Characterisation of the tumour microenvironment and PD-L1 granularity reveals the prognostic value of cancer-associated myofibroblasts in non-invasive bladder cancer

High-risk non-muscle-invasive bladder cancer (NMIBC) presents high recurrence and progression rates. Despite the use of Bacillus Calmette-Guérin gold-standard immunotherapy and the recent irruption of anti-PD-1/PD-L1 drugs, we are missing a comprehensive understanding of the tumor microenvironment (TME) that may help us find biomarkers associated to treatment outcome. Here, we prospectively analyzed TME composition and PD-L1 expression of tumor and non-tumoral tissue biopsies from 73 NMIBC patients and used scRNA-seq, transcriptomic cohorts and tissue micro-array to validate the prognostic value of cell types of interest. Compared to non-tumoral tissue, NMIBC presented microvascular alterations, increased cancer-associated fibroblast (CAF) and myofibroblast (myoCAF) presence, and varied immune cell distribution, such as increased macrophage infiltration. Heterogeneous PD-L1 expression was observed across subsets, with macrophages showing the highest expression levels, but cancer cells as the primary potential anti-PD-L1 binding targets. Unbiased analysis revealed that myoCAF and M2-like macrophages are specifically enriched in high-grade NMIBC tumors. The topological distribution of these two cell types changed as NMIBC progresses, as shown by immunofluorescence. Only myoCAFs were associated with higher rates of progression and recurrence in three independent cohorts (888 total patients), reaching prediction values comparable to transcriptomic classes, which we further validated using tissue micro-array. Our study provides a roadmap to establish the landscape of the NMIBC TME, highlighting myoCAFs as potential prognostic markers.

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Publication Details

Journal
OncoImmunology
Published
2024-12-19
DOI
https://doi.org/10.1080/2162402x.2024.2438291
Citations
10
Primary Topic
Bladder and Urothelial Cancer Treatments
Type
article
Field-Weighted Citation Impact
5.73

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article

Characterisation of the tumour microenvironment and PD-L1 granularity reveals the prognostic value of cancer-associated myofibroblasts in non-invasive bladder cancer

Ester Munera-Maravilla, Marta Dueñas, Daniel Castellano, Carolina Rubio et al.
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OncoImmunology
Bladder and Urothelial Cancer Treatments
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article

Characterisation of the tumour microenvironment and PD-L1 granularity reveals the prognostic value of cancer-associated myofibroblasts in non-invasive bladder cancer

Ester Munera-Maravilla, Marta Dueñas, Daniel Castellano, Carolina Rubio, Cristina Martín‐Arriscado Arroba, Iris Lodewijk, Carmen Gómez del Cañizo, David Lora, Félix Guerrero‐Ramos, Rebeca Sánchez‐Domínguez, Víctor G. Martínez, Marta Rodríguez-Izquierdo, Jaime Martínez de Villarreal, Jesús María Paramio, Cristian Suárez-Cabrera, Sandra P. Nunes, Lucía Morales, Alfredo Rodríguez Antolín, Francisco X. Real, Mercedes Perez Escavy
article en
10 citations

Abstract

High-risk non-muscle-invasive bladder cancer (NMIBC) presents high recurrence and progression rates. Despite the use of Bacillus Calmette-Guérin gold-standard immunotherapy and the recent irruption of anti-PD-1/PD-L1 drugs, we are missing a comprehensive understanding of the tumor microenvironment (TME) that may help us find biomarkers associated to treatment outcome. Here, we prospectively analyzed TME composition and PD-L1 expression of tumor and non-tumoral tissue biopsies from 73 NMIBC patients and used scRNA-seq, transcriptomic cohorts and tissue micro-array to validate the prognostic value of cell types of interest. Compared to non-tumoral tissue, NMIBC presented microvascular alterations, increased cancer-associated fibroblast (CAF) and myofibroblast (myoCAF) presence, and varied immune cell distribution, such as increased macrophage infiltration. Heterogeneous PD-L1 expression was observed across subsets, with macrophages showing the highest expression levels, but cancer cells as the primary potential anti-PD-L1 binding targets. Unbiased analysis revealed that myoCAF and M2-like macrophages are specifically enriched in high-grade NMIBC tumors. The topological distribution of these two cell types changed as NMIBC progresses, as shown by immunofluorescence. Only myoCAFs were associated with higher rates of progression and recurrence in three independent cohorts (888 total patients), reaching prediction values comparable to transcriptomic classes, which we further validated using tissue micro-array. Our study provides a roadmap to establish the landscape of the NMIBC TME, highlighting myoCAFs as potential prognostic markers.

OncoImmunologyVol. 14(1)
Foundation for Biomedical Research (US), Universitat Pompeu Fabra (ES), Universidade do Porto (PT), Research Institute Hospital 12 de Octubre (ES), Spanish National Cancer Research Centre (ES), Hospital Universitario 12 De Octubre (ES), IPO Porto (PT), Centre for Biomedical Network Research on Rare Diseases (ES), Centro de Investigación Biomédica en Red (ES), Research Network (United States) (US), Centro de Investigación Biomédica en Red de Cáncer (ES)
Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, AstraZeneca, Sanofi, F. Hoffmann-La Roche, Comunidad de Madrid, Les Laboratories Pierre Fabre, European Commission, Fundación Científica Asociación Española Contra el Cáncer, Astellas Pharma, Centro de Investigación Biomédica en Red de Cáncer, Ipsen, Fundação para a Ciência e a Tecnologia, Instituto de Salud Carlos III, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas, Agencia Estatal de Investigación
Zero hunger
Openalex Percentile: Top 3%
Bladder and Urothelial Cancer Treatments
5.73
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