Yeung Man Lung, Yasunaga Jun-ichirou, Bennasser Yamina, Dusetti Nelson, Harris David, Ahmad Nafees, Matsuoka Masao, Jeang Kuan-Teh
Molecular Virology Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.
Cancer Res. 2008 Nov 1;68(21):8976-85. doi: 10.1158/0008-5472.CAN-08-0769.
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 11 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.
微小RNA(miRNA)在人类T细胞白血病病毒1型(HTLV-1)介导的细胞转化中的作用尚未见报道。在此,我们分析了HTLV-1转化的人类T细胞系以及成体T细胞白血病患者外周血单个核细胞中的miRNA表达。对11种不同图谱的分析揭示了6种持续上调的miRNA。其中两种上调的miRNA(miR-93和miR-130b)靶向一种肿瘤抑制蛋白——肿瘤蛋白53诱导核蛋白1(TP53INP1)的mRNA的3'非翻译区(3'UTR)。在HTLV-1转化的细胞中发现TP53INP1蛋白的表达水平较低。此外,当使用抗miR来敲低这些细胞中的miR-93和miR-130b时,TP53INP1的表达增加,这表明前者在细胞内对后者具有调控作用。通过实验证实增强TP53INP1表达会增加细胞凋亡,从而确立了TP53INP1在调节细胞生长中的作用。总体而言,这些发现表明存在一个影响HTLV-1感染/转化细胞增殖和存活的miR-93/miR-130b-TP53INP1轴。