MUC1 Drives the Progression and Chemoresistance of Clear Cell Renal Carcinomas

Author:

Bourdon Emma1,Swierczewski Thomas1ORCID,Goujon Marine1,Boukrout Nihad1,Fellah Sandy1,Van der Hauwaert Cynthia1ORCID,Larrue Romain12,Lefebvre Bruno3ORCID,Van Seuningen Isabelle1ORCID,Cauffiez Christelle1ORCID,Pottier Nicolas13,Perrais Michaël1

Affiliation:

1. Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, UMR9020-U1277–CANTHER–Cancer Heterogeneity Plasticity and Resistance to Therapies, F-59000 Lille, France

2. CHU Lille, Service de Toxicologie et Génopathies, F-59000 Lille, France

3. Univ. Lille, CNRS, Inserm, CHU Lille, UMR-S1172, Neuroscience & Cognition, Alzheimer & Tauopathies, F-59000 Lille, France

Abstract

While the transmembrane glycoprotein mucin 1 (MUC1) is clustered at the apical borders of normal epithelial cells, with transformation and loss of polarity, MUC1 is found at high levels in the cytosol and is uniformly distributed over the entire surface of carcinoma cells, where it can promote tumor progression and adversely affects the response to therapy. Clear cell renal cell carcinoma (ccRCC), the main histotype of kidney cancer, is typically highly resistant to conventional and targeted therapies for reasons that remain largely unknown. In this context, we investigated whether MUC1 also plays a pivotal role in the cellular and molecular events driving ccRCC progression and chemoresistance. We showed, using loss- and gain-of-function approaches in ccRCC-derived cell lines, that MUC1 not only influences tumor progression but also induces a multi-drug-resistant profile reminiscent of the activation of ABC drug efflux transporters. Overall, our results suggest that targeting MUC1 may represent a novel therapeutic approach to limit ccRCC progression and improve drug sensitivity.

Funder

la Ligue Nationale Contre le Cancer

Contrat de Plan Etat Région CPER Cancer

Lille University

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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