Associations of CTCF and FOXA1 with androgen and IGF pathways in men with localized prostate cancer

Growth Horm IGF Res. 2023 Apr-Jun:69-70:101533. doi: 10.1016/j.ghir.2023.101533. Epub 2023 Apr 14.

Abstract

Aims: To examine associations between the transcription factors CCCTC-binding factor (CTCF) and forkhead box protein A1 (FOXA1) and the androgen receptor (AR) and their association with components of the insulin-like growth factor (IGF)-pathway in a cohort of men with localized prostate cancer.

Methods: Using prostate tissue samples collected during the Prostate cancer: Evidence of Exercise and Nutrition Trial (PrEvENT) trial (N = 70 to 92, depending on section availability), we assessed the abundance of CTCF, FOXA1, AR, IGFIR, p-mTOR, PTEN and IGFBP-2 proteins using a modified version of the Allred scoring system. Validation studies were performed using large, publicly available datasets (TCGA) (N = 489).

Results: We identified a strong correlation between CTCF and AR staining with benign prostate tissue. CTCF also strongly associated with the IGFIR, with PTEN and with phospho-mTOR. FOXA1 was also correlated with staining for the IGF-IR, with IGFBP-2 and with staining for activated phosphor-mTOR. The staining for the IGF-IR was strongly correlated with the AR.

Conclusion: Our findings emphasise the close and complex links between the endocrine controls, well known to play an important role in prostate cancer, and the transcription factors implicated by the recent genetic evidence.

Keywords: Androgen signaling; CTCF; FOXA1; IGF; Prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens
  • CCCTC-Binding Factor / genetics
  • Cell Line, Tumor
  • Hepatocyte Nuclear Factor 3-alpha / genetics
  • Hepatocyte Nuclear Factor 3-alpha / metabolism
  • Humans
  • Insulin-Like Growth Factor Binding Protein 2 / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Prostatic Neoplasms* / genetics
  • Prostatic Neoplasms* / metabolism
  • Somatomedins* / genetics
  • Somatomedins* / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Androgens
  • Insulin-Like Growth Factor Binding Protein 2
  • CCCTC-Binding Factor
  • Somatomedins
  • TOR Serine-Threonine Kinases
  • Insulin-Like Growth Factor I
  • FOXA1 protein, human
  • Hepatocyte Nuclear Factor 3-alpha