Serum miR-658 induces metastasis of gastric cancer by activating PAX3-MET pathway: A population-based study

Cancer Biomark. 2018;22(1):111-118. doi: 10.3233/CBM-171045.

Abstract

Background and objective: MiR-658, paired box gene 3 (PAX3) and met proto-oncogene (MET) are overexpressed in gastric cancer while PAX3 and MET can be regulated by miRNA. Serum miR-658 may be associated with metastasis of gastric cancer (MGC) by affecting PAX3-MET pathway.

Methods: Ninety-eight gastric carcinoma patients with distant MGC (DM group) and ninety-six gastric carcinoma patients with no MGC (NM group) were recruited. Serum miR-658 was validated between DM and NM groups by using quantitative reverse transcription PCR (qRT-PCR). PAX3 and MET levels were measured by Western Blot. The molecular mechanism for the function of serum miR-658 was further validated in gastric cell lines.

Results: The results demonstrate that serum level of miR-658 is significantly lower in the NM group than in the DM group (P< 0.001). Meanwhile, the levels of PAX3 and MET are lower in the NM group than in the DM group too (P< 0.01). Both overexpression and silence of miR-658 significantly up-regulate or down-regulate the levels of PAX3 and MET in gastric cell lines (P< 0.05).

Conclusions: The present findings demonstrate that elevated circulating miR-658 is associated with MGC by activating PAX3-MET pathway.

Keywords: Met proto-oncogene; metastasis of gastric carcinoma; miR-658; paired box gene 3.

Publication types

  • Retracted Publication

MeSH terms

  • Case-Control Studies
  • Female
  • Humans
  • Male
  • MicroRNAs / blood*
  • Middle Aged
  • Neoplasm Metastasis
  • PAX3 Transcription Factor / blood*
  • PAX3 Transcription Factor / genetics
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-met / blood*
  • Proto-Oncogene Proteins c-met / genetics
  • Signal Transduction
  • Stomach Neoplasms / blood
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology

Substances

  • MAS1 protein, human
  • MicroRNAs
  • PAX3 Transcription Factor
  • PAX3 protein, human
  • Proto-Oncogene Mas
  • MET protein, human
  • Proto-Oncogene Proteins c-met