| Literature DB >> 27592063 |
Tian Yang1, Hongmei Zeng2, Wanqing Chen3, Rongshou Zheng3, Yang Zhang1, Zhexuan Li1, Jun Qi4, Minjie Wang4, Tianhui Chen5, Jianlin Lou6, Lingeng Lu7, Tong Zhou1, Shuyang Dai8, Meng Cai8, Weicheng You1, Kaifeng Pan9.
Abstract
Gastric cancer (GC) is a consequence of multifactorial and multistep processes. Helicobacter pylori (H. pylori) infection plays a crucial role in gastric carcinogenesis. Long non-coding RNAs (lncRNAs) have shown great potential as powerful cancer biomarkers. To investigate the possible roles of lncRNAs and H. pylori infection in GC development, we measured expression levels of three lncRNAs (H19, LINC00152, uc001lsz) in serum from a total of 285 Chinese participants using reverse transcription-quantitative polymerase chain reaction. We found significant associations between high expression of both H19 and LINC00152 in serum and increased risk of GC; the adjusted OR for H19 was 2.17 (95% CI: 1.21-3.88), and for LINC00152 was 2.09 (95% CI: 1.18-3.70). Further analyses indicated an elevated risk of GC in subjects with both high H19 expression and H. pylori infection (OR: 13.75, 95% CI: 4.75-39.84). Significant joint effect between LINC00152 and H. pylori infection on risk of GC was also found (OR: 17.49, 95% CI: 4.78-63.92). Serum H19 and LINC00152 may serve as potential biomarkers for diagnosis of GC, particularly for those with H. pylori infection.Entities:
Keywords: Biomarkers; Gastric cancer; Helicobacter pylori; Long non-coding RNA; Serum
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Year: 2016 PMID: 27592063 DOI: 10.1016/j.canep.2016.08.015
Source DB: PubMed Journal: Cancer Epidemiol ISSN: 1877-7821 Impact factor: 2.984