GATA4 regulates the transcription of MMP9 to suppress the invasion and migration of breast cancer cells via HDAC1-mediated p65 deacetylation

Cell Death Dis. 2024 Apr 23;15(4):289. doi: 10.1038/s41419-024-06656-z.

Abstract

GATA-binding protein 4 (GATA4) is recognized for its significant roles in embryogenesis and various cancers. Through bioinformatics and clinical data, it appears that GATA4 plays a role in breast cancer development. Yet, the specific roles and mechanisms of GATA4 in breast cancer progression remain elusive. In this study, we identify GATA4 as a tumor suppressor in the invasion and migration of breast cancer. Functionally, GATA4 significantly reduces the transcription of MMP9. On a mechanistic level, GATA4 diminishes MMP9 transcription by interacting with p65 at the NF-κB binding site on the MMP9 promoter. Additionally, GATA4 promotes the recruitment of HDAC1, amplifying the bond between p65 and HDAC1. This leads to decreased acetylation of p65, thus inhibiting p65's transcriptional activity on the MMP9 promoter. Moreover, GATA4 hampers the metastasis of breast cancer in vivo mouse model. In summary, our research unveils a novel mechanism wherein GATA4 curtails breast cancer cell metastasis by downregulating MMP9 expression, suggesting a potential therapeutic avenue for breast cancer metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Breast Neoplasms* / genetics
  • Breast Neoplasms* / metabolism
  • Breast Neoplasms* / pathology
  • Cell Line, Tumor
  • Cell Movement* / genetics
  • Female
  • GATA4 Transcription Factor* / genetics
  • GATA4 Transcription Factor* / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Histone Deacetylase 1* / genetics
  • Histone Deacetylase 1* / metabolism
  • Humans
  • Matrix Metalloproteinase 9* / genetics
  • Matrix Metalloproteinase 9* / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Invasiveness*
  • Promoter Regions, Genetic / genetics
  • Transcription Factor RelA / metabolism
  • Transcription, Genetic

Substances

  • GATA4 Transcription Factor
  • Matrix Metalloproteinase 9
  • Histone Deacetylase 1
  • GATA4 protein, human
  • MMP9 protein, human
  • HDAC1 protein, human
  • Transcription Factor RelA