Expression and clinical significance of hypoxia-inducible factor 1α, Snail and E-cadherin in human ovarian cancer cell lines

Mol Med Rep. 2015 Sep;12(3):3393-3399. doi: 10.3892/mmr.2015.3786. Epub 2015 May 14.

Abstract

The aim of the present study was to investigate the expression and clinical significance of hypoxia-inducible factor 1α (HIF-1α), Snail and E-cadherin in ovarian cancer. The expression levels were assessed in a number of ovarian cancer cell lines and ovarian cancer tissues, and correlations between the expression of the three proteins and clinical pathological factors were analyzed. Transwell assays showed that the invasive ability of the ovarian cancer cell lines SKOV3 and ES‑2 were significantly higher than those of TYK and 3AO (P<0.01). Furthermore, the expression levels of HIF‑1α and Snail in SKOV3 and ES‑2 were significantly higher than those in TYK and 3AO, whereas the expression levels of E‑cadherin in SKOV3 and ES‑2 were significantly lower than those in TYK and 3AO (P<0.05). In ovarian cancer tissues, the expression levels of HIF‑1α, Snail and E‑cadherin were correlated with clinical pathological factors (P<0.01); furthermore, there was a positive correlation between the expression levels of HIF‑1α and Snail (r=0.231; P=0.021), and a negative correlation between the expression levels of Snail and that of E‑cadherin (r=‑0.225; P=0.028). HIF‑1α was suggested to be able to suppress the expression of E‑cadherin by upregulating Snail, thus serving an important role in invasion and metastasis of ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, CD
  • Cadherins / genetics
  • Cadherins / metabolism*
  • Cell Line, Tumor
  • Female
  • Gene Expression
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Lymphatic Metastasis
  • Middle Aged
  • Neoplasm Invasiveness
  • Neoplasms, Glandular and Epithelial / genetics
  • Neoplasms, Glandular and Epithelial / metabolism*
  • Neoplasms, Glandular and Epithelial / secondary
  • Ovarian Neoplasms / genetics
  • Ovarian Neoplasms / metabolism*
  • Ovarian Neoplasms / pathology
  • Snail Family Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Snail Family Transcription Factors
  • Transcription Factors