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INPP4B 介导的肿瘤耐药性与通过调节葡萄糖代谢相关,在喉癌细胞中通过调节己糖激酶 2 实现。

INPP4B-mediated tumor resistance is associated with modulation of glucose metabolism via hexokinase 2 regulation in laryngeal cancer cells.

机构信息

Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2013 Oct 11;440(1):137-42. doi: 10.1016/j.bbrc.2013.09.041. Epub 2013 Sep 17.

Abstract

Inositol polyphosphate 4-phosphatase type II (INPP4B) was recently identified as a tumor resistance factor in laryngeal cancer cells. Herein, we show that INPP4B-mediated resistance is associated with increased glycolytic phenotype. INPP4B expression was induced by hypoxia and irradiation. Intriguingly, overexpression of INPP4B enhanced aerobic glycolysis. Of the glycolysis-regulatory genes, hexokinase 2 (HK2) was mainly regulated by INPP4B and this regulation was mediated through the Akt-mTOR pathway. Notably, codepletion of INPP4B and HK2 markedly sensitized radioresistant laryngeal cancer cells to irradiation or anticancer drug. Moreover, INPP4B was significantly associated with HK2 in human laryngeal cancer tissues. Therefore, these results suggest that INPP4B modulates aerobic glycolysis via HK2 regulation in radioresistant laryngeal cancer cells.

摘要

肌醇多磷酸 4-磷酸酶 II 型(INPP4B)最近被鉴定为喉癌细胞中的肿瘤耐药因子。在此,我们表明 INPP4B 介导的耐药性与增加的糖酵解表型有关。缺氧和辐射诱导 INPP4B 的表达。有趣的是,INPP4B 的过表达增强了有氧糖酵解。在糖酵解调节基因中,己糖激酶 2(HK2)主要受 INPP4B 调节,这种调节是通过 Akt-mTOR 途径介导的。值得注意的是,INPP4B 和 HK2 的共缺失显著增强了对放疗或抗癌药物的耐药性喉癌细胞的敏感性。此外,INPP4B 在人喉癌组织中与 HK2 显著相关。因此,这些结果表明 INPP4B 通过调节 HK2 在耐辐射喉癌细胞中调节有氧糖酵解。

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