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纤维板层型肝细胞癌中的非编码RNA分析

Non coding RNA analysis in fibrolamellar hepatocellular carcinoma.

作者信息

Farber Benjamin A, Lalazar Gadi, Simon Elana P, Hammond William J, Requena David, Bhanot Umesh K, La Quaglia Michael P, Simon Sanford M

机构信息

Laboratory of Cellular Biophysics, The Rockefeller University, New York, 10065 NY, USA.

Division of Pediatric Surgery, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, 10065 NY, USA.

出版信息

Oncotarget. 2017 Dec 15;9(12):10211-10227. doi: 10.18632/oncotarget.23325. eCollection 2018 Feb 13.

Abstract

Fibrolamellar hepatocellular carcinoma (FLC) is a rare primary liver cancer found in adolescents and young adults without underlying liver disease. A deletion of ~400 kD has been found in one copy of chromosome 19 in the tumor tissue of all patients tested. This produces a fusion of the genes DNAJB1 and PRKACA which, in turn, produces a chimeric transcript and protein. Transcriptomic analysis of the tumor has shown upregulation of various oncologically relevant pathways, including EGF/ErbB, Aurora Kinase A, pak21 and wnt. To explore other factors that may contribute to oncogenesis, we examined the microRNA (miRNA) and long non-coding RNA (lncRNA) expression in FLC. The non-coding RNA expression profile in tumor tissue samples is distinctly different from the adjacent normal liver and from other liver tumors. Furthermore, miRZip knock down or over expression of certain miRNAs led to changes in the levels of coding genes that recapitulated changes observed in FLC, suggesting mechanistically that the changes in the cellular levels of miRNA are not merely correlative. Thus, in addition to serving as diagnostic tools for FLC, non-coding RNAs may serve as therapeutic targets.

摘要

纤维板层状肝细胞癌(FLC)是一种罕见的原发性肝癌,见于无潜在肝脏疾病的青少年和青年成人。在所有接受检测的患者肿瘤组织中,19号染色体的一个拷贝中发现了约400 kD的缺失。这导致DNAJB1和PRKACA基因融合,进而产生嵌合转录本和蛋白质。对肿瘤的转录组分析显示,包括EGF/ErbB、极光激酶A、pak21和wnt在内的各种肿瘤相关通路上调。为了探索可能促成肿瘤发生的其他因素,我们检测了FLC中微小RNA(miRNA)和长链非编码RNA(lncRNA)的表达。肿瘤组织样本中的非编码RNA表达谱与相邻正常肝脏以及其他肝脏肿瘤明显不同。此外,miRZip敲低或某些miRNA的过表达导致编码基因水平发生变化,重现了在FLC中观察到的变化,从机制上表明miRNA细胞水平的变化不仅仅是相关性的。因此,除了作为FLC的诊断工具外,非编码RNA还可能作为治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ad6/5828204/f8efbc37502f/oncotarget-09-10211-g001.jpg

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