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
相关论文
共 49 条
[31]  
Mori N, 1996, CANCER RES, V56, P779
[32]   AN INDUCIBLE TRANSCRIPTION FACTOR ACTIVATES EXPRESSION OF HUMAN-IMMUNODEFICIENCY-VIRUS IN T-CELLS [J].
NABEL, G ;
BALTIMORE, D .
NATURE, 1987, 326 (6114) :711-713
[33]   Microarray-based, high-throughput gene expression profiling of microRNAs [J].
Nelson, PT ;
Baldwin, DA ;
Scearce, LM ;
Oberholtzer, JC ;
Tobias, JW ;
Mourelatos, Z .
NATURE METHODS, 2004, 1 (02) :155-161
[34]   c-Myc-regulated microRNAs modulate E2F1 expression [J].
O'Donnell, KA ;
Wentzel, EA ;
Zeller, KI ;
Dang, CV ;
Mendell, JT .
NATURE, 2005, 435 (7043) :839-843
[35]   p53DINP1, a p53-inducible gene, regulates p53-dependent apoptosis [J].
Okamura, S ;
Arakawa, H ;
Tanaka, T ;
Nakanishi, H ;
Ng, CC ;
Taya, Y ;
Monden, M ;
Nakamura, Y .
MOLECULAR CELL, 2001, 8 (01) :85-94
[36]   THE HUMAN LYMPHOTROPIC-T VIRUS TYPE-I TAX GENE CAN COOPERATE WITH THE RAS ONCOGENE TO INDUCE NEOPLASTIC TRANSFORMATION OF CELLS [J].
POZZATTI, R ;
VOGEL, J ;
JAY, G .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (01) :413-417
[37]   Abnormal microRNA-16 locus with synteny to human 13q14 linked to CLL in NZB mice [J].
Raveche, Elizabeth S. ;
Salerno, Erica ;
Scaglione, Brian J. ;
Manohar, Vijaya ;
Abbasi, Fatima ;
Lin, Yi-Chu ;
Fredrickson, Torgny ;
Landgraf, Pablo ;
Ramachandra, Sumant ;
Huppi, Konrad ;
Toro, Jorge R. ;
Zenger, Vincent E. ;
Metcalf, Robert A. ;
Marti, Gerald E. .
BLOOD, 2007, 109 (12) :5079-5086
[38]   MCM7 amplification and overexpression are associated with prostate cancer progression [J].
Ren, B ;
Yu, G ;
Tseng, GC ;
Cieply, K ;
Gavel, T ;
Michalopoulos, G ;
Yu, YP ;
Luo, JH .
ONCOGENE, 2006, 25 (07) :1090-1098
[39]   microRNAs in viral oncogenesis [J].
Scaria, Vinod ;
Jadhav, Vaibhav .
RETROVIROLOGY, 2007, 4
[40]   MicroRNA 29c is down-regulated in nasopharyngeal carcinomas, up-regulating mRNAs encoding extracellular matrix proteins [J].
Sengupta, Srikumar ;
den Boon, Johan A. ;
Chen, I-How ;
Newton, Michael A. ;
Stanhope, Stephen A. ;
Cheng, Yu-Juen ;
Chen, Chien-Jen ;
Hildesheim, Allan ;
Sugden, Bill ;
Ahlquist, Paul .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (15) :5874-5878