Rybak Adrian P, Bristow Robert G, Kapoor Anil
McMaster Institute of Urology, Division of Urology, Department of Surgery, McMaster University, ON, Canada.
St. Joseph's Hospital, Hamilton, ON, Canada.
Oncotarget. 2015 Feb 10;6(4):1900-19. doi: 10.18632/oncotarget.2953.
The cells of the prostate gland are dependent on cell signaling pathways to regulate their growth, maintenance and function. However, perturbations in key signaling pathways, resulting in neoplastic transformation of cells in the prostate epithelium, are likely to generate subtypes of prostate cancer which may subsequently require different treatment regimes. Accumulating evidence supports multiple sources of stem cells in the prostate epithelium with distinct cellular origins for prostate tumorigenesis documented in animal models, while human prostate cancer stem-like cells (PCSCs) are typically enriched by cell culture, surface marker expression and functional activity assays. As future therapies will require a deeper understanding of its cellular origins as well as the pathways that drive PCSC maintenance and tumorigenesis, we review the molecular and functional evidence supporting dysregulation of PI3K/AKT, RAS/MAPK and STAT3 signaling in PCSCs, the development of castration resistance, and as a novel treatment approach for individual men with prostate cancer.
前列腺细胞依赖细胞信号通路来调节其生长、维持和功能。然而,关键信号通路的扰动会导致前列腺上皮细胞发生肿瘤转化,进而可能产生前列腺癌的不同亚型,随后可能需要不同的治疗方案。越来越多的证据支持前列腺上皮中存在多种干细胞来源,动物模型已证明前列腺肿瘤发生具有不同的细胞起源,而人前列腺癌干细胞样细胞(PCSC)通常通过细胞培养、表面标志物表达和功能活性测定来富集。由于未来的治疗需要更深入地了解其细胞起源以及驱动PCSC维持和肿瘤发生的信号通路,我们综述了支持PCSC中PI3K/AKT、RAS/MAPK和STAT3信号失调、去势抵抗发展以及作为前列腺癌个体新治疗方法的分子和功能证据。