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Neuropathol Appl Neurobiol ; 30(3): 304-7, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15175083

ABSTRACT

Choroid plexus carcinomas (CPC) have been shown to carry mutations in the hSNF5/INI1 gene on chromosomal arm 22q11.2. A recent study on choroid plexus papillomas (CPP) and CPC revealed frequent losses of chromosomal portions on the long arm of chromosome 22 (-22q). The region harbouring hSNF5/INI1 was affected in 47% of the CPP and 73% of the CPC, respectively. -22q occurred more frequently in adult than in infantile CPP suggesting different pathogenetic pathways for these tumours. These findings may indicate a potential tumour suppressor gene function of hSNF5/INI1 in a subset of choroid plexus tumours. In order to examine its potential role in the pathogenesis of choroid plexus tumours, we analysed exons 1-9 of hSNF5/INI1 by SSCP analysis in a series of 21 formalin-fixed and paraffin-embedded CPP. No alterations in migratory patterns were detected. These data indicate that somatic point mutations of hSNF5/INI1 do not play a role in the pathogenesis of CPP and that CPP and CPC may arise by two different molecular pathways.


Subject(s)
Choroid Plexus Neoplasms/genetics , DNA-Binding Proteins/genetics , Papilloma, Choroid Plexus/genetics , Point Mutation/genetics , Chromosomal Proteins, Non-Histone , Chromosomes, Human, Pair 22/genetics , DNA Mutational Analysis , Exons/genetics , Humans , Polymorphism, Single-Stranded Conformational , SMARCB1 Protein , Tissue Fixation , Transcription Factors
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