Non-genomic signaling of steroid receptors in cancer

Mol Cell Endocrinol. 2021 Dec 1:538:111453. doi: 10.1016/j.mce.2021.111453. Epub 2021 Sep 11.

Abstract

Steroid receptors (SRs) are members of the nuclear receptor family, which are ligand-activated transcription factors. SRs regulate many physiological functions including development and reproduction, though they can also be involved in several pathologies, especially cancer. Highly controlled cellular responses to steroids involve transcriptional regulation (genomic activity) combined with direct activation of signaling cascades (non-genomic activity). Non-genomic signaling has been extensively studied in cancer, mainly in breast cancer for ER and PR, and prostate cancer for AR. Even though most of the studies have been conducted in cells, some of them have been confirmed in vivo, highlighting the relevance of this pathway in cancer. This review provides an overview of the current and emerging knowledge on non-genomic signaling with a focus on breast and prostate cancers and its clinical relevance. A thorough understanding of ER, PR, AR and GR non-genomic pathways may open new perspectives for the development of therapeutic strategies.

Keywords: Androgen receptor; ERα36; Estrogen receptor; Glucocorticoid receptor; Non-genomic signaling; Progesterone receptor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Breast Neoplasms / metabolism*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Prostatic Neoplasms / metabolism*
  • Receptors, Androgen / metabolism
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / metabolism
  • Receptors, Steroid / metabolism*
  • Signal Transduction

Substances

  • AR protein, human
  • Receptors, Androgen
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Receptors, Steroid