Yun Eun-Jin, Lo U-Ging, Hsieh Jer-Tsong
Department of Urology, UT Southwestern Medical Center, Dallas, TX, USA.
Asian J Urol. 2016 Oct;3(4):203-210. doi: 10.1016/j.ajur.2016.09.006. Epub 2016 Sep 20.
Prostate cancer (PCa) is the most common cause of malignancy in males and the second leading cause of cancer mortality in United States. Current treatments for PCa include surgery, radiotherapy, and androgen-deprivation therapy. Eventually, PCa relapses to an advanced castration-resistant PCa (CRPC) that becomes a systematic disease and incurable. Therefore, identifying cellular components and molecular mechanisms that drive aggressive PCa at early stage is critical for disease prognosis and therapeutic intervention. One potential strategy for aggressive PCa is to target cancer stem cells (CSCs) that are identified by several unique characteristics such as immortal, self-renewal, and pluripotency. Also, CSC is believed to be a major factor contributing to resistance to radiotherapy and conventional chemotherapies. Moreover, CSCs are thought to be the critical cause of metastasis, tumor recurrence and cancer-related death of multiple cancer types, including PCa. In this review, we discuss recent progress made in understanding prostate cancer stem cells (PCSCs). We focus on the therapeutic strategies aimed at targeting specific surface markers of CSCs, the key signaling pathways in the maintenance of self-renewal capacity of CSCs, ATP-binding cassette (ABC) transporters that mediate the drug-resistance of CSCs, dysregulated microRNAs expression profiles in CSCs, and immunotherapeutic strategies developed against PCSCs surface markers.
前列腺癌(PCa)是男性最常见的恶性肿瘤病因,也是美国癌症死亡的第二大主要原因。目前针对PCa的治疗方法包括手术、放疗和雄激素剥夺疗法。最终,PCa会复发为晚期去势抵抗性前列腺癌(CRPC),成为一种全身性疾病且无法治愈。因此,识别在早期驱动侵袭性PCa的细胞成分和分子机制对于疾病预后和治疗干预至关重要。针对侵袭性PCa的一种潜在策略是靶向癌症干细胞(CSCs),这些细胞具有一些独特特征,如永生、自我更新和多能性。此外,CSC被认为是导致对放疗和传统化疗产生抗性的主要因素。而且,CSCs被认为是包括PCa在内的多种癌症类型发生转移、肿瘤复发和癌症相关死亡的关键原因。在本综述中,我们讨论了在理解前列腺癌干细胞(PCSCs)方面取得的最新进展。我们重点关注旨在靶向CSCs特定表面标志物的治疗策略、维持CSCs自我更新能力的关键信号通路、介导CSCs耐药性的ATP结合盒(ABC)转运蛋白、CSCs中失调的微小RNA表达谱以及针对PCSCs表面标志物开发的免疫治疗策略。