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PMID: 8240361 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

p53 gene mutations in pontine gliomas of juvenile onset.

Biochemical and biophysical research communications ·Vol. 196 ·No. 2 ·1993-10-29 ·Pages 851-7

Zhang S, Feng X, Koga H, Ichikawa T, Abe S, Kumanishi T

Abstract

Using polymerase chain reaction-single strand polymorphism(PCR-SSCP) and nucleotide analyses, p53 gene mutation was examined in 13 pontine gliomas many of which were of juvenile onset. A total of 15 mutations were detected in 8 cases, of which 5 revealed multiple or tandem mutations. The mutations included 6 G:C-A:T and 4 A:T-G:C transitions and 4 G:C-T:A and 1 A:T-T:A transversions. There was only 1 transition at the CpG site. Normal tissues of the same patients revealed no mutation, suggesting that these mutations were somatic, but not of germ line, in nature. The pattern of mutation characterized by frequent multiple or tandem occurrence, predominancy of transition at non-CpG sites and relatively frequent transversions suggested that pontine glioma might be related with some mutagenic or carcinogenic agents.

Related Genes
p53
MeSH Terms
Amino Acid Sequence Astrocytoma/genetics Base Sequence Brain/metabolism Brain Neoplasms/genetics,metabolism,radiotherapy Child Child, Preschool Codon/genetics DNA Primers Exons Female Genes, p53 Glioma/genetics,metabolism,radiotherapy Humans Male Point Mutation Polymerase Chain Reaction Pons Tumor Suppressor Protein p53/genetics
Chemicals
Codon DNA Primers Tumor Suppressor Protein p53
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zhang S
Department of Neuropathology, Niigata University, Japan.
Feng X
Koga H
Ichikawa T
Abe S
Kumanishi T
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1993-10-29
Pages
851-7
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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