Profiling MicroRNA expression in hepatocellular carcinoma reveals MicroRNA-224 up-regulation and apoptosis inhibitor-5 as a MicroRNA-224-specific target

被引:307
作者
Wang, Yu [2 ]
Lee, Alvin T. C. [1 ]
Ma, Joel Z. I. [2 ]
Wang, Jingbo [2 ]
Ren, Jianwei [1 ]
Yang, Yuchen [3 ]
Tantoso, Erwin [3 ]
Li, Kuo-Bin [3 ]
Ooi, London L. P. J. [1 ,4 ]
Tan, Patrick [5 ]
Lee, Caroline G. L. [1 ,2 ,5 ]
机构
[1] Natl Canc Ctr, Div Med Sci, Dept Surg Oncol, Singapore 169610, Singapore
[2] Natl Univ Singapore, Dept Biochem, Singapore 119077, Singapore
[3] Bioinformat Inst, Singapore 138671, Singapore
[4] Singapore Gen Hosp, Dept Surg, Singapore 169608, Singapore
[5] Duke NUS Grad Med Sch, Singapore 169547, Singapore
关键词
D O I
10.1074/jbc.M707629200
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
Like other cancers, aberrant gene regulation features significantly in hepatocellular carcinoma (HCC). MicroRNAs (miRNAs) were recently found to regulate gene expression at the post-transcriptional/ translational levels. The expression profiles of 157 miRNAs were examined in 19 HCC patients, and 19 up-regulated and 3 down-regulated miRNAs were found to be associated with HCC. Putative gene targets of these 22 miRNAs were predicted in silico and were significantly enriched in 34 biological pathways, most of which are frequently dysregulated during carcinogenesis. Further characterization of microRNA-224 (miR-224), the most significantly upregulated miRNA in HCC patients, revealed that miR-224 increases apoptotic cell death as well as proliferation and targets apoptosis inhibitor-5 (API-5) to inhibit API-5 transcript expression. Significantly, miR-224 expression was found to be inversely correlated with API-5 expression in HCC patients (p < 0.05). Hence, our findings define a true in vivo target of miR-224 and reaffirm the important role of miRNAs in the dysregulation of cellular processes that may ultimately lead to tumorigenesis.
引用
收藏
页码:13205 / 13215
页数:11
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