Identification of glycerol-3-phosphate dehydrogenase 1 as a tumour suppressor in human breast cancer

被引:31
作者
Zhou, Cefan [1 ,2 ]
Yu, Jing [2 ,3 ]
Wang, Ming [4 ]
Yang, Jing [5 ]
Xiong, Hui [6 ]
Huang, Huang [1 ]
Wu, Dongli [2 ]
Hu, Shimeng [2 ]
Wang, Yefu [2 ]
Chen, Xing-Zhen [1 ,7 ]
Tang, Jingfeng [1 ]
机构
[1] Hubei Univ Technol, Inst Biomed & Pharmaceut Sci, Key Lab Fermentat Engn,Hubei Key Lab Ind Microbio, Minist Educ,Hubei Prov Cooperat Innovat Ctr Ind F, Wuhan, Hubei, Peoples R China
[2] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan, Hubei, Peoples R China
[3] Hubei Canc Hosp, Dept Clin Lab, Wuhan, Hubei, Peoples R China
[4] Wuhan Univ, Dept Clin Lab, Renmin Hosp, Wuhan, Hubei, Peoples R China
[5] Tsinghua Univ, Inst Immunol, Beijing, Peoples R China
[6] XiLi Peoples Hosp, Shenzhen, Guangdong, Peoples R China
[7] Univ Alberta, Fac Med & Dent, Dept Physiol, Membrane Prot Dis Res Grp, Edmonton, AB, Canada
基金
中国国家自然科学基金;
关键词
prognostic significance; biomarker; cell proliferation; survival; meta-analysis; GENE-EXPRESSION; UP-REGULATION; MICRORNA-370; METABOLISM; OXIDATION; HALLMARK; LIVER; GPD1;
D O I
10.18632/oncotarget.21087
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the present study, we found the mRNA expression level of glycerol-3-phosphate dehydrogenase (GPD1) was significantly downregulated in human breast cancer patients. Patients with reduced GPD1 expression exhibited poorer overall metastatic relapse-free survival (p = 0.0013). Further Cox proportional hazard model analysis revealed that the reduced expression of GPD1 is an independent predictor of overall survival in oestrogen receptor-positive (p = 0.0027, HR = 0.91, 95% CI = 0.85-0.97, N = 3,917) and nodal-negative (p = 0.0013, HR = 0.87, 95% CI = 0.80-0.95, N = 2,456) breast cancer patients. We also demonstrated that GPD1 was a direct target of miR-370, which was significantly upregulated in human breast cancer. We further showed that exogenous expression of GPD1 in human MCF-7 and MDA-MB-231 breast cancer cells significantly inhibited cell proliferation, migration, and invasion. Our results, therefore, suggest a novel tumour suppressor function for GPD1 and contribute to the understanding of cancer metabolism.
引用
收藏
页码:101309 / 101324
页数:16
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