4.8 Article

Tracing the cis-regulatory changes underlying the endometrial control of placental invasion

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.2111256119

关键词

cancer malignancy; evolution of cancer; placenta; endometrium; stomal invasibility

资金

  1. National Cancer Institute (NCI) [R37CA248161-01]
  2. NCI Center for Systems Biology at Yale [U54CA209992]

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This study investigates the genomic mechanisms underlying interspecies differences in stromal invasibility, identifying transcription factors GATA2 and TFDP1 as key regulators of fibroblast invasibility. These findings provide insights into the regulation of placental invasion, wound healing, and cancer dissemination through targeting stromal characteristics.
Among eutherian (placental) mammals, placental embedding into the maternal endometrium exhibits great differences, from being deeply invasive (e.g., humans) to noninvasive (e.g., cattle). The degree of invasion of placental trophoblasts is positively correlated with the rate of cancer malignancy. Previously, we have shown that fibroblasts from different species offer different levels of resistance to the invading trophoblasts as well as to cancer cell invasion. Here we present a comparative genomic investigation revealing cis-regulatory elements underlying these interspecies differences in invasibility. We identify transcription factors that regulate proinvasibility and antiinvasibility genes in stromal cells. Using an in vitro invasibility assay combined with CRISPR-Cas9 gene knockout, we found that the transcription factors GATA2 and TFDP1 strongly influence the invasibility of endometrial and skin fibroblasts. This work identifies genomic mechanisms explaining species differences in stromal invasibility, paving the way to therapies targeting stromal characteristics to regulate placental invasion, wound healing, and cancer dissemination.

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