Functional Interplay Between Collagen Network and Cell Behavior Within Tumor Microenvironment in Colorectal Cancer.

cancer-associated fibroblast collagen colorectal cancer endothelial cell in vitro model tumor cell

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 18 01 2020
accepted: 24 03 2020
entrez: 20 5 2020
pubmed: 20 5 2020
medline: 20 5 2020
Statut: epublish

Résumé

Colorectal cancer is the second most common cancer diagnosed in men and the third most commonly occurring in women worldwide. Interactions between cells and the surrounding extracellular matrix (ECM) are involved in tumor development and progression of many types of cancer. The organization of the ECM molecules provides not only physical scaffoldings and dynamic network into which cells are embedded but also allows the control of many cellular behaviors including proliferation, migration, differentiation, and survival leading to homeostasis and morphogenesis regulation. Modifications of ECM composition and mechanical properties during carcinogenesis are critical for tumor initiation and progression. The core matrisome consists of five classes of macromolecules, which are collagens, laminins, fibronectin, proteoglycans, and hyaluronans. In most tissues, fibrillar collagen is the major component of ECM. Cells embedded into fibrillar collagen interact with it through their surface receptors, such as integrins and discoidin domain receptors (DDRs). On the one hand, cells incorporate signals from ECM that modify their functionalities and behaviors. On the other hand, all cells within tumor environment (cancer cells, cancer-associated fibroblasts, endothelial cells, and immune cells) synthesize and secrete matrix macromolecules under the control of multiple extracellular signals. This cell-ECM dialog participates in a dynamic way in ECM formation and its biophysical and biochemical properties. Here, we will review the functional interplay between cells and collagen network within the tumor microenvironment during colorectal cancer progression.

Identifiants

pubmed: 32426274
doi: 10.3389/fonc.2020.00527
pmc: PMC7204546
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

527

Informations de copyright

Copyright © 2020 Le, Bennasroune, Langlois, Salesse, Boulagnon-Rombi, Morjani, Dedieu and Appert-Collin.

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Auteurs

Cuong Cao Le (CC)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.
Unité BioSpecT, EA7506, Reims, France.

Amar Bennasroune (A)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.

Benoit Langlois (B)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.

Stéphanie Salesse (S)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.

Camille Boulagnon-Rombi (C)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.
Laboratoire de Biopathologie, Centre Hospitalier Universitaire et Faculté de Médecine, Reims, France.

Hamid Morjani (H)

Université de Reims Champagne-Ardenne, Reims, France.
Unité BioSpecT, EA7506, Reims, France.

Stéphane Dedieu (S)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.

Aline Appert-Collin (A)

Université de Reims Champagne-Ardenne, Reims, France.
CNRS UMR 7369, Matrice Extracellulaire et Dynamique Cellulaire, MEDyC, Reims, France.

Classifications MeSH