MiR-1204 promotes ovarian squamous cell carcinoma growth by increasing glucose uptake

Biosci Biotechnol Biochem. 2019 Jan;83(1):123-128. doi: 10.1080/09168451.2018.1527208. Epub 2018 Oct 10.

Abstract

MiR-1204 has been recently identified as an oncogenic miRNA in breast cancer. Our study aims to investigate the role of miR-1204 in ovarian squamous cell carcinoma. Expression of miR-1204 and glucose transporter 1 in ovarian biopsies and plasma of both OC patients and healthy controls was detected by qRT-PCR. Correlations between patients' clinicopathological data were analyzed by Chi-square test. MiR-1204 overexpression OC cell lines were established. Expression of GLUT-1 protein was detected by western blot. Glucose uptake was measured by glucose uptake assay. Cell proliferation was detected by CCK-8 assay. We found that miR-1204 expression was significantly correlated with tumor size. Expression levels of miR-1204 and GLUT-1 were significantly high in OC patients. Expression levels of miR-1204 were positively correlated with expression levels of GLUT-1 in OC patients. MiR-1204 overexpression significantly promoted GLUT-1 expression, glucose uptake and cell proliferation. MiR-1204 may promote ovarian squamous cell carcinoma growth by increasing glucose uptake.

Keywords: Ovarian squamous cell carcinoma; glucose transporter 1; miR-1204; proliferation.

MeSH terms

  • Adult
  • Aged
  • Biological Transport / genetics
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology*
  • Case-Control Studies
  • Cell Proliferation / genetics
  • Drosophila Proteins / genetics
  • Female
  • Gene Expression Regulation, Neoplastic
  • Glucose / metabolism*
  • Glucose Transporter Type 1 / genetics
  • Humans
  • MicroRNAs / genetics*
  • Middle Aged
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology*
  • Transcription Factor TFIIH / genetics
  • Tumor Burden / genetics

Substances

  • Drosophila Proteins
  • Glucose Transporter Type 1
  • MIRN-1204 microRNA, human
  • MicroRNAs
  • mrn protein, Drosophila
  • Transcription Factor TFIIH
  • Glucose