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CD133:超越癌症干细胞标志物。

CD133: beyond a cancer stem cell biomarker.

机构信息

a Department of Biochemistry, Faculty of Biotechnology and Biomolecular Science , Universiti Putra Malaysia , Serdang , Malaysia.

出版信息

J Drug Target. 2019 Mar;27(3):257-269. doi: 10.1080/1061186X.2018.1479756. Epub 2018 Jul 17.

Abstract

CD133 (prominin-1), a pentaspan membrane glycoprotein, is one of the most well-characterized biomarkers used for the isolation of cancer stem cells (CSCs). The presence of CSCs is one of the main causes of tumour reversal and resilience. Accumulating evidence has shown that CD133 might be responsible for CSCs tumourigenesis, metastasis and chemoresistance. It is now understood that CD133 interacts with the Wnt/β-catenin and PI3K-Akt signalling pathways. Moreover, CD133 can upregulate the expression of the FLICE-like inhibitory protein (FLIP) in CD133-positive cells, inhibiting apoptosis. In addition, CD133 can increase angiogenesis by activating the Wnt signalling pathway and increasing the expression of vascular endothelial growth factor-A (VEGF-A) and interleukin-8. Therefore, CD133 could be considered to be an 'Achilles' heel' for CSCs, because by inhibiting this protein, the signalling pathways that are involved in cell proliferation will also be inhibited. By understanding the molecular biology of CD133, we can not only isolate stem cells but can also utilise it as a therapeutic strategy. In this review, we summarise new insights into the fundamental cell biology of CD133 and discuss the involvement of CD133 in metastasis, metabolism, tumourigenesis, drug-resistance, apoptosis and autophagy.

摘要

CD133(prominin-1)是一种五跨膜糖蛋白,是用于分离癌症干细胞(CSC)的最著名的生物标志物之一。CSC 的存在是肿瘤逆转和耐药性的主要原因之一。越来越多的证据表明,CD133 可能负责 CSC 的肿瘤发生、转移和化疗耐药性。现在人们已经了解到,CD133 与 Wnt/β-catenin 和 PI3K-Akt 信号通路相互作用。此外,CD133 可以上调 CD133 阳性细胞中 FLICE 样抑制蛋白(FLIP)的表达,抑制细胞凋亡。此外,CD133 通过激活 Wnt 信号通路和增加血管内皮生长因子-A(VEGF-A)和白细胞介素-8 的表达来增加血管生成。因此,CD133 可以被认为是 CSC 的“阿喀琉斯之踵”,因为抑制这种蛋白质也会抑制参与细胞增殖的信号通路。通过了解 CD133 的分子生物学,我们不仅可以分离干细胞,还可以将其用作治疗策略。在这篇综述中,我们总结了 CD133 的基本细胞生物学的新见解,并讨论了 CD133 参与转移、代谢、肿瘤发生、耐药性、细胞凋亡和自噬的情况。

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