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首页> 外文期刊>Pathology oncology research: POR >Expression and Clinical Significance of Translation Regulatory Long Non-Coding RNA 1 ( TRERNA1 ) in Ependymomas
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Expression and Clinical Significance of Translation Regulatory Long Non-Coding RNA 1 ( TRERNA1 ) in Ependymomas

机译:翻译调节性长期非编码RNA 1(TRERNA1)在ENENCYMAS中的表达及临床意义

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Long noncoding RNAs (lncRNA) have emerged as vital molecules governing epithelial-to-mesenchymal transition (EMT) in cancers. Translation regulatory RNA 1 (TRERNA1) is one such lncRNA known to enhance the transcriptional activity of the EMT-transcription factor, Snail. We have previously demonstrated differential upregulation of EMT-transcription factors and cadherin switching across various clinico-pathologic-molecular subclasses of ependymomas (EPN). With an aim to analyze the correlation between the expression of TRERNA1 in EPNs, we performed gene expression analysis for TRERNA1 on 75 Grade II/III EPNs and correlated with tumor site, C11orf95-RELA fusions, age, MIB-1 proliferative indices, and outcome wherever available. Upregulation of gene expression levels of TRERNA1 was seen in intracranial EPNs, with highest expression levels in pediatric posterior fossa EPNs. High TRERNA1 expression was found associated with higher proliferative indices (p = 0.034) and shorter progression free survival (p = 0.002). Our study, for the first time, demonstrates an association between TRERNA1 expressions and pediatric posterior fossa EPNs. Further in-vivo and in-vitro studies are required to confirm these findings and evaluate TRERNA1 as a novel biomarker and potential therapeutic target in childhood PF-EPNs.
机译:长度非编码RNA(LNCRNA)被出现为治疗癌症上皮 - 间充质转换(EMT)的重要分子。翻译调节RNA 1(TRERNA1)是一种已知的一种这样的LNCRNA,用于增强EMT转录因子蜗牛的转录活性。我们之前已经表现出对EMT-转录因子和钙粘蛋白切换的差异上调,跨越Enencomomas(EPN)的各种临床病理分子亚类。目的是分析EPNS中Trerna1表达与EPNS的表达之间的相关性,我们对75级II / III EPN进行TRERNA1的基因表达分析,与肿瘤部位,C11ORF95-RELA融合,年龄,MIB-1增殖指数和结果相关联无论何处可用。在颅内EPNS中观察到TRERNA1的基因表达水平的上调,具有足够的表达水平在儿科后浮肿EPN。发现高TRERNA1表达与较高的增殖指数相关(P = 0.034)和较短的进展自由存活(p = 0.002)。我们的研究首次展示了Trerna1表达和儿科后窝epns之间的关联。需要进一步的体内和体外研究来确认这些发现,并评估Trerna1作为新的生物标志物和儿童PF-EPN中的潜在治疗靶标。

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