LZTS2 inhibits PI3K/AKT activation and radioresistance in nasopharyngeal carcinoma by interacting with p85

被引:48
作者
Xu, Shuangbing [1 ]
Li, Yan [1 ]
Lu, Yanwei [1 ]
Huang, Jing [1 ]
Ren, Jinghua [1 ]
Zhang, Sheng [1 ]
Yin, Zhongyuan [1 ]
Huang, Kai [2 ]
Wu, Gang [1 ]
Yang, Kunyu [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Canc Ctr, Wuhan 430022, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Clin Ctr Human Gene Res, Wuhan 430022, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
LZT52; p85; PI3K; Radioresistance; Nasopharyngeal carcinoma; ZIPPER TUMOR-SUPPRESSOR; BETA-CATENIN; SIGNALING PATHWAY; CANCER-CELLS; PROTEIN; DIFFERENTIATION; PROLIFERATION; TRANSCRIPTION; EXPRESSION; CHALLENGES;
D O I
10.1016/j.canlet.2018.01.067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phosphoinositide 3-kinase (PI3K) activity is aberrantly activated in nasopharyngeal carcinoma. However, the underlying mechanisms remain unclear. Here, we found that Leucine zipper tumor suppressor 2 (LZTS2) was downregulated and predicted poor prognosis in nasopharyngeal carcinoma patients. Furthermore, we identified the PI3K subunit p85 as a novel LZTS2-interacting protein using an unbiased proteomics approach. Moreover, we demonstrated that LZTS2 competes with p110 for p85 binding and inhibits activation of the PI3K/AKT signaling pathway. Functionally, we showed that LZTS2 suppresses tumorigenesis and radioresistance in nasopharyngeal carcinoma in a p85-dependent manner. Taken together, our results not only provide understanding of the molecular mechanisms by which PI3K/AKT signaling is activated but also suggest that targeting the LZTS2/PI3K/AKT signaling axis is a promising therapeutic strategy for radiosensitization of nasopharyngeal carcinoma. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 48
页数:11
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