4.6 Article

Long Non-Coding RNA GRIK1-AS1 Inhibits the Proliferation and Invasion of Gastric Cancer Cells by Regulating the miR-375/IFIT2 Axis

期刊

FRONTIERS IN ONCOLOGY
卷 11, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.754834

关键词

long non-coding RNA; lncRNA GRIK1-AS1; miR-375; IFIT2; gastric cancer

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资金

  1. National Natural Science Foundation of China [31570877, 31800745]
  2. Key R&D Project of Science and Technology Department of Jiangsu Province [BE2016660, BE2018645]
  3. Changzhou High-Level Medical Talents Training Project [2016CZBJ001]
  4. Scientific and Technological Support Program for Social Development of Changzhou Sci and Tech Bureau [CE20215042]

向作者/读者索取更多资源

This study identified the regulatory relationship between lncRNA GRIK1-AS1 and the miR-375/IFIT2 axis in gastric cancer. It demonstrated that GRIK1-AS1 acts as a sponge for miR-375, impacting the progression of gastric cancer by modulating target mRNA IFIT2 translation. These findings provide a novel strategy for future therapeutic development based on GRIK1-AS1.
Long non-coding RNAs (lncRNAs) play important roles in various biological processes and human diseases, including cancer. In this study, we demonstrated a regulatory relationship between lncRNA GRIK1-AS1 and miR-375/IFIT2 axis in gastric cancer. Our results show a decreased expression of GRIK1-AS1 in gastric cancer tissues compared to adjacent normal gastric tissues. Gastric cell lines also have reduced levels of GRIK1-AS1 compared to gastric epithelial cell line GES-1. Ectopic expression of GRIK1-AS1 in gastric cancer cell lines significantly inhibits cellular viability, migration, and invasion. RNA-pull down and the luciferase activity assays show that GRIK1-AS1 mainly interacts specifically with miR-375. We further demonstrate a negatively regulatory relationship between lncRNA GRIK1-AS1 and miR-375. We discovered that IFIT2 was one of the direct key downstream target genes of miR-375, and established the important role of the GRIK1-AS1/miR-375/IFIT2 axis in the progression of gastric cancer. Taken together, our results revealed a novel mechanism of GRIK1-AS1 as a sponge to miR-375 that impacts gastric cancer progression via modulating target mRNA IFIT2 translation, and as a result, opens a new strategy to future GRIK1-AS1 based therapeutic development.

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