Increased Expression of Follistatin in Breast Cancer Reduces Invasiveness and Clinically Correlates with Better Survival

Cancer Genomics Proteomics. 2017 Jul-Aug;14(4):241-251. doi: 10.21873/cgp.20035.

Abstract

Background/aim: Activin and its antagonist follistatin (FST) have been implicated in several solid tumours. This study investigated the role of FST in breast cancer.

Materials and methods: FST expression was examined using reverse transcription polymerase chain reaction (RT-PCR), real-time quantitative polymerase chain reaction (qPCR) and immunohistochemistry in a cohort of breast cancer samples. Expression was correlated to pathological and prognostic parameters in our patient cohort. FST was overexpressed in MCF-7 cells and assays for growth and invasion were performed.

Results: FST is expressed in breast tissue, in the cytoplasm of mammary epithelial cells. Expression was decreased in breast cancer tissue in comparison to normal mammary tissue. Over-expression of FST in vitro led to significantly increased growth rate and reduced invasion. Higher FST associates with lower-grade tumours and better survival.

Conclusion: Our results suggest a role for FST as a suppressor of invasion and metastasis in breast cancer.

Keywords: Follistatin; breast cancer; survival.

MeSH terms

  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Proliferation
  • Cohort Studies
  • Female
  • Follistatin / metabolism*
  • Humans
  • MCF-7 Cells
  • Neoplasm Invasiveness*
  • Survival Analysis

Substances

  • Follistatin