Microarray analysis of Long non-coding RNA expression profiles in human gastric cells and tissues with Helicobacter pylori Infection

• Published in: BMC medical genomics Vol. 8; no. 84; p. 84
• Main Authors: Zhu, Hong, Wang, Qiang, Yao, Yizheng, Fang, Jian, Sun, Fengying, Ni, Ying, Shen, Yixin, Wang, Hua, Shao, Shihe
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 21-12-2015; BioMed Central
• Subjects: Analysis; Care and treatment; Cell Line; DNA microarrays; Epithelial Cells - metabolism; Epithelial Cells - microbiology; Gene Expression Profiling; Gene Ontology; Genetic aspects; Helicobacter infections; Helicobacter pylori; Helicobacter pylori - physiology; Humans; Messenger RNA; Oligonucleotide Array Sequence Analysis; RNA, Long Noncoding - genetics; RNA, Messenger - genetics; Stomach - cytology; Stomach - metabolism; Stomach - microbiology; China
• ISSN: 1755-8794; 1755-8794
• DOI: 10.1186/s12920-015-0159-0

Although Helicobacter pylori (H.pylori) is the dominant gastrointestinal pathogen, the genetic and molecular mechanisms underlying H.pylori-related diseases have not been fully elucidated. Long non-coding RNAs (lncRNAs) have been identified in eukaryotic cells, many of which play important roles in regulating biological processes and pathogenesis. However, the expression changes of lncRNAs in human infected by H.pylori have been rarely reported. This study aimed to identify the dysregulated lncRNAs in human gastric epithelial cells and tissues infected with H.pylori.
The aberrant expression profiles of lncRNAs and mRNAs in GES-1 cells with or without H.pylori infection were explored by microarray analysis. LncRNA-mRNA co-expression network was constructed based on Pearson correlation analysis. Gene Ontology (GO) and KEGG Pathway analyses of aberrantly expressed mRNAs were performed to identify the related biological functions and pathologic pathways. The expression changes of target lncRNAs were validated by qRT-PCR to confirm the microarray data in both cells and clinical specimens.
Three hundred three lncRNAs and 565 mRNAs were identified as aberrantly expressed transcripts (≥2 or ≤0.5-fold change, P < 0.05) in cells with H.pylori infection compared to controls. LncRNA-mRNA co-expression network showed the core lncRNAs/mRNAs which might play important roles in H.pylori-related pathogenesis. GO and KEGG analyses have indicated that the functions of aberrantly expressed mRNAs in H.pylori infection were related closely with inflammation and carcinogenesis. QRT-PCR data confirmed the expression pattern of 8 (n345630, XLOC_004787, n378726, LINC00473, XLOC_005517, LINC00152, XLOC_13370, and n408024) lncRNAs in infected cells. Additionally, four down-regulated (n345630, XLOC_004787, n378726, and LINC00473) lncRNAs were verified in H.pylori-positive gastric samples.
Our study provided a preliminary exploration of lncRNAs expression profiles in H.pylori-infected cells by microarray. These dysregulated lncRNAs might contribute to the pathological processes during H.pylori infection.