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

Proc Natl Acad Sci U S A. 2022 Feb 8;119(6):e2111256119. doi: 10.1073/pnas.2111256119.

Abstract

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.

Keywords: cancer malignancy; endometrium; evolution of cancer; placenta; stomal invasibility.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • CRISPR-Cas Systems
  • Cell Line, Tumor
  • Endometrium / metabolism*
  • Endometrium / pathology
  • Female
  • GATA2 Transcription Factor / genetics
  • GATA2 Transcription Factor / metabolism
  • Gene Knockout Techniques
  • Humans
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Transcription Factor DP1 / metabolism
  • Trophoblasts / metabolism*
  • Trophoblasts / pathology

Substances

  • GATA2 Transcription Factor
  • GATA2 protein, human
  • Neoplasm Proteins
  • TFDP1 protein, human
  • Transcription Factor DP1