The case for cancer-associated fibroblasts: essential elements in cancer drug discovery?

Author:

Brewer Gabrielle12ORCID,Fortier Anne-Marie1ORCID,Park Morag12345,Moraes Christopher1367ORCID

Affiliation:

1. Rosalind & Morris Goodman Cancer Research Centre, McGill University, 1160 Avenues des Pins, Montréal, QC, H3A 0G4, Canada

2. Department of Biochemistry, McGill University, 3649 Promenade Sir-William-Osler, Montréal, QC, H3A 0G4, Canada

3. Department of Experimental Medicine, McGill University, 1001 Decarie Boulevard, Montréal, QC, H3A 0G4, Canada

4. Department of Oncology, McGill University, 5100 de Maisonneuve Blvd. West, Montréal, QC, H3A 0G4, Canada

5. Department of Pathology, McGill University, 3775 rue University, Montréal, QC, H3A 0G4, Canada

6. Department of Chemical Engineering, McGill University, 3610 rue University, Montréal, QC, H3A 0G4, Canada

7. Department of Biomedical Engineering, McGill University, 3775 rue University, Montréal, QC, H3A 0G4, Canada

Abstract

Although cancer-associated fibroblasts (CAFs) have gained increased attention for supporting cancer progression, current CAF-targeted therapeutic options are limited and failing in clinical trials. As the largest component of the tumor microenvironment (TME), CAFs alter the biochemical and physical structure of the TME, modulating cancer progression. Here, we review the role of CAFs in altering drug response, modifying the TME mechanics and the current models for studying CAFs. To provide new perspectives, we highlight key considerations of CAF activity and discuss emerging technologies that can better address CAFs; and therefore, increase the likelihood of therapeutic efficacy. We argue that CAFs are crucial components of the cancer drug discovery pipeline and incorporating these cells will improve drug discovery success rates.

Funder

Oncopole

Institute of Cancer Research

Canada Research Chairs

Canadian Cancer Society

Publisher

Future Science Ltd

Subject

General Medicine

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