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微小RNA-223/配对盒基因6轴通过调控磷脂酰肌醇-3-激酶/蛋白激酶B信号通路调节胶质母细胞瘤干细胞增殖及对替莫唑胺的化疗耐药性。

MiR-223/PAX6 Axis Regulates Glioblastoma Stem Cell Proliferation and the Chemo Resistance to TMZ via Regulating PI3K/Akt Pathway.

作者信息

Huang Bai-Sheng, Luo Qi-Zhi, Han Yang, Huang Dong, Tang Qing-Ping, Wu Li-Xiang

机构信息

Department of Physiology, School of Basic Medical Science, Central South University, Changsha 410008, P. R. China.

Department of Immunology, School of Basic Medical Science, Central South University, Changsha 410008, P. R. China.

出版信息

J Cell Biochem. 2017 Oct;118(10):3452-3461. doi: 10.1002/jcb.26003. Epub 2017 Jun 6.

DOI:10.1002/jcb.26003
PMID:28332226
Abstract

Chemotherapy is a standard strategy for glioma, while chemoresistance remains a major therapeutic challenge in current clinical practice. Our present study was aimed to determine whether inhibition of the miR-223/paired box 6 (PAX6) pathway could increase the sensitivity of glioma to Temozolomide. An elevated level of miR-223 was observed in glioma tissues. Exogenous miR-223 promoted cell survival when exposed to Temozolomide (TMZ), while miR-223 inhibition could reverse this process. The RNA and protein levels of PAX6 were significantly decreased by exogenous miR-223, and the 3'-untranslated region of PAX6 was shown to be a target of miR-223. Besides, it has also been reported that PI3K/Akt signaling pathway is pivotal to regulate glioma growth and proliferation. In the present study, we revealed that miR-223/PAX6 axis regulated the growth, invasion, and chemo resistance of glioblastoma stem cells to TMZ via regulating PI3K/Akt signaling pathway, which present a novel potential therapy for intervention of glioblastoma. Taken together, our findings shed new light on the miR-223/PAX6 pathway in glioma and this pathway might modulate the sensitivity of glioma to TMZ via regulating PI3K/Akt signaling pathway. J. Cell. Biochem. 118: 3452-3461, 2017. © 2017 Wiley Periodicals, Inc.

摘要

化疗是胶质瘤的标准治疗策略,然而在当前临床实践中,化疗耐药仍然是一个主要的治疗挑战。我们目前的研究旨在确定抑制miR-223/配对盒6(PAX6)通路是否能增加胶质瘤对替莫唑胺的敏感性。在胶质瘤组织中观察到miR-223水平升高。外源性miR-223在暴露于替莫唑胺(TMZ)时促进细胞存活,而抑制miR-223可逆转这一过程。外源性miR-223使PAX6的RNA和蛋白质水平显著降低,并且PAX6的3'-非翻译区被证明是miR-223的一个靶点。此外,也有报道称PI3K/Akt信号通路对调节胶质瘤的生长和增殖至关重要。在本研究中,我们揭示miR-223/PAX6轴通过调节PI3K/Akt信号通路来调控胶质母细胞瘤干细胞对TMZ的生长、侵袭和化疗耐药性,这为胶质母细胞瘤的干预提供了一种新的潜在治疗方法。综上所述,我们的研究结果为胶质瘤中的miR-223/PAX6通路提供了新的见解,并且该通路可能通过调节PI3K/Akt信号通路来调节胶质瘤对TMZ的敏感性。《细胞生物化学杂志》118: 3452 - 3461, 2017。© 2017威利期刊公司

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