Korean J Pathol.
1999 Jun;33(6):422-433.
DNA Sequencing of p53 Gene Mutation in Colorectal Carcinomas
- Affiliations
-
- 1Department of Pathology, Yeungnam University College of Medicine, Taegu 705-717, Korea.
Abstract
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Mutations in the p53 gene occur during the development of colorectal carcinomas,
and play an important role in the conversion of adenoma into carcinoma. To detect the
p53 gene mutation and its pattern of expression in colorectal carcinomas, polymerase
chain reaction for exons 5, 6, 7, and 8, recombinant gene cloning, and automated DNA
sequencing were performed with 30 fresh colorectal carcinomas. Each tissue was also
analyzed by immunohistochemical staining for p53 protein. p53 protein was detected in 25
of 30 (83.3%) colorectal carcinomas by immunohistochemical study. p53 mutation was
detected in 4 of 30 (13.3%) colorectal carcinomas. The distribution of these mutations
among these exons investigated was as follows: Three mutations in exon 5 (66.7%) and
1 mutation in exon 7 (33.3%). One case with mutation in exon 5 had mutations at three
different codons. Mutations in exon 5 were found at codon 153 (GGG to AGG: Gly to
Arg), 170 (TGC to GGC: Cys to Gly), 186 (CTA to TTA: silent mutation), 158 (GCG to
ACG: Ala to Thr), and 176 (ACG to ATG: Thr to Met). Mutation in exon 7 was found
at codon 248 (AGG to AGA: silent mutation). Four of them were missense mutations.
Two of 6 mutations were silent mutations. Five transition mutations and 1 transversion
mutation were also detected. All cases with mutations by automated DNA sequencing
showed positive p53 protein immunohistochemical stainining. In conclusion, p53 gene
mutation was detected in 4 of 30 (13.3%) colorectal carcinomas, located in codon 153,
158, 170, 176, and 186 of exon 5 and codon 248 of exon 7. Further studies are needed to
evaluate the significance of the codon 153 mutation which was not recognized in other
studies on colorectal carcinomas.