EZH2-Mediated Epigenetic Suppression of GDF15 Predicts a Poor Prognosis and Regulates Cell Proliferation in Non-Small-Cell Lung Cancer

被引:29
|
作者
Lu, Xiyi [1 ]
He, Xuezhi [2 ]
Su, Jun [3 ]
Wang, Jing [2 ]
Liu, Xinyin [1 ]
Xu, Kun [1 ]
De, Wei [4 ]
Zhang, Erbao [5 ]
Guo, Renhua [1 ]
Shi, Yuenian Eric [1 ]
机构
[1] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Res Ctr Bone & Stem Cells, Dept Anat Histol & Embryol, Nanjing 211166, Jiangsu, Peoples R China
[3] Southeast Univ, Affiliated Jiangyin Hosp, Dept Oncol, Med Coll, Jiangyin 214400, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Biochem & Mol Biol, Nanjing 211166, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat,Collaborat Innovat Ctr C, Jiangsu Key Lab Canc Biomarkers Prevent & Treatme, Nanjing 211166, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
TGF-BETA SUPERFAMILY; EXPRESSION; POLYCOMB; EZH2; MEMBER; CYCLOOXYGENASE; GDF-15/MIC-1; METHYLATION; STATISTICS; NAG-1;
D O I
10.1016/j.omtn.2018.05.016
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Growth differentiation factor 15 (GDF15), a member of the TGF-beta superfamily of cytokines, has been reported to exert very heterogeneous functions in various tumors. However, its expression and roles in mediating non-small-cell lung cancer (NSCLC) progression remain unknown. In this study, we found that GDF15 is downregulated in paired NSCLC tissues and correlated with poor clinical outcomes in NSCLC. A functional experiment demonstrated that overexpression of GDF15 significantly repressed NSCLC proliferation both in vitro and in vivo. Mechanistic studies reveal that inhibition of EZH2 expression prevented its binding to the GDF15 promoter region and reduced the trimethylation modification pattern of H3K27. Together, our data uncover that GDF15 is a direct target of EZH2 and, as a regulator of proliferation, might serve as a candidate prognostic biomarker and target for new therapies in human NSCLC.
引用
收藏
页码:309 / 318
页数:10
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