Fibroblast heterogeneity in solid tumors: From single cell analysis to whole-body imaging.


Journal

Seminars in cancer biology
ISSN: 1096-3650
Titre abrégé: Semin Cancer Biol
Pays: England
ID NLM: 9010218

Informations de publication

Date de publication:
11 2022
Historique:
received: 09 01 2022
revised: 09 03 2022
accepted: 24 04 2022
pubmed: 1 5 2022
medline: 23 11 2022
entrez: 30 4 2022
Statut: ppublish

Résumé

Cancer-Associated Fibroblasts (CAFs) represent the most prominent component of the tumor microenvironment (TME). Recent studies demonstrated that CAF are heterogeneous and composed of different subpopulations exerting distinct functions in cancer. CAF populations differentially modulate various aspects of tumor growth, including cancer cell proliferation, extra-cellular matrix remodeling, metastatic dissemination, immunosuppression and resistance to treatment. Among other markers, the Fibroblast Activation Protein (FAP) led to the identification of a specific CAF subpopulation involved in metastatic spread and immunosuppression. Expression of FAP at the surface of CAF is detected in many different cancer types of poor prognosis. Thus, FAP recently appears as an appealing target for therapeutic and molecular imaging applications. In that context,

Identifiants

pubmed: 35489628
pii: S1044-579X(22)00102-X
doi: 10.1016/j.semcancer.2022.04.008
pii:
doi:

Substances chimiques

Gelatinases EC 3.4.24.-
Serine Endopeptidases EC 3.4.21.-
Membrane Proteins 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

262-272

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest F.M.-G. received research support from Innate-Pharma, Roche and Bristol-Myers-Squibb (BMS). A.P. declares no potential conflict of interest. F-C.B. received research support from Roche. I.B. receives research support from Siemens Healthineers, GE Healthcare and Dosisoft.

Auteurs

Agathe Peltier (A)

Institut Curie, Stress and Cancer Laboratory, Equipe labélisée par la Ligue Nationale contre le Cancer, PSL Research University, 26, rue d'Ulm, F-75248 Paris, France; Inserm, U830, 26, rue d'Ulm, Paris, F-75005 France.

Romain-David Seban (RD)

Nuclear Medicine Department, Institut Curie Hospital Group, 35 rue Dailly, 92210 Saint-Cloud, France; Laboratoire d'Imagerie Translationnelle en Oncologie (LITO), U1288 Inserm, Institut Curie, Orsay, France.

Irène Buvat (I)

Laboratoire d'Imagerie Translationnelle en Oncologie (LITO), U1288 Inserm, Institut Curie, Orsay, France. Electronic address: irene.buvat@curie.fr.

François-Clément Bidard (FC)

Department of Medical Oncology, Inserm CIC-BT 1428, Institut Curie, UVSQ/Paris Saclay University, Saint-Cloud, France. Electronic address: francois-clement.bidard@curie.fr.

Fatima Mechta-Grigoriou (F)

Institut Curie, Stress and Cancer Laboratory, Equipe labélisée par la Ligue Nationale contre le Cancer, PSL Research University, 26, rue d'Ulm, F-75248 Paris, France; Inserm, U830, 26, rue d'Ulm, Paris, F-75005 France. Electronic address: fatima.mechta-grigoriou@curie.fr.

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Classifications MeSH