1. Chromosome 10 and 17 deletions and p53 gene mutations in Thai patients with astrocytomas.
- Author
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Put-Ti-Noi S, Petmitr S, Chanyavanich V, Sangruji T, Theerapuncharoen V, Hayashi K, and Thangnipon W
- Subjects
- Adult, Aged, Astrocytoma genetics, Base Sequence, DNA Mutational Analysis, DNA, Neoplasm chemistry, DNA, Neoplasm genetics, Exons genetics, Female, Glioblastoma genetics, Glioblastoma pathology, Humans, Loss of Heterozygosity, Male, Microsatellite Repeats, Middle Aged, Polymorphism, Single-Stranded Conformational, Thailand, Astrocytoma pathology, Chromosome Deletion, Chromosomes, Human, Pair 10 genetics, Chromosomes, Human, Pair 17 genetics, Mutation, Tumor Suppressor Protein p53 genetics
- Abstract
The tumor suppressor gene locus is known to be partly responsible for the tumorigenesis of sporadic gliomas, but the genetic events that drive the neoplastic process of this tumor remain largely unknown. We correlated the results of loss of heterozygosity (LOH) analysis on chromosomes 10 and 17 and a point mutation analysis of a tumor suppressor gene, p53, in 21 patients with astrocytomas at different stages. LOH was determined in tumor and leukocyte DNAs of primary human central nervous system tumors. The incidence rate of brain tumors corresponded to every p53-coding exon for single-strand conformation polymorphisms (SSCP) and the mutations were confirmed by sequencing. p53 mutations were found in 2 of 10 glioblastomas (20%) and in 1 of 8 low-grade astrocytomas (12.5%). Similarly, LOH on chromosome 10 was also found in 2 of 10 glioblastomas (20%) and 1 of 8 low-grade astocytomas (12.5%). Neither of the p53 mutations nor LOH on chromosome 10 was observed together in the tumor types analyzed. Interestingly, the p53 mutations were found in 29% of patients with LOH on chromosome 17. The fact that p53 mutation and LOH on chromosome 17 were found together only in glioblastomas, suggested that these genetic changes may accumulate during astrocytoma progression.
- Published
- 2004