2174/1389450116666150309121346.
Circulating Tumor Cells (CTCs) are a valuable prognostic factor in several solid tumors. By understanding the biological characteristics of CTCs we could better understand the biology of metastasis. CTCs usually adopt a dormant state that is believed to be a strategy to survive in extreme conditions. To enter a dormant state, CTCs undergo numerous phenotypic, genetic and functional mutations that significantly affect the efficacy of the therapies used to kill dormant CTCs. Hence, understanding the biological events involved in the dormancy process of CTCs would allow the identification of new therapeutic targets. Some experimental studies or preclinical models have explored these biological events, as well as the molecular factors that contribute to the maintenance of and release from dormancy. However, few studies have assessed the effects of anticancer therapies on dormant cells. This study reviews current the data currently available on cell dormancy mechanisms in prostate cancer, with a special focus on the functional, genetic and phenotypic plasticity of CTCs and their potential implications in the clinical and therapeutic management of prostate cancer.
循环肿瘤细胞(CTCs)是几种实体瘤中一种有价值的预后因素。通过了解CTCs的生物学特性,我们可以更好地理解转移生物学。CTCs通常处于休眠状态,这被认为是在极端条件下生存的一种策略。为了进入休眠状态,CTCs会经历大量表型、基因和功能突变,这显著影响用于杀死休眠CTCs的疗法的疗效。因此,了解CTCs休眠过程中涉及的生物学事件将有助于识别新的治疗靶点。一些实验研究或临床前模型已经探索了这些生物学事件,以及有助于维持休眠和从休眠中释放的分子因素。然而,很少有研究评估抗癌疗法对休眠细胞的影响。本研究回顾了目前关于前列腺癌细胞休眠机制的现有数据,特别关注CTCs的功能、基因和表型可塑性及其在前列腺癌临床和治疗管理中的潜在意义。