Transcriptional activation of ANO1 promotes gastric cancer progression

被引:22
|
作者
Zeng, Xiaoqing [1 ]
Pan, Duyi [1 ]
Wu, Hao [2 ]
Chen, Hao [3 ]
Yuan, Wei [4 ]
Zhou, Ji [1 ]
Shen, Zhenbin [3 ]
Chen, Shiyao [1 ,5 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Gastroenterol & Hepatol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Key Lab Glycoconjugate Res Minist Publ Hlth, Shanghai 200032, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Gen Surg, Shanghai 200032, Peoples R China
[4] Fudan Univ, Zhongshan Hosp, Dept Pathol, Shanghai 200032, Peoples R China
[5] Fudan Univ, Zhongshan Hosp, Endoscopy Ctr, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
ANO1; SP1; MLL1; Gastric cancer; Progression; TUMOR-GROWTH; EXPRESSION; CONTRIBUTES; CARCINOMA;
D O I
10.1016/j.bbrc.2019.03.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prognosis of gastric cancer (GC) remains poor due to local invasion and distal metastasis. The GC related molecular mechanisms underlying invasion and metastasis are not well understood. In this study, we investigated the functional role of ANO1 in GC progression. We found that ANO1 is overexpressed in GC tissues and correlated with GC tumor-node-metastasis stage. Knockdown of ANO1 significantly inhibited GC cell migration and invasion in vitro, and loss of ANO1 resulted in inhibition of tumor metastasis in vivo. Mechanistically, SP1 increased ANO1 transcription, recruited MLL1 to the ANO1 promoter region, facilitated H3K4 trimethylation, and subsequently promoted ANO1 expression. Together, our findings provide a mechanistic assessment of ANO1 overexpression, which represents a GC progression-related molecule and a potentially valuable target for future research. (C) 2019 The Authors. Published by Elsevier Inc.
引用
收藏
页码:131 / 136
页数:6
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