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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >MicroRNA-146a Downregulates NF{kappa}B Activity via Targeting TRAF6 and Functions as a Tumor Suppressor Having Strong Prognostic Implications in NK/T Cell Lymphoma.
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MicroRNA-146a Downregulates NF{kappa}B Activity via Targeting TRAF6 and Functions as a Tumor Suppressor Having Strong Prognostic Implications in NK/T Cell Lymphoma.

机译:MicroRNA-146a通过靶向TRAF6下调NF {kappa} B的活性,并充当在NK / T细胞淋巴瘤中具有强烈预后意义的肿瘤抑制因子。

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PURPOSE: We investigated prognostic implications of microRNAs in extranodal NK/T cell lymphoma (NKTL). EXPERIMENTAL DESIGN: We measured miRNA expression in NKTL tissues and cell lines, using real-time PCR, and analyzed its role in NKTL, using cell lines. RESULTS: Multivariate analysis showed low miR-146a expression (P < 0.001; HR = 13.110), primary non-upper aerodigestive tract lesion (non-UAT; P = 0.008; HR = 5.376) and high International Prognostic Index (IPI; >/=3; P = 0.013; HR = 3.584) to be independent poor prognostic factors. miR-146a expression could subdivide UAT-NKTL into 2 prognostic groups, resulting in the following prognostic groups: (i) UAT(Low-146a), (ii) UAT(High-146a), and (iii) non-UAT. Compared with UAT(High-146a), UAT(Low-146a) showed distinctively poor prognosis (P < 0.001; HR = 15.620), similar to the non-UAT group. In vitro, miR-146a overexpression in NKTL cell lines, SNK6 and YT, inhibited nuclear factor kappaB (NFkappaB) activity, suppressed cell proliferation, induced apoptosis, and enhanced chemosensitivity. TNF receptor-associated factor 6, a target of miR-146a and a known NFkappaB activator, was downregulated by miR-146a in SNK6 and YT cells. Promoter methylation of miR-146a gene was observed in SNK6 and YT cells, as well as in NKTL tissues with low miR-146a expression, and miR-146a expression was induced by the conversion of methylation status with a demethylating agent in SNK6 and YT cells. CONCLUSIONS: These results suggest that miR-146a might function as a potent tumor suppressor in NKTL and be useful for patient assessment and therapeutic targeting. Clin Cancer Res; 17(14); 4761-71. (c)2011 AACR.
机译:目的:我们调查了结外NK / T细胞淋巴瘤(NKTL)中microRNA的预后意义。实验设计:我们使用实时PCR测量了NKTL组织和细胞系中miRNA的表达,并使用细胞系分析了其在NKTL中的作用。结果:多变量分析显示miR-146a表达低(P <0.001; HR = 13.110),原发性非上消化道病变(非UAT; P = 0.008; HR = 5.376)和高国际预后指数(IPI;> / = 3; P = 0.013; HR = 3.584)是独立的不良预后因素。 miR-146a表达可将UAT-NKTL细分为2个预后组,从而导致以下预后组:(i)UAT(Low-146a),(ii)UAT(High-146a)和(iii)非UAT。与UAT(High-146a)相比,UAT(Low-146a)的预后明显较差(P <0.001; HR = 15.620),与非UAT组相似。在体外,miR-146a在NKTL细胞系SNK6和YT中的过表达抑制核因子kappaB(NFkappaB)活性,抑制细胞增殖,诱导细胞凋亡,并增强化学敏感性。 TNF受体相关因子6(miR-146a的靶标和已知的NFkappaB激活剂)在SNK6和YT细胞中被miR-146a下调。在SNK6和YT细胞以及低miR-146a表达的NKTL组织中观察到miR-146a基因的启动子甲基化,并且通过脱甲基剂在SNK6和YT细胞中甲基化状态的转换诱导miR-146a表达。 。结论:这些结果表明,miR-146a可能在NKTL中起有效的抑癌作用,可用于患者评估和治疗靶向。临床癌症研究; 17(14); 4761-71。 (c)2011年美国机修协会。

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