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Julian phillips fox news. Homozygous deletions at chromosome region 9p21 targeting the cdkn2a gene have been reported as a common cytogenetic abnormality in mesothelioma. Homozygous deletion of cdkn2a is frequent in mesothelioma present in 70 of tumors. Melanoma and mesothelioma show a statistically significant co occurrence in the general population.
Mpm is strongly associated with a patients asbestos exposure. In malignant pleural mesothelioma mpm it is one of the most frequently reported genomic alteration. However the status of cdkn2a and the expression of the corresponding protein p16 in relation to mpm patients asbestos exposure.
Fish assay development for the detection of p16cdkn2a deletion in malignant pleural mesothelioma catherine t s chung12 gilda da cunha santos23 david m hwang23 olga ludkovski4 melania pintilie5 jeremy a squire2346 ming sound tsao2346 abstract aims to develop a uorescence in situ hybridisation. Deletion of the cdkn2a locus is centrally involved in the development of several malignancies. Mtap a gene 100 kb telomeric to cdkn2a encodes methylthioadenosine phosphorylase an enzyme essential in the salvage of cellular adenine and methionine and its codeletion with cdkn2a has been reported in other tumors.
Inherited melanoma and mesothelioma predisposition is shown by individual with germline mutations in bap1. Therefore detection of cdkn2a deletion by fluorescence in situ hybridization fish was evaluated as an ancillary test in the cytologic diagnosis of malignant mesothelioma.
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