Liu Yue,Chen Hongyu,Shao Qing,Mao Gaoping,Ning Shoubin,Zhang Yafei.Expression and role of long non-coding RNA LINC00261 in Barrett’s esophagus and esophageal adenocarcinoma[J].J Amry Med Univ (J Third Mil Med Univ),2017,39(01):67-71.
Liu Yue,Chen Hongyu,Shao Qing,Mao Gaoping,Ning Shoubin,Zhang Yafei.Expression and role of long non-coding RNA LINC00261 in Barrett’s esophagus and esophageal adenocarcinoma[J].J Amry Med Univ (J Third Mil Med Univ),2017,39(01):67-71.DOI:
Objective To evaluate the expression of long non-coding RNA
LINC00261
in Barrett’s esophagus and esophageal adenocarcinoma
and to investigate its possible mechanism. Methods qRT-PCR was used to analyze the expression levels of LINC00261 in normal esophageal squamous epithelium
Barrett’s esophagus and esophageal adenocarcinoma of Chinese population. The possible role of LINC00261 in the development of Barrett’s esophagus was investigated in human embryonic stem cells. Results The expression level of LINC00261 were significantly higher in the Barrett’s esophagus and esophageal adenocarcinoma than the normal esophageal squamous epithelium tissues (P0.01). Acid and bile exposure enhanced the expression of LINC00261 and inhibited the protein level of FOXA2 in human embryonic stem cells. While lentivirus-mediated up-regulation of LINC00261 also induced the inhibition of FOXA2 expression. What’s more
FOXA2 up-regulation blocked the expression of CDX2 and differentiation phenotype (expression of MUC2
a biomarker for columnar differentiation) in human embryonic stem cells induced by acid and bile exposure. Conclusion LINC00261 plays a key role in the development of Barrett’s esophagus
and FOXA2 is involved in the related regulation by inhibiting FOXA2.