抗辐射性
鼻咽癌
PI3K/AKT/mTOR通路
蛋白激酶B
癌症研究
癌变
信号转导
抑制器
亮氨酸拉链
生物
化学
PTEN公司
放射治疗
磷酸化
医学
细胞生物学
内科学
生物化学
转录因子
基因
作者
Shuangbing Xu,Yan Li,Yutong Lu,Jing Huang,Jinghua Ren,Sheng Zhang,Zhongyuan Yin,Kai Huang,Gang Wu,Kunyu Yang
标识
DOI:10.1016/j.canlet.2018.01.067
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.
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