Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, 110029, India.
Pathol Oncol Res. 2020 Jul;26(3):1975-1981. doi: 10.1007/s12253-019-00736-8. Epub 2019 Sep 5.
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.
长链非编码 RNA(lncRNA)已成为调控癌症上皮间质转化(EMT)的重要分子。TRERNA1 是一种已知的 lncRNA,可增强 EMT 转录因子 Snail 的转录活性。我们之前已经证明了 EMT 转录因子和钙黏蛋白转换在各种临床病理分子亚型的室管膜瘤(EPN)中存在差异上调。为了分析 TRERNA1 在 EPN 中的表达相关性,我们对 75 例 2/3 级 EPN 进行了 TRERNA1 的基因表达分析,并与肿瘤部位、C11orf95-RELA 融合、年龄、MIB-1 增殖指数以及有条件的生存结果相关联。颅内 EPN 中可见 TRERNA1 基因表达水平上调,其中儿童后颅窝 EPN 中的表达水平最高。高 TRERNA1 表达与较高的增殖指数(p=0.034)和较短的无进展生存期(p=0.002)相关。我们的研究首次证明了 TRERNA1 表达与儿童后颅窝 EPN 之间存在关联。需要进一步的体内和体外研究来证实这些发现,并评估 TRERNA1 作为儿童 PF-EPN 中的新型生物标志物和潜在治疗靶点的可能性。