miR-342-3p suppresses cell proliferation and migration by targeting AGR2 in non-small cell lung cancer

被引:81
|
作者
Xue, Xiaofeng [1 ]
Fei, Xiaoyan [2 ]
Hou, Wenjie [1 ]
Zhang, Yajie [2 ]
Liu, Liu [3 ]
Hu, Rongkuan [2 ,4 ,5 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Suzhou 215006, Jiangsu, Peoples R China
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Biochem, 5390 Harry Hines, Dallas, TX 75390 USA
[3] An Hui Med Univ, Anhui Prov Hosp, Dept Gen Surg, Hefei, Anhui, Peoples R China
[4] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei, Anhui, Peoples R China
[5] Univ Sci & Technol China, Sch Life Sci, Hefei, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
AGR2; miR-342-3p; Non-small cell lung cancer; Cell proliferation; Cell migration; GROWTH-FACTOR RECEPTOR; METASTASIS MARKER AGR2; HIGH EXPRESSION; PROMOTES; INVASION; MUTATIONS; PHENOTYPE; PATHWAY; ANTIGEN; GENE;
D O I
10.1016/j.canlet.2017.10.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
AGR2 is a well-studied secreted protein that is involved in multiple biological processes including cell proliferation and migration. The mechanism by which AGR2 increases the growth and migration of non small cell lung cancer cells (NSCLC) is still unknown. In this study, we report that AGR2 is directly targeted by miR-342-3p. Functional studies suggest that overexpression of miR-342-3p inhibits the proliferation and migration of non-small cell lung cancer cells. Overexpression of AGR2 counteracts the phenotypes induced by miR-342-3p. Moreover, AGR2 expression is up-regulated and negatively correlated with miR-342-3p levels in NSCLC cells and tissues. A meta-analysis of survival data indicates that NSCLC patients with high levels of AGR2 in their tumors have a worse prognosis. Collectively, the identification of miR-342-3p and AGR2 might facilitate the development of biomarkers and therapeutic targets for this devastating disease. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:170 / 178
页数:9
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