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通过基因工程嵌合抗原受体T细胞靶向癌症干细胞

Targeting Cancer Stem Cells by Genetically Engineered Chimeric Antigen Receptor T Cells.

作者信息

Alhabbab Rowa Y

机构信息

Division of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Front Genet. 2020 Apr 22;11:312. doi: 10.3389/fgene.2020.00312. eCollection 2020.

Abstract

The term cancer stem cell (CSC) starts 25 years ago with the evidence that CSC is a subpopulation of tumor cells that have renewal ability and can differentiate into several distinct linages. Therefore, CSCs play crucial role in the initiation and the maintenance of cancer. Moreover, it has been proposed throughout several studies that CSCs are behind the failure of the conventional chemo-/radiotherapy as well as cancer recurrence due to their ability to resist the therapy and their ability to re-regenerate. Thus, the need for targeted therapy to eliminate CSCs is crucial; for that reason, chimeric antigen receptor (CAR) T cells has currently been in use with high rate of success in leukemia and, to some degree, in patients with solid tumors. This review outlines the most common CSC populations and their common markers, in particular CD133, CD90, EpCAM, CD44, ALDH, and EGFR, the interaction between CSCs and the immune system, CAR T cell genetic engineering and signaling, CAR T cells in targeting CSCs, and the barriers in using CAR T cells as immunotherapy to treat solid cancers.

摘要

癌症干细胞(CSC)这一术语始于25年前,当时有证据表明CSC是肿瘤细胞的一个亚群,具有自我更新能力,并且能够分化为几种不同的细胞谱系。因此,CSC在癌症的起始和维持过程中起着至关重要的作用。此外,多项研究表明,由于CSC具有抵抗治疗的能力和重新再生的能力,传统的化学/放射治疗失败以及癌症复发都与CSC有关。因此,采用靶向治疗来消除CSC至关重要;出于这个原因,嵌合抗原受体(CAR)T细胞目前已成功应用于白血病治疗,在一定程度上也应用于实体瘤患者。这篇综述概述了最常见的CSC群体及其常见标志物,特别是CD133、CD90、上皮细胞黏附分子(EpCAM)、CD44、乙醛脱氢酶(ALDH)和表皮生长因子受体(EGFR),CSC与免疫系统之间的相互作用,CAR T细胞的基因工程和信号传导,CAR T细胞靶向CSC的情况,以及将CAR T细胞用作免疫疗法治疗实体癌的障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e5/7188929/224c6394680d/fgene-11-00312-g001.jpg

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