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Palabras clave – provistas por la editorial

well-differentiated papillary mesothelioma; WDPM; malignant mesothelioma; DNA sequencing; mutation; mesothelioma; tumor suppressor; targeted therapy; immunotherapy; biomarkers; proteomics; macrophage-capping protein; fatty acid-binding protein; laminin subunit beta-2; selenium-binding protein 1; carcinogenesis; malignant pleural mesothelioma; asbestos exposure; DNA methylation; lymphocyte-to-monocyte ratio; epigenome-wide analysis; survival analysis; metabolomics; radiotherapy; cancers; inflammation; infiltrating immune cells; prognostic biomarker; predictive biomarker; immune therapy; VATS; extrapleural pneumonectomy; pleurectomy decortication; therapy response; survival; FDG; PET-CT; mesothelium; oxidative stress; redox-sensitive factors; asbestos; carbon nanotubes; protein-protein interactions; systems biology; network analysis; drug repurposing; pleural mesothelioma; gene expression; immunogenicity; sarcomatoid; epithelioid; first line; meta-analysis; systematic review; MPM; lurbinectedin; DNA damage response; histotype; Hippo pathway; NF2; BAP1; CDKN2A; PTCH1; SETD2; MTAP; liquid biopsies; circulating tumor DNA; plasma; cancer-specific mutations; genomics; cancer biomarkers; tumor microenvironment; tumor-associated macrophages; dendritic cells; immunohistochemistry; interaction analysis; pleural effusion; n/a