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SPARC in cancer-associated fibroblasts is an independent poor prognostic factor in non-metastatic triple-negative breast cancer and exhibits pro-tumor activity.
Alcaraz, Lindsay B; Mallavialle, Aude; Mollevi, Caroline; Boissière-Michot, Florence; Mansouri, Hanane; Simony-Lafontaine, Joelle; Laurent-Matha, Valérie; Chardès, Thierry; Jacot, William; Turtoi, Andrei; Roger, Pascal; Guiu, Séverine; Liaudet-Coopman, Emmanuelle.
Afiliación
  • Alcaraz LB; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Mallavialle A; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Mollevi C; Biometry Unit, ICM, University of Montpellier, Montpellier, France.
  • Boissière-Michot F; Desbrest Institute of Epidemiology and Public Health, University of Montpellier, INSERM, Montpellier, France.
  • Mansouri H; Translational Research Unit, ICM, Montpellier, France.
  • Simony-Lafontaine J; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Laurent-Matha V; RHEM, IRCM, Montpellier, France.
  • Chardès T; Translational Research Unit, ICM, Montpellier, France.
  • Jacot W; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Turtoi A; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Roger P; IRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
  • Guiu S; Translational Research Unit, ICM, Montpellier, France.
  • Liaudet-Coopman E; Department of Medical Oncology, ICM, Montpellier, France.
Int J Cancer ; 152(6): 1243-1258, 2023 03 15.
Article en En | MEDLINE | ID: mdl-36346290
Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype and lacks specific targeted therapeutic agents. The current mechanistic evidence from cell-based studies suggests that the matricellular protein SPARC has a tumor-promoting role in TNBC; however, data on the clinical relevance of SPARC expression/secretion by tumor and stromal cells in TNBC are limited. Here, we analyzed by immunohistochemistry the prognostic value of tumor and stromal cell SPARC expression in 148 patients with non-metastatic TNBC and long follow-up (median: 5.4 years). We also quantified PD-L1 and PD-1 expression. We detected SPARC expression in tumor cells (42.4%), cancer-associated fibroblasts (CAFs; 88.1%), tumor-associated macrophages (77.1%), endothelial cells (75.2%) and tumor-infiltrating lymphocytes (9.8%). Recurrence-free survival was significantly lower in patients with SPARC-expressing CAFs. Multivariate analysis showed that SPARC expression in CAFs was an independent prognostic factor. We also detected tumor and stromal cell SPARC expression in TNBC cytosols, and in patient-derived xenografts and cell lines. Furthermore, we analyzed publicly available single-cell mRNA sequencing data and found that in TNBC, SPARC is expressed by different CAF subpopulations, including myofibroblasts and inflammatory fibroblasts that are involved in tumor-related processes. We then showed that fibroblast-secreted SPARC had a tumor-promoting role by inhibiting TNBC cell adhesion and stimulating their motility and invasiveness. Overall, our study demonstrates that SPARC expression in CAFs is an independent prognostic marker of poor outcome in TNBC. Patients with SPARC-expressing CAFs could be eligible for anti-SPARC targeted therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama Triple Negativas / Fibroblastos Asociados al Cáncer / Antineoplásicos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Cancer Año: 2023 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama Triple Negativas / Fibroblastos Asociados al Cáncer / Antineoplásicos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Cancer Año: 2023 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos