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Oncogene ; 37(20): 2645-2659, 2018 05.
Article in English | MEDLINE | ID: mdl-29507420

ABSTRACT

Chronic exposure to intraperitoneal asbestos triggered a marked response in the mesothelium well before tumor development. Macrophages, mesothelial precursor cells, cytokines, and growth factors accumulated in the peritoneal lavage. Transcriptome profiling revealed YAP/TAZ activation in inflamed mesothelium with further activation in tumors, paralleled by increased levels of cells with nuclear YAP/TAZ. Arg1 was one of the highest upregulated genes in inflamed tissue and tumor. Inflamed tissue showed increased levels of single-nucleotide variations, with an RNA-editing signature, which were even higher in the tumor samples. Subcutaneous injection of asbestos-treated, but tumor-free mice with syngeneic mesothelioma tumor cells resulted in a significantly higher incidence of tumor growth when compared to naïve mice supporting the role of the environment in tumor progression.


Subject(s)
Asbestos, Crocidolite/adverse effects , Gene Regulatory Networks , Lung Neoplasms/genetics , Mesothelioma/genetics , RNA Editing , Transcriptional Activation , Adaptor Proteins, Signal Transducing , Animals , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Humans , Intracellular Signaling Peptides and Proteins/metabolism , Lung Neoplasms/chemically induced , Lung Neoplasms/metabolism , Macrophage Activation , Mesothelioma/chemically induced , Mesothelioma/metabolism , Mesothelioma, Malignant , Mice , Mutation , Phosphoproteins , Polymorphism, Single Nucleotide , Trans-Activators , Transcription Factors , Transcriptional Coactivator with PDZ-Binding Motif Proteins , YAP-Signaling Proteins
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