Xiao Jie, Xia Su-yun, Xia Yun, Xia Qiang, Wang Xiang-rui
Ren Ji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Mol Biol Rep. 2014 Dec;41(12):8063-9. doi: 10.1007/s11033-014-3704-6. Epub 2014 Sep 6.
Biliary atresia is the major kind of liver disease that mainly affects the new born infants. The pathological and biological mechanism of biliary atresia is still unclear to date. In this work, we attempt to identify biliary atresia relevant genes and to get the knowledge of the underlying genetic basis. We collected liver samples from new born infants with biliary atresia and congenital choledochocyst, and the RNA-seq technology was used to performed a transcriptome profiling in order to comprehensively study their expression signatures. We identified 877 differentially expressed genes between samples from biliary atresia and congenital choledochocyst patients in total. Several biological pathways related to the immunity and inflammation response were found to involve in the development of biliary atresia. Our results may helps to better investigate the molecular mechanisms of this disease.
胆道闭锁是主要影响新生儿的一种主要肝脏疾病。迄今为止,胆道闭锁的病理和生物学机制仍不清楚。在这项工作中,我们试图识别与胆道闭锁相关的基因,并了解其潜在的遗传基础。我们收集了患有胆道闭锁和先天性胆总管囊肿的新生儿的肝脏样本,并使用RNA测序技术进行转录组分析,以全面研究它们的表达特征。我们总共在胆道闭锁患者和先天性胆总管囊肿患者的样本之间鉴定出877个差异表达基因。发现一些与免疫和炎症反应相关的生物学途径参与了胆道闭锁的发展。我们的结果可能有助于更好地研究这种疾病的分子机制。