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癌症干细胞及其微环境中的CXCL12交叉点

The CXCL12 Crossroads in Cancer Stem Cells and Their Niche.

作者信息

López-Gil Juan Carlos, Martin-Hijano Laura, Hermann Patrick C, Sainz Bruno

机构信息

Department of Cancer Biology, Instituto de Investigaciones Biomédicas "Alberto Sols" (IIBM), CSIC-UAM, 28029 Madrid, Spain.

Department of Biochemistry, Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.

出版信息

Cancers (Basel). 2021 Jan 26;13(3):469. doi: 10.3390/cancers13030469.

Abstract

Cancer stem cells (CSCs) are defined as a subpopulation of "stem"-like cells within the tumor with unique characteristics that allow them to maintain tumor growth, escape standard anti-tumor therapies and drive subsequent repopulation of the tumor. This is the result of their intrinsic "stem"-like features and the strong driving influence of the CSC niche, a subcompartment within the tumor microenvironment that includes a diverse group of cells focused on maintaining and supporting the CSC. CXCL12 is a chemokine that plays a crucial role in hematopoietic stem cell support and has been extensively reported to be involved in several cancer-related processes. In this review, we will provide the latest evidence about the interactions between CSC niche-derived CXCL12 and its receptors-CXCR4 and CXCR7-present on CSC populations across different tumor entities. The interactions facilitated by CXCL12/CXCR4/CXCR7 axes seem to be strongly linked to CSC "stem"-like features, tumor progression, and metastasis promotion. Altogether, this suggests a role for CXCL12 and its receptors in the maintenance of CSCs and the components of their niche. Moreover, we will also provide an update of the therapeutic options being currently tested to disrupt the CXCL12 axes in order to target, directly or indirectly, the CSC subpopulation.

摘要

癌症干细胞(CSCs)被定义为肿瘤内具有独特特征的“干细胞”样细胞亚群,这些特征使其能够维持肿瘤生长、逃避标准抗肿瘤治疗并驱动肿瘤的后续再增殖。这是其内在“干细胞”样特征以及癌症干细胞生态位强大驱动影响的结果,癌症干细胞生态位是肿瘤微环境中的一个亚区室,包括一组致力于维持和支持癌症干细胞的不同细胞群。CXCL12是一种趋化因子,在造血干细胞支持中起关键作用,并且已有大量报道表明其参与多种癌症相关过程。在本综述中,我们将提供关于癌症干细胞生态位衍生的CXCL12与其在不同肿瘤实体的癌症干细胞群体上存在的受体CXCR4和CXCR7之间相互作用的最新证据。由CXCL12/CXCR4/CXCR7轴介导的相互作用似乎与癌症干细胞的“干细胞”样特征、肿瘤进展和转移促进密切相关。总之,这表明CXCL12及其受体在维持癌症干细胞及其生态位组成部分中发挥作用。此外,我们还将提供目前正在测试的旨在破坏CXCL12轴以直接或间接靶向癌症干细胞亚群的治疗选择的最新情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b6/7866198/4111c983fad5/cancers-13-00469-g001.jpg

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