Pioneer factor GATA6 promotes colorectal cancer through 3D genome regulation

Colorectal cancer (CRC) is one of the most lethal and prevalent malignancies. While the overexpression of pioneer factor GATA6 in CRC has been linked with metastasis, its role in genome-wide gene expression dysregulation remains unclear. Through studies of primary human CRC tissues and analysis of the TCGA data, we found that GATA6 preferentially binds at CRC-specific active enhancers, with enrichment at enhancer-promoter loop anchors. GATA6 protein also physically interacts with CTCF, suggesting its critical role in 3D genome organization. The ablation of GATA6 through AID and CRISPR systems severely impaired cancer cell clonogenicity and proliferation. Mechanistically, GATA6 knockout induced global loss of CRC-specific open chromatins and extensive alterations of critical enhancer-promoter interactions for CRC oncogenes. Last, we showed that GATA6 knockout greatly reduced tumor growth and improved survival in mice. Together, we revealed a previously unidentified mechanism by which GATA6 contributes to the pathogenesis of colorectal cancer.

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Publication Details

Journal
Science Advances
Published
2025-02-07
DOI
https://doi.org/10.1126/sciadv.ads4985
Citations
6
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
4.84

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article

Pioneer factor GATA6 promotes colorectal cancer through 3D genome regulation

Guang‐Yu Yang, Lena Stasiak, Josiah Hiu-yuen Wong, T. Zhang et al.
6 citations
Science Advances
Epigenetics and DNA Methylation
4.84
article

Pioneer factor GATA6 promotes colorectal cancer through 3D genome regulation

Guang‐Yu Yang, Lena Stasiak, Josiah Hiu-yuen Wong, T. Zhang, Juan Wang, Leyu Sun, Feng Yue, Huijue Lyu, Yang Cheng, X.-X. Chen, Lu Wang, Ping Wang
article en
6 citations

Abstract

Colorectal cancer (CRC) is one of the most lethal and prevalent malignancies. While the overexpression of pioneer factor GATA6 in CRC has been linked with metastasis, its role in genome-wide gene expression dysregulation remains unclear. Through studies of primary human CRC tissues and analysis of the TCGA data, we found that GATA6 preferentially binds at CRC-specific active enhancers, with enrichment at enhancer-promoter loop anchors. GATA6 protein also physically interacts with CTCF, suggesting its critical role in 3D genome organization. The ablation of GATA6 through AID and CRISPR systems severely impaired cancer cell clonogenicity and proliferation. Mechanistically, GATA6 knockout induced global loss of CRC-specific open chromatins and extensive alterations of critical enhancer-promoter interactions for CRC oncogenes. Last, we showed that GATA6 knockout greatly reduced tumor growth and improved survival in mice. Together, we revealed a previously unidentified mechanism by which GATA6 contributes to the pathogenesis of colorectal cancer.

Science AdvancesVol. 11(6)
Northwestern University (US)
Northwestern University
Good health and well-being
Openalex Percentile: Top 5%
Epigenetics and DNA Methylation
4.84
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