标题:Growth factor progranulin promotes tumorigenesis of cervical cancer via PI3K/Akt/mTOR signaling pathway
作者:Feng, Tingting; Zheng, Lin; Liu, Feng; Xu, Xiaoying; Mao, Sheng; Wang, Xiao; Liu, Juan; Lu, Yi; Zhao, Weiming; Yu, Xiuping; Tang, 更多
作者机构:[Feng, Tingting; Zheng, Lin; Xu, Xiaoying; Mao, Sheng; Liu, Juan; Zhao, Weiming; Yu, Xiuping; Tang, Wei] Shandong Univ, Dept Pathogen Biol, Sch Med, J 更多
通讯作者:Tang, W
通讯作者地址:[Tang, W]Shandong Univ, Dept Pathogen Biol, Sch Med, Jinan, Shandong, Peoples R China.
来源:ONCOTARGET
出版年:2016
卷:7
期:36
页码:58381-58395
DOI:10.18632/oncotarget.11126
关键词:progranulin; mTOR signaling; tumorigenesis; transformation; cervical; cancer
摘要:Progranulin (PGRN) is an autocrine growth factor with tumorigenic roles in various tumors including cervical cancer. In this study, we investigated mammalian target of rapamycin (mTOR) signaling in response to PGRN induction and the contribution of the PGRN-stimulated PI3K/Akt/mTOR signaling pathway in the transformation and progression of cervical cancer. Here we identified a strong linkage between PGRN and phosphorylated-mTOR in cervical cancer tissues. PGRN promoted the phosphorylation of mTOR and activated mTOR signaling in human cervical mucosa epithelial cells and cervical cancer cells, and TNFR2 was needed for PGRN-stimulated mTOR signaling. Inhibition of mTOR signaling with rapamycin decreased PGRN-stimulated protein synthesis, transformation and proliferation of cervical cells in vitro, and tumor formation and growth in vivo. Thus, our findings update the signal transduction pathways of PGRN by suggesting that mTOR signaling contributes to PGRN-stimulated carcinogenesis of cervical cancer. Inhibition of PGRN/PI3K/Akt/mTOR signaling may be targeted in treatment of cervical cancer.
收录类别:SCIE
WOS核心被引频次:13
资源类型:期刊论文
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