Grupo de Inmunidad del Cáncer

Inicio | Investigación e innovación | Programas Científicos | Programa de Oncología Molecular | Grupo de Inmunidad del Cáncer

María Casanova

Investigadores Científicos

  • Alba de Juan

Becarios Post-doctorales

  • Raquel González-Novo
  • Ana Mantrana
  • Sarai Martínez

Becarios Pre-Doctorales

  • Eduardo Garvín
  • Jan Hochstadt
  • Mariola Munárriz

Técnicos de Laboratorio

  • David Cáceres
  • Mónica Gómez
  • María Nogales

Myeloid cells are abundant in solid tumours. While their heterogeneity has been widely described, efficient ways of manipulating these cells are scarce. My laboratory focuses on the identification and therapeutic targeting of myeloid checkpoint programmes in cancer. By studying the microenvironment in which lung, ovarian, and breast cancer emerge, we examine how macrophages crosstalk with the stroma and how they modulate their malignant conversion into cancer-associated fibroblasts. As metastasis is the major cause of death in breast cancer, we explore the mechanisms by which neutrophils exacerbate metastasis malignancy. Lastly, understanding how tissue physiology is perturbed in cancer is key to investigating novel ways to modulate anti-tumour immunity: we do this by exploring the circadian biology of immune responses, interrogating how our diet modifies the lipid metabolism of macrophages, and mining the dysfunctional properties of bone marrow-derived haematopoiesis.

Publicaciones

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  • Ortega-Molina A, Lebrero-Fernández C, Sanz A, Calvo-Rubio M, Deleyto-Seldas N, de Prado-Rivas L, Plata-Gómez AB, Fernández-Florido E, González-García P, Vivas-García Y, Sánchez García E, Graña-Castro O, Price NL, Aroca-Crevillén A, Caleiras E, Monleón D, Borrás C, Casanova-Acebes M, de Cabo R, Efeyan A. (2024). A mild increase in nutrient signaling to mTORC1 in mice leads to parenchymal damage, myeloid inflammation and shortened lifespan. Nature Aging 4, 1102-1120. Publicación CNIO. Open Access Open Access
  • Park MD, Reyes-Torres I, LeBerichel J, Hamon P, LaMarche NM, Hegde S, Belabed M, Troncoso L, Grout JA, Magen A, Humblin E, Nair A, Molgora M, Hou J, Newman JH, Farkas AM, Leader AM, Dawson T, D'Souza D, Hamel S, Sanchez-Paulete AR, Maier B, Bhardwaj N, Martin JC, Kamphorst AO, Kenigsberg E, Casanova-Acebes M, Horowitz A, Brown BD, De Andrade LF, Colonna M, Marron TU, Merad M (2023). TREM2 macrophages drive NK cell paucity and dysfunction in lung cancer. Nat Immunol 24, 792-801. Publicación CNIO. Open Access Open Access
  • Grout JA, Sirven P, Leader AM, Maskey S, Hector E, Puisieux I, Steffan F, Cheng E, Tung N, Maurin M, Vaineau R, Karpf L, Plaud M, Begue AL, Ganesh K, Mesple J, Casanova-Acebes M, Tabachnikova A, Keerthivasan S, Lansky A, Le Berichel J, Walker L, Rahman AH, Gnjatic S, Girard N, Lefevre M, Damotte D, Adam J, Martin JC, Wolf A, Flores RM, Beasley MB, Pradhan R, Muller S, Marron TU, Turley SJ, Merad M, Kenigsberg E, Salmon H (2022). Spatial Positioning and Matrix Programs of Cancer-Associated Fibroblasts Promote T-cell Exclusion in Human Lung Tumors. Cancer Discovery 12, 2606-2625. Publicación CNIO. Open Access Open Access
  • Casanova-Acebes, M., Dalla, E., Leader, A.M, LeBerichel J, Nikolic J, Morales BM , Brown M, Chang C, Troncoso L, Chen ST, Sastre-Perona A, Park M, Tabachnikova A, Dhainaut M, Hamon P, Maier B, Sawai CM, Agulló-Pascual E, Chober M, Brown BD, Reizis B, Marron T, Kenigsberg E, Moussion C, Benaroch, Aguirre-Ghiso JA, Merad M (2021). Tissue-resident macrophages provide a pro-tumorigenic niche to early NSCLC cells. Nature 595, 578-584. Publicación en otras instituciones.
  • Hidalgo A , Casanova-Acebes M (2021). Dimensions of neutrophil life and fate. Semin Immunol (in press). Publicación CNIO.
  • Casanova-Acebes M, Menéndez-Gutiérrez MP, Porcuna J, Álvarez-Errico D, Lavin Y, García A, Kobayashi S, Le Berichel J, Núñez V, Were F, Jiménez-Carretero D, Sánchez-Cabo F, Merad M, Ricote M (2020). RXRs control serous macrophage neonatal expansion and identity and contribute to ovarian cancer progression.. Nat Commun 11, 1655. Publicación en otras instituciones.

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