1. Identification of a region of homozygous deletion on 8p22โ23.1 in medulloblastoma
- Author
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Ho Keung Ng, Jesse Chung Sean Pang, and Xiao Lu Yin
- Subjects
Adult ,Male ,Cancer Research ,Adolescent ,Tumor suppressor gene ,Allelic Imbalance ,Biology ,medicine.disease_cause ,Polymerase Chain Reaction ,Allelotype Analysis ,Gene mapping ,Genetics ,medicine ,Humans ,Deletion mapping ,Allele ,Child ,Molecular Biology ,Aged ,Medulloblastoma ,Mutation ,Tumor Suppressor Proteins ,GTPase-Activating Proteins ,Homozygote ,Exons ,Middle Aged ,Physical Chromosome Mapping ,medicine.disease ,Child, Preschool ,Nucleic Acid Conformation ,Electrophoresis, Polyacrylamide Gel ,Female ,Gene Deletion ,Chromosomes, Human, Pair 8 ,Microsatellite Repeats ,Comparative genomic hybridization - Abstract
To identify critical tumor suppressor loci that are associated with the development of medulloblastoma, we performed a comprehensive genome-wide allelotype analysis in a series of 12 medulloblastomas. Non-random allelic imbalances were identified on chromosomes 7q (58.3%), 8p (66.7%), 16q (58.3%), 17p (58.3%) and 17q (66.7%). Comparative genomic hybridization analysis confirmed that allelic imbalances on 8p, 16q and 17p were due to loss of genetic materials. Finer deletion mapping in an expanded series of 23 medulloblastomas localized the common deletion region on 8p to an interval of 18.14 cM on 8p22-23.2. We then searched within the region of loss on 8p for loci that might contain homozygous deletion using comparative duplex PCR. An overlapping homozygous deletion region was identified in a 1.8 cM interval on 8p22-23.1, between markers D8S520 and D8S1130, in two medulloblastomas. This region of homozygous deletion also encompasses the 1.4 cM minimal deletion region detected on 8p in ductal carcinoma in situ of breast. In conclusion, we reported for the first time a detailed deletion mapping on 8p in medulloblastoma and have identified a region of homozygous deletion on 8p22-23.1 that is likely to contain a critical tumor suppressor gene involved in the development of medulloblastoma.
- Published
- 2002