LINC00662 promotes gastric cancer cell growth by modulating the Hippo-YAP1 pathway

Biochem Biophys Res Commun. 2018 Nov 2;505(3):843-849. doi: 10.1016/j.bbrc.2018.09.191. Epub 2018 Oct 6.

Abstract

Long non-coding RNAs (lncRNAs) function as vital regulators of the progression of various diseases, particularly cancers. In the present study, utilizing the Cancer Genome Atlas (TCGA) data set and a series of cell experiments and clinical tissue samples assays, we found that LINC00662 expression was significantly up-regulated in gastric cancer (GC) tissues and cell lines. High expression of LINC00662 predicted poor prognosis compared to in patients showing low expression. Knockdown of LINC00662 expression decreased GC cell proliferation and increased the chemo-sensitivity of GC cells. Further, we demonstrated that knockdown of LINC00662 suppressed the Hippo-YAP1 signaling pathway in GC cells. Mechanistically, LINC00662 regulated YAP1-mediated GC cell proliferation by sponging miR-497-5p. Overall, our results revealed a critical role for the LINC00662-miR-497-5p-YAP1 axis in GC cell growth, providing a new target for GC.

Keywords: Gastric cancer; Hippo; LINC00662; miR-497-5p.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Adaptor Proteins, Signal Transducing / physiology
  • Cell Line, Tumor
  • Cell Proliferation
  • Hippo Signaling Pathway
  • Humans
  • MicroRNAs / metabolism
  • MicroRNAs / physiology
  • Phosphoproteins / metabolism*
  • Phosphoproteins / physiology
  • Prognosis
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Serine-Threonine Kinases / physiology
  • RNA, Long Noncoding / analysis*
  • RNA, Long Noncoding / pharmacology
  • Stomach Neoplasms / pathology*
  • Transcription Factors
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • MIRN497 microRNA, human
  • MicroRNAs
  • Phosphoproteins
  • RNA, Long Noncoding
  • Transcription Factors
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • Protein Serine-Threonine Kinases