Association between expression of TNF-α, P53 and HIF1α with asthenozoospermia

Hum Fertil (Camb). 2019 Jun;22(2):145-151. doi: 10.1080/14647273.2018.1493750. Epub 2018 Sep 17.

Abstract

Reduced sperm motility (asthenozoospermia) accounts for a significant percentage of male infertility and numerous factors have been suggested to explain this phenomenon among which hypoxic and inflammatory markers are the least studied. Therefore, the aim of this study was to assess the main molecular markers involved in hypoxia (P53 and HIF-1α) and inflammation (TNF-α) pathways in infertile men with asthenozoospermia. Expression of these markers were assessed by qRT-PCR, and analysis of data show that mean of hypoxia markers (P53, HIF-1α) and also TNF- α were significantly higher in infertile men with asthenozoospermia compared to fertile men (p < 0.05). Unlike TNF-α, significant negative correlations were observed between expression of P53 (r = -0.568; p = 0.002) and HIF-1α (r = -0.403; p = 0.046) with sperm motility. In addition, a significant negative correlation was observed between expression of P53 with sperm concentration (r = -0.576; p < 0.001). In addition, a significant positive correlation was observed between hypoxia markers (P53, HIF-1α) and TNF-α (p < 0.01). However, no significant relation was observed between TNF-α and semen parameters. Taken together, the results of this study suggest the involvement of hypoxia pathway is more pronounced than the inflammatory pathway in asthenozoospermia.

Keywords: Asthenozoospermia; HIF-1α; P53; TNF-α; sperm parameters.

MeSH terms

  • Adult
  • Aged
  • Asthenozoospermia / genetics*
  • Gene Expression Regulation / physiology*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Infertility, Male / genetics
  • Male
  • Middle Aged
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Tumor Suppressor Protein p53