EIF5A2 is a novel chemoresistance gene in breast cancer

被引:30
|
作者
Liu, Yu [1 ]
Du, Feiya [1 ]
Chen, Wei [1 ]
Yao, Minya [1 ]
Lv, Kezhen [1 ]
Fu, Peifen [1 ]
机构
[1] Zhejiang Univ, Breast Ctr, Affiliated Hosp 1, Sch Med, Hangzhou 310003, Zhejiang, Peoples R China
关键词
eIF-5A2; Chemoresistance; Doxorubicin; Breast cancer; COMPARATIVE GENOMIC HYBRIDIZATION; INITIATION-FACTOR; 5A; EPITHELIAL-MESENCHYMAL TRANSITION; HYPUSINE-CONTAINING PROTEIN; CELL LUNG-CANCER; SACCHAROMYCES-CEREVISIAE; OVARIAN-CANCER; HEPATOCELLULAR-CARCINOMA; OVEREXPRESSION; EXPRESSION;
D O I
10.1007/s12282-014-0526-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The eIF5A2 gene (encoding the eukaryotic initiation factor 5A2) located at 3q26 is a putative oncogene that is overexpressed in colon and rectal carcinomas, lung cancer and hepatocellular carcinoma. EIF5A2 overexpression correlates significantly with tumor metastasis and is an adverse prognostic marker. However, eIF-5A2 overexpression in breast cancer and its effect on chemotherapy are unknown. Methods We measured eIF-5A2 expression and doxorubicin sensitivity in different human breast cancer cell lines (Bcap-1937, HCC1937, and MCF-7). To investigate a role for eIF-5A2 in chemoresistance, cells were treated with eIF-5A2-siRNA, exposed to various concentrations of doxorubicin, and toxicity was assayed by CCK-8 (cell counting kit). Results The eIF-5A2 expression levels varied among breast cancer cells. Higher expression levels correlated with decreased doxorubicin sensitivity. Silencing of eIF-5A2 significantly improved doxorubicin toxicity in all three breast cancer cell lines. Conclusion This study shows that eIF-5A2 plays an important role in doxorubicin chemoresistance in breast cancer cells.
引用
收藏
页码:602 / 607
页数:6
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