Because only a small fraction of asbestos-exposed individuals develop
malignant mesothelioma, and because mesothelioma clustering is observed
in some families, we searched for genetic predisposing factors. We
discovered germline mutations in the gene encoding BRCA1 associated
protein-1 (BAP1) in two families with a high incidence of mesothelioma,
and we observed somatic alterations affecting BAP1 in familial
mesotheliomas, indicating biallelic inactivation. In addition to
mesothelioma, some BAP1 mutation carriers developed uveal melanoma. We
also found germline BAP1 mutations in 2 of 26 sporadic mesotheliomas;
both individuals with mutant BAP1 were previously diagnosed with uveal
melanoma.
We also observed somatic truncating BAP1 mutations and
aberrant BAP1 expression in sporadic mesotheliomas without germline
mutations. These results identify a BAP1-related cancer syndrome that is
characterized by mesothelioma and uveal melanoma. We hypothesize that
other cancers may also be involved and that mesothelioma predominates
upon asbestos exposure. These findings will help to identify individuals
at high risk of mesothelioma who could be targeted for early
intervention.
Keyword Search:
Mutation;
Medical research;
Tumors;
Genetics
Medical research;
Tumors;
Genetics
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