Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-3-10
pubmed:abstractText
Malignant mesothelioma is a devastating disease that has been associated with loss of Neurofibromatosis type 2 (NF2) and genetic lesions affecting RB and P53 pathways. We introduced similar lesions in the mesothelial lining of the thoracic cavity of mice. Mesothelioma developed at high incidence in Nf2;Ink4a/Arf and Nf2;p53 conditional knockout mice with median survival times of approximately 30 and 20 weeks, respectively. Murine mesothelioma closely mimicked human malignant mesothelioma. Conditional Nf2;Ink4a/Arf mice showed increased pleural invasion compared to conditional Nf2;p53 mice. Interestingly, upon Ink4a loss in the latter mice median survival was significantly reduced and all tumors were highly invasive, suggesting that Ink4a loss substantially contributes to the poor clinical outcome of malignant mesothelioma.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1878-3686
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
261-71
pubmed:dateRevised
2009-5-20
pubmed:meshHeading
pubmed-meshheading:18328429-Adenoviridae, pubmed-meshheading:18328429-Animals, pubmed-meshheading:18328429-Cell Line, Tumor, pubmed-meshheading:18328429-Cell Transformation, Neoplastic, pubmed-meshheading:18328429-Cyclin-Dependent Kinase Inhibitor p16, pubmed-meshheading:18328429-Epithelial Cells, pubmed-meshheading:18328429-Epithelioid Cells, pubmed-meshheading:18328429-Genetic Vectors, pubmed-meshheading:18328429-Genotype, pubmed-meshheading:18328429-Immunohistochemistry, pubmed-meshheading:18328429-Integrases, pubmed-meshheading:18328429-Loss of Heterozygosity, pubmed-meshheading:18328429-Luminescent Measurements, pubmed-meshheading:18328429-Mesothelioma, pubmed-meshheading:18328429-Mice, pubmed-meshheading:18328429-Mice, Knockout, pubmed-meshheading:18328429-Mixed Tumor, Malignant, pubmed-meshheading:18328429-Neoplasm Invasiveness, pubmed-meshheading:18328429-Neoplasms, Experimental, pubmed-meshheading:18328429-Neurofibromatosis 2, pubmed-meshheading:18328429-Phenotype, pubmed-meshheading:18328429-Recombination, Genetic, pubmed-meshheading:18328429-Sarcoma, pubmed-meshheading:18328429-Thoracic Cavity, pubmed-meshheading:18328429-Thoracic Neoplasms, pubmed-meshheading:18328429-Time Factors, pubmed-meshheading:18328429-Tumor Suppressor Protein p53
pubmed:year
2008
pubmed:articleTitle
A conditional mouse model for malignant mesothelioma.
pubmed:affiliation
Department of Molecular Genetics, Cancer Genomics Centre, Centre for Biomedical Genetics, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't