Liu Dong, Dong Yinghui, Gao Jiahui, Wu Zhouguang, Zhang Lihui, Wang Bin
Department of General Surgery, Shenzhen Children's Hospital, Shenzhen, Guangdong 518000, P.R. China.
Department of Ultrasound, Shenzhen People's Hospital, Shenzhen, Guangdong 518000, P.R. China.
Exp Ther Med. 2024 Jan 9;27(3):95. doi: 10.3892/etm.2024.12383. eCollection 2024 Mar.
Circular RNAs (circRNAs) serve an essential role in the occurrence and development of cholangiocarcinoma, but the expression and function of circRNA in biliary atresia (BA) is not clear. In the present study, circRNA expression profiles were investigated in the liver tissues of patients with BA as well as in the choledochal cyst (CC) tissues of control patients using RNA sequencing. A total of 78 differentially expressed circRNAs (DECs) were identified between the BA and CC tissues. The expression levels of eight circRNAs (hsa_circ_0006137, hsa_circ_0079422, hsa_circ_0007375, hsa_circ_0005597, hsa_circ_0006961, hsa_circ_0081171, hsa_circ_0084665 and hsa_circ_0075828) in the liver tissues of the BA group and control group were measured using reverse transcription-quantitative polymerase chain reaction. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis demonstrated that the identified DECs are involved in a variety of biological processes, including apoptosis and metabolism. In addition, based on the GO and KEGG pathway enrichment analyses, it was revealed that target genes that can be affected by circRNAs regulatory network were enriched in the TGF-β signaling pathway, EGFR tyrosine kinase inhibitor resistance pathway and transcription factor regulation pathway as well as other pathways that may be associated with the pathogenesis of BA. The present study revealed that circRNAs are potentially implicated in the pathogenesis of BA and could help to find promising targets and biomarkers for BA.
环状RNA(circRNAs)在胆管癌的发生和发展中起重要作用,但circRNA在胆道闭锁(BA)中的表达和功能尚不清楚。在本研究中,使用RNA测序技术对BA患者的肝组织以及对照患者的胆总管囊肿(CC)组织中的circRNA表达谱进行了研究。在BA组织和CC组织之间共鉴定出78种差异表达的circRNA(DECs)。使用逆转录-定量聚合酶链反应检测了BA组和对照组肝组织中8种circRNA(hsa_circ_0006137、hsa_circ_0079422、hsa_circ_0007375、hsa_circ_0005597、hsa_circ_0006961、hsa_circ_0081171、hsa_circ_0084665和hsa_circ_0075828)的表达水平。基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析表明,鉴定出的DECs参与了多种生物学过程,包括细胞凋亡和代谢。此外,基于GO和KEGG通路富集分析,发现受circRNAs调控网络影响的靶基因在TGF-β信号通路、EGFR酪氨酸激酶抑制剂抗性通路和转录因子调控通路以及其他可能与BA发病机制相关的通路中富集。本研究表明,circRNAs可能与BA的发病机制有关,并有助于寻找有前景的BA靶点和生物标志物。