GATA4 regulates the transcription of MMP9 to suppress the invasion and migration of breast cancer cells via HDAC1-mediated p65 deacetylation
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...
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Veröffentlicht in: | Cell death & disease 2024-04, Vol.15 (4), p.289-13, Article 289 |
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Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 2041-4889 2041-4889 |
DOI: | 10.1038/s41419-024-06656-z |