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微小RNA和竞争性内源性RNA在先天性巨结肠病(HSCR)中的致病作用:HSCR的潜在诊断标志物

Pathogenic roles of microRNAs and competing endogenous RNAs in Hirschsprung disease (HSCR): Potential diagnostic markers for HSCR.

作者信息

Hou Lian, Kang Quan

机构信息

Department of General and Trauma Surgery Children's Hospital of Chongqing Medical University National Clinical Research Center for Child Health and Disorders Ministry of Education Key Laboratory of Child Development and Disorders Chongqing China.

出版信息

Pediatr Discov. 2023 Jul 31;1(2):e21. doi: 10.1002/pdi3.21. eCollection 2023 Sep.

Abstract

MicroRNAs (miRNAs) are endogenous small non-coding single-stranded RNAs. They can bind to the 3'-untranslated region (3'UTR) of mRNAs and regulate the expression of their target genes by inducing degradation or translation inhibition of the corresponding mRNAs. Competing endogenous RNAs (ceRNAs) can disable miRNAs by combining miRNAs response elements (MREs) with miRNAs. Hirschsprung disease (HSCR) is a common pediatric surgical disease in which cells derived from the enteric neural crest fail to colonize the distal colon, but its pathogenesis is not very clear. In recent years, with more and more studies on miRNAs in HSCR, miRNAs seem to be involved in the pathogenesis of HSCR. miRNAs in HSCR affect the proliferation and migration of enteric neural crest cells mainly through target genes, and ceRNAs inhibit miRNAs, thus participating in the pathogenesis of HSCR. It was reported that some miRNAs in the serum of children with HSCR were significantly higher than those in the control group. Therefore, miRNAs are expected to be a new noninvasive early screening biomarker and targeted therapy point for HSCR. Here, we provide a summary of the understanding of miRNAs and ceRNAs in regulating enteric nervous system proliferation and migration and their roles in the pathogenesis of HSCR.

摘要

微小RNA(miRNA)是内源性小的非编码单链RNA。它们可与信使核糖核酸(mRNA)的3'非翻译区(3'UTR)结合,并通过诱导相应mRNA的降解或翻译抑制来调节其靶基因的表达。竞争性内源性RNA(ceRNA)可通过将miRNA反应元件(MRE)与miRNA结合来使miRNA失活。先天性巨结肠病(HSCR)是一种常见的儿科外科疾病,其中源自肠神经嵴的细胞无法定植于远端结肠,但其发病机制尚不完全清楚。近年来,随着对HSCR中miRNA的研究越来越多,miRNA似乎参与了HSCR的发病机制。HSCR中的miRNA主要通过靶基因影响肠神经嵴细胞的增殖和迁移,而ceRNA抑制miRNA,从而参与HSCR的发病机制。据报道,HSCR患儿血清中的一些miRNA明显高于对照组。因此,miRNA有望成为HSCR新的非侵入性早期筛查生物标志物和靶向治疗靶点。在此,我们总结了对miRNA和ceRNA在调节肠神经系统增殖和迁移及其在HSCR发病机制中的作用的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91e5/12118252/2adbd5d7ecac/PDI3-1-e21-g001.jpg

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