Preliminary screening and identification of long-chain non-coding RNA HOTAIR related to reflux esophagitis based on transcriptome sequencing

  • NIU Lu ,
  • MENG Xianmei ,
  • SHAO Guo
Expand
  • 1. Baotou Medical College, Baotou 014040, China;
    2. Department of Gastroenterology, the Second Affiliated Hospital of Baotou Medical College

Received date: 2022-03-29

  Online published: 2023-09-22

Abstract

Objective: To elucidate the differentially expressed genes in reflux esophagitis and explore the possible mechanism of mucosal damage in reflux esophagitis, and preliminarily screen and identify the expression changes and effects of long-chain non-coding RNA HOTAIR in reflux esophagitis. Methods: Transcriptome sequencing and bioinformatics analysis were performed on tissue specimens at mucosal erosion site of reflux esophagitis and mucosa smooth esophageal tissue under para-erosion endoscopy. The expression changes of long-chain non-coding RNA HOTAIR in the two types of tissues were determined by real-time fluorescent quantitative PCR, and its relationship with the age of patients with reflux esophagitis was analyzed. Results: The transcriptome sequencing results showed that there were a variety of genes differentially expressed between the erosive group and the para-erosive group of reflux esophagitis, of which 7661 genes were down-regulated. Bioinformatics analysis showed that differentially expressed genes were enriched in immune responses. For the screened long-chain non-coding RNA HOTAIR, real-time fluorescent quantitative PCR showed that its relative expression was correlated with the age of patients with reflux esophagitis (P<0.05). Compared with the para-erosion group, the expression of HOTAIR was up-regulated in the erosion group of reflux esophagitis in the older age group (P<0.05), and down-regulated in the erosion group of reflux esophagitis in the younger age group (P<0.05). Conclusion: The differentially expressed genes may be involved in the pathogenesis of reflux esophagitis through immune response. The screened long-chain non-coding RNA HOTAIR expression showed opposite trends in patients of different ages, suggesting that HOTAIR may play an important role in reflux esophagitis and can be used as an important auxiliary indicator for diagnosis.

Cite this article

NIU Lu , MENG Xianmei , SHAO Guo . Preliminary screening and identification of long-chain non-coding RNA HOTAIR related to reflux esophagitis based on transcriptome sequencing[J]. Journal of Baotou Medical College, 2023 , 39(9) : 34 -39 . DOI: 10.16833/j.cnki.jbmc.2023.09.007

References

[1] Souza RF,Huo XF,Mittal V,et al. Gastroesophageal reflux might cause esophagitis through a cytokine-mediated mechanism rather than caustic acid injury[J].Gastroenterology,2009,137(5):1776-1784.
[2] Souza RF,Bayeh L,Spechler SJ,et al. A new paradigm for GERD pathogenesis.Not acid injury,but cytokine-mediated inflammation driven by HIF-2α:a potential role for targeting HIF-2α to prevent and treat reflux esophagitis[J].Curr Opin Pharmacol,2017,37:93-99.
[3] 李毅,孙涛. 胃食管反流病发病机制研究进展[J].解放军医学院学报,2013,34(6):552-554,557.
[4] Dunbar KB,Agoston AT,Odze RD,et al. Association of acute gastroesophageal reflux disease with esophageal histologic changes[J].JAMA,2016,315(19):2104.
[5] Souza RF. Reflux esophagitis and its role in the pathogenesis of barrett's metaplasia[J].J Gastroenterol,2017,52(7):767-776.
[6] Rieder F,Biancani P,Harnett K,et al. Inflammatory mediators in gastroesophageal reflux disease:impact on esophageal motility,fibrosis,and carcinogenesis[J].Am J Physiol Gastrointest Liver Physiol,2010,298(5):G571-G581.
[7] Price RL,Bhan A,Mandal SS. HOTAIR beyond repression:in protein degradation,inflammation,DNA damage response,and cell signaling[J].DNA Repair,2021,105:103141.
[8] Zhang JH,Chen M,Zhai YY,et al. Retracted:HOTAIR regulates lipopolysaccharide-induced inflammatory response in hepatocytes[J].J Cell Physiol,2020,235(5):4247-4255.
[9] Sathishkumar C,Prabu P,Mohan V,et al. Linking a role of lncRNAs (long non-coding RNAs) with insulin resistance,accelerated senescence,and inflammation in patients with type 2 diabetes[J].Hum Genom,2018,12(1):41.
[10] Obaid M,Udden SMN,Alluri P,et al. LncRNA HOTAIR regulates glucose transporter Glut1 expression and glucose uptake in macrophages during inflammation[J].Sci Rep,2021,11(1):232.
[11] Liu J,Huang GQ,Ke ZP. Silence of long intergenic noncoding RNA HOTAIR ameliorates oxidative stress and inflammation response in ox-LDL-treated human macrophages by upregulating miR-330-5p[J].J Cell Physiol,2019,234(4):5134-5142.
[12] Su M,Xiao YH,Ma JL,et al. Long non-coding RNAs in esophageal cancer:molecular mechanisms,functions,and potential applications[J].J Hematol Oncol,2018,11(1):118.
[13] Wang AH,Tan P,Zhuang Y,et al. Down-regulation of long non-coding RNA HOTAIR inhibits invasion and migration of oesophageal cancer cells via up-regulation of microRNA-204[J].J Cell Mol Med,2019,23(10):6595-6610.
[14] Schwarzenbach H,Hoon DSB,Pantel K. Cell-free nucleic acids as biomarkers in cancer patients[J].Nat Rev Cancer,2011,11(6):426-437.
[15] Sendler E,Johnson GD,Mao SH,et al. Stability,delivery and functions of human sperm RNAs at fertilization[J].Nucleic Acids Res,2013,41(7):4104-4117.
[16] Azer SA,Reddivari A.Reflux esophagitis in:statpeals [internet] [M]. Treasure Island:startpeals publishing,2021.
[17] He J,Ma XQ,Zhao YF,et al. A population-based survey of the epidemiology of symptom-defined gastroesophageal reflux disease:the systematic investigation of gastrointestinal diseases in China[J].BMC Gastroenterol,2010,10:94.
[18] Aminian K,Mashayekhi F,Mirzanejad L,et al. A functional genetic variant in GAS5 lncRNA (rs145204276) modulates p27Kip1 expression and confers risk for gastric cancer[J].Br J Biomed Sci,2019,76(2):83-85.
[19] Santin I,JAuregi-Miguel A,Velayos T,et al. Celiac diasease–associated lncRNA named HCG14 regulates NOD1 expression in intestinal cells[J].J Pediatr Gastroenterol Nutr,2018,67(2):225-231.
[20] Kasyap AK,Sah SK,Chaudhary S. Clinical spectrum and risk factors associated with asymptomatic erosive esophagitis as determined by Los Angeles classification:a cross-sectional study[J].PLoS One,2018,13(2):e0192739.
[21] Nguyen AD,Spechler SJ,Shuler MN,et al. Unique clinical features of los angeles grade D esophagitis suggest that factors other than gastroesophageal reflux contribute to its pathogenesis[J].J Clin Gastroenterol,2019,53(1):9-14.
Outlines

/