Roles for MicroRNAs, miR-93 and miR-130b, and Tumor Protein 53-induced Nuclear Protein 1 Tumor Suppressor in Cell Growth Dysregulation by Human T-Cell Lymphotrophic Virus 1

被引:148
作者
Yeung, Man Lung [1 ]
Yasunaga, Jun-ichirou [1 ,2 ]
Bennasser, Yamina [1 ,4 ]
Dusetti, Nelson [3 ]
Harris, David [5 ]
Ahmad, Nafees [5 ]
Matsuoka, Masao [2 ]
Jeang, Kuan-Teh [1 ]
机构
[1] NIAID, Mol Virol Sect, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[2] Kyoto Univ, Inst Virus Res, Lab Virus Immunol, Sakyo Ku, Kyoto 606, Japan
[3] Univ Mediterrance, INSERM, IFR 137, Inst Cancerol & Immunol Marseille,U624, Marseille, France
[4] CNRS, Mol Virol Lab, Inst Genet Humaine, UPR 1142, Montpellier, France
[5] Univ Arizona, Dept Microbiol & Immunol, Hlth Sci Ctr, Tucson, AZ 85721 USA
关键词
D O I
10.1158/0008-5472.CAN-08-0769
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A role for microRNAs (miRNA) in human T-cell leukemia virus 1 (HTLV-1)-mediated cellular transformation has not been described. Here, we profiled miRNA expression in HTLV-1-transformed human T-cell lines and primary peripheral blood mononuclear cells from adult T-cell leukemia patients. Analyses of I I different profiles revealed six miRNAs that were consistently up-regulated. Two of the up-regulated miRNAs (miR-93 and miR-130b) target the 3' untranslated region (3'UTR) of the mRNA for a tumor suppressor protein, tumor protein 53-induced nuclear protein 1 (TP53INP1). A low expression level of TP53INP1 protein was found in HTLV-1-transformed cells. Additionally, when antagomirs were used to knock down miR-93 and miR-130b in these cells, the expression of TP53INP1 was increased, suggesting that the latter is regulated inside cells by the former. A role for TP53INP1 in regulating cell growth was established by experiments that showed that enhanced TP53INP1 expression increased apoptosis. Collectively, the findings implicate a miR-93/miR-130b-TP53INP1 axis that affects the proliferation and survival of HTLV-1-infected/transformed cells. [Cancer Res 2008;68(21):8976-85]
引用
收藏
页码:8976 / 8985
页数:10
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