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癌症干细胞:前景与潜力

Cancer stem cells: the promise and the potential.

作者信息

Ajani Jaffer A, Song Shumei, Hochster Howard S, Steinberg Ira B

机构信息

Professor, Department of Gastrointestinal (GI) Medical Oncology, Division of Cancer Medicine; Professor, Department of Epidemiology, Division of OVP, Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX.

Associate Professor, Department of Gastrointestinal (GI) Medical Oncology-Research, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

出版信息

Semin Oncol. 2015 Apr;42 Suppl 1:S3-17. doi: 10.1053/j.seminoncol.2015.01.001. Epub 2015 Jan 21.

Abstract

Despite the advancement of treatment modalities, many cancer patients experience tumor recurrence and metastasis at regional or distant sites. Evolving understanding of tumor biology has led to the hypothesis that tumors may possess a stem cell-like subpopulation known as cancer stem cells (CSCs) that may be involved in driving tumor propagation and pathogenesis. Like normal stem cells (NSCs), CSCs can be identified by markers such as CD133, CD44, and ALDH. CSCs have the ability to self-renew and differentiate into different tumor components through stemness pathways, such as Wnt, TGF-β, STAT, and Hippo-YAP/TAZ, among others. In NSCs, stemness pathways are strictly regulated and control many important biologic processes, including embryogenesis and intestinal crypt cellular regulation. In contrast, stemness pathways in CSCs are significantly dysregulated. Combining current drugs with the targeting of these stemness pathways may significantly improve patient prognosis. The aim of this supplement is to update clinicians on the accumulated evidence characterizing the role of CSCs in tumor initiation, heterogeneity, therapy resistance, and recurrence and metastasis, and the potential for effectively treating patients.

摘要

尽管治疗方式不断进步,但许多癌症患者仍会在局部或远处发生肿瘤复发和转移。对肿瘤生物学的深入理解催生了一种假说,即肿瘤可能拥有一种类似干细胞的亚群,称为癌症干细胞(CSCs),它们可能参与驱动肿瘤的增殖和发病机制。与正常干细胞(NSCs)一样,CSCs可通过CD133、CD44和醛脱氢酶(ALDH)等标志物来识别。CSCs具有自我更新的能力,并可通过干性途径(如Wnt、转化生长因子-β(TGF-β)、信号转导和转录激活因子(STAT)以及Hippo-YAP/TAZ等)分化为不同的肿瘤成分。在NSCs中,干性途径受到严格调控,并控制着许多重要的生物学过程,包括胚胎发育和肠道隐窝细胞调节。相比之下,CSCs中的干性途径则明显失调。将目前的药物与针对这些干性途径的治疗相结合,可能会显著改善患者的预后。本增刊的目的是向临床医生介绍有关CSCs在肿瘤起始、异质性、治疗抵抗、复发和转移中的作用的累积证据,以及有效治疗患者的潜力。

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