Early functional mismatch between breast cancer cells and their tumour microenvironment suppresses long term growth.

Autor: Perdrix Rosell A; Tumour Host Interaction Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK; Sanz-Moreno Lab, Centre for Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK; Randall Division of Cell and Molecular Biophysics, King's College London, New Hunt's House, Guy's Campus, London, SE1 1UL, UK., Maiques O; Sanz-Moreno Lab, Centre for Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK; Randall Division of Cell and Molecular Biophysics, King's College London, New Hunt's House, Guy's Campus, London, SE1 1UL, UK., Martin JAJ; Sanz-Moreno Lab, Centre for Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK., Chakravarty P; Bioinformatics and Biostatistics Unit, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK., Ombrato L; Tumour Host Interaction Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK., Sanz-Moreno V; Sanz-Moreno Lab, Centre for Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK; Randall Division of Cell and Molecular Biophysics, King's College London, New Hunt's House, Guy's Campus, London, SE1 1UL, UK. Electronic address: v.sanz-moreno@qmul.ac.uk., Malanchi I; Tumour Host Interaction Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK. Electronic address: Ilaria.malanchi@crick.ac.uk.
Jazyk: angličtina
Zdroj: Cancer letters [Cancer Lett] 2022 Sep 28; Vol. 544, pp. 215800. Date of Electronic Publication: 2022 Jul 06.
DOI: 10.1016/j.canlet.2022.215800
Abstrakt: Cancer cells thrive when embedded in a fine-tuned cellular and extracellular environment or tumour microenvironment (TME). There is a general understanding of a co-evolution between cancer cells and their surrounding TME, pointing at a functional connection between cancer cells characteristics and the perturbations induced in their surrounding tissue. However, it has never been formally proven whether this functional connection needs to be set from the start or if aggressive cancer cells always dominate their microenvironmental any point in time. This would require a dedicated experimental setting where malignant cells are challenged to grow in a different TME from the one they would naturally create. Here we generated an experimental setting where we transiently perturb the secretory profile of aggressive breast cancer cells without affecting their intrinsic growth ability, which led to the initial establishment of an atypical TME. Interestingly, even if initially tumours are formed, this atypical TME evolves to impair long term in vivo cancer growth. Using a combination of in vivo transcriptomics, protein arrays and in vitro co-cultures, we found that the atypical TME culminates in the infiltration of macrophages with STAT1 high activity. These macrophages show strong anti-tumoural functions which reduce long-term tumour growth, despite lacking canonical M1 markers. Importantly, gene signatures of the mesenchymal compartment of the TME, as well as the anti-tumoural macrophages, show striking prognostic power that correlates with less aggressive human breast cancers.
(Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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