Nature Communications (Nov 2021)

Compressive stress-mediated p38 activation required for ERα + phenotype in breast cancer

  • Pauliina M. Munne,
  • Lahja Martikainen,
  • Iiris Räty,
  • Kia Bertula,
  • Nonappa,
  • Janika Ruuska,
  • Hanna Ala-Hongisto,
  • Aino Peura,
  • Babette Hollmann,
  • Lilya Euro,
  • Kerim Yavuz,
  • Linda Patrikainen,
  • Maria Salmela,
  • Juho Pokki,
  • Mikko Kivento,
  • Juho Väänänen,
  • Tomi Suomi,
  • Liina Nevalaita,
  • Minna Mutka,
  • Panu Kovanen,
  • Marjut Leidenius,
  • Tuomo Meretoja,
  • Katja Hukkinen,
  • Outi Monni,
  • Jeroen Pouwels,
  • Biswajyoti Sahu,
  • Johanna Mattson,
  • Heikki Joensuu,
  • Päivi Heikkilä,
  • Laura L. Elo,
  • Ciara Metcalfe,
  • Melissa R. Junttila,
  • Olli Ikkala,
  • Juha Klefström

DOI
https://doi.org/10.1038/s41467-021-27220-9
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 17

Abstract

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Reliable luminal estrogen receptor (ERα+) breast cancer models are limited. Here, the authors use patient derived breast epithelial and breast cancer explant cultures grown in several extracellular matrix scaffolds and show that ERα expression is regulated by matrix stiffness via stress-mediated p38 activation and H3K27me3-mediated epigenetic regulation.