MicroRNA-7: A critical sensitizer for TRAIL sensitivity in glioblastoma cells

Xiao Zhang, A. Yang, Rui Zhang
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引用次数: 1

Abstract

TRAIL (TNF-related apoptosis-inducing ligand) is a promising anticancer agent because of its tumor-specifc apoptosis inducer activity without affecting normal cells. MicroRNAs (miRNAs) emerge as important regulators of cell viability. Our recent studies showed that miR-7 is a potential sensitizer for TRAIL-induced apoptosis in glioblastoma (GBM) cells, and XIAP is a critical gene in the apoptotic process as a direct downstream gene of miR-7. Additionally, this regulatory axis could also exert in other types of tumor cells. More importantly, we confirmed that co-delivery of sTRAIL and tumor suppressor miR-7 by MSCs leads to synergistic cancer killing effect. Thus, miR-7 has been demonstrated to be a critical sensitizer for TRAIL-induced apoptosis through regulating XIAP and highlights a novel therapeutic strategy for the treatment of GBM.
MicroRNA-7:胶质母细胞瘤细胞TRAIL敏感性的关键增敏剂
TRAIL(TNF相关的凋亡诱导配体)是一种很有前途的抗癌剂,因为它具有肿瘤特异性的凋亡诱导活性,而不影响正常细胞。微小RNA(miRNA)是细胞活力的重要调节因子。我们最近的研究表明,miR-7是TRAIL诱导的胶质母细胞瘤(GBM)细胞凋亡的潜在敏化剂,XIAP作为miR-7的直接下游基因是凋亡过程中的关键基因。此外,这种调节轴也可以在其他类型的肿瘤细胞中发挥作用。更重要的是,我们证实了间充质干细胞共同递送sTRAIL和肿瘤抑制因子miR-7会产生协同的癌症杀伤作用。因此,miR-7已被证明是TRAIL通过调节XIAP诱导的细胞凋亡的关键敏化剂,并突出了治疗GBM的新治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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