| Literature DB >> 31698538 |
Alessia Fabbri1, Sara Travaglione1, Francesca Rosadi1, Giulia Ballan1, Zaira Maroccia1, Massimo Giambenedetti1, Marco Guidotti2, Niels Ødum3, Thorbjørn Krejsgaard3, Carla Fiorentini1,4.
Abstract
Some toxigenic bacteria produce protein toxins with carcinogenic signatures, which either directly damage DNA or stimulate signalling pathways related to cancer. So far, however, only a few of them have been proved to favour the induction or progression of cancer. In this work, we report that the Rho-activating Escherichia coli protein toxin, cytotoxic necrotising factor 1 (CNF1), induces epithelial to mesenchymal transition (EMT) in intestinal epithelial cells. EMT is a crucial step in malignant tumour conversion and invasiveness. In the case of CNF1, it occurs by up-regulation of the transcription factors ZEB1 and Snail1, delocalisation of E-cadherin and β-catenin, activation of the serine/threonine kinase mTOR, accelerated wound healing, and invasion. However, our results highlight that nontransformed epithelial cells entail the presence of inflammatory factors, in addition to CNF1, to acquire a mesenchymal-like behaviour. All this suggests that the surrounding microenvironment, as well as the cell type, dramatically influences the CNF1 ability to promote carcinogenic traits.Entities:
Keywords: Rho GTPases; cancer; mTOR; nontransformed cell; transformed cell; virulence factors
Mesh:
Substances:
Year: 2019 PMID: 31698538 DOI: 10.1111/cmi.13138
Source DB: PubMed Journal: Cell Microbiol ISSN: 1462-5814 Impact factor: 3.715