Schatton Tobias, Frank Natasha Y, Frank Markus H
Transplantation Research Center, Children's Hospital Boston & Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Bioessays. 2009 Oct;31(10):1038-49. doi: 10.1002/bies.200900058.
Cancer stem cells (CSC) represent malignant cell subsets in hierarchically organized tumors, which are selectively capable of tumor initiation and self-renewal and give rise to bulk populations of non-tumorigenic cancer cell progeny through differentiation. Robust evidence for the existence of prospectively identifiable CSC among cancer bulk populations has been generated using marker-specific genetic lineage tracking of molecularly defined cancer subpopulations in competitive tumor development models. Moreover, novel mechanisms and relationships have been discovered that link CSC to cancer therapeutic resistance and clinical tumor progression. Importantly, proof-of-principle for the potential therapeutic utility of the CSC concept has recently been provided by demonstrating that selective killing of CSC through a prospective molecular marker can inhibit tumor growth. Herein, we review these novel and translationally relevant research developments and discuss potential strategies for CSC-targeted therapy in the context of resistance mechanisms and molecular pathways preferentially operative in CSC.
癌症干细胞(CSC)是分层组织肿瘤中的恶性细胞亚群,它们具有选择性的肿瘤起始和自我更新能力,并通过分化产生大量非致瘤性癌细胞后代。利用竞争性肿瘤发展模型中分子定义的癌症亚群的标记特异性遗传谱系追踪,已获得大量证据证明在癌症总体人群中存在可前瞻性识别的癌症干细胞。此外,还发现了将癌症干细胞与癌症治疗抗性和临床肿瘤进展联系起来的新机制和关系。重要的是,最近通过证明通过前瞻性分子标记选择性杀死癌症干细胞可以抑制肿瘤生长,为癌症干细胞概念的潜在治疗效用提供了原理证明。在此,我们回顾这些新颖且与转化相关的研究进展,并在癌症干细胞中优先起作用的抗性机制和分子途径的背景下讨论针对癌症干细胞治疗的潜在策略。