| Literature DB >> 29403038 |
Olivier Zajac1,2, Joel Raingeaud1, Fotine Libanje1, Celine Lefebvre1, Dora Sabino1, Isabelle Martins3,4, Pétronille Roy1, Clara Benatar1, Charlotte Canet-Jourdan1, Paula Azorin1, Mélanie Polrot5, Patrick Gonin5, Salima Benbarche6, Sylvie Souquere7, Gerard Pierron7, Damien Nowak1, Ludovic Bigot1, Michel Ducreux8, David Malka8, Camille Lobry6, Jean-Yves Scoazec9, Clarisse Eveno10, Marc Pocard10, Jean-Luc Perfettini3,4, Dominique Elias8, Peggy Dartigues9, Diane Goéré8, Fanny Jaulin11.
Abstract
Metastases account for 90% of cancer-related deaths; thus, it is vital to understand the biology of tumour dissemination. Here, we collected and monitored >50 patient specimens ex vivo to investigate the cell biology of colorectal cancer (CRC) metastatic spread to the peritoneum. This reveals an unpredicted mode of dissemination. Large clusters of cancer epithelial cells displaying a robust outward apical pole, which we termed tumour spheres with inverted polarity (TSIPs), were observed throughout the process of dissemination. TSIPs form and propagate through the collective apical budding of hypermethylated CRCs downstream of canonical and non-canonical transforming growth factor-β signalling. TSIPs maintain their apical-out topology and use actomyosin contractility to collectively invade three-dimensional extracellular matrices. TSIPs invade paired patient peritoneum explants, initiate metastases in mice xenograft models and correlate with adverse patient prognosis. Thus, despite their epithelial architecture and inverted topology TSIPs seem to drive the metastatic spread of hypermethylated CRCs.Entities:
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Year: 2018 PMID: 29403038 DOI: 10.1038/s41556-017-0027-6
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824