학술논문

DNA copy number changes in young gastric cancer patients with special reference to chromosome 19.
Document Type
Journal Article
Source
British Journal of Cancer. 6/16/2003, Vol. 88 Issue 12, p1914-1919. 6p.
Subject
*STOMACH cancer
*CHROMOSOMES
*DNA
*PROTEIN analysis
*STOMACH tumors
*NUCLEOTIDE separation
*RESEARCH
*IMMUNOHISTOCHEMISTRY
*NUCLEIC acid hybridization
*RESEARCH methodology
*EVALUATION research
*IMMUNOBLOTTING
*COMPARATIVE studies
*GENOTYPES
*FLUORESCENCE in situ hybridization
Language
ISSN
0007-0920
Abstract
Only a few cytogenetic and genetic studies have been performed in gastric cancer patients in young age groups. In the present study we used the comparative genomic hybridisation (CGH) method to characterise frequent DNA copy number changes in 22 gastric cancer patients of 45 years or younger and three gastric cancer cell lines established from patients younger than 45 years. Analysis of DNA copy number changes revealed frequent DNA copy number increases at chromosomes 17q (52%), 19q (68%) and 20q (64%). To confirm the CGH results and to characterise the amplicon region on the most frequently amplified chromosome, chromosome 19, we carried out fluorescence in situ hybridisation (FISH) analysis and Southern blot analysis. Fluorescence in situ hybridisation with the bacterial artificial chromosome (BAC) clone mapped to 19q12 indicated a copy number increase in all eight tumour specimens studied. Southern blot analysis of six tumour specimens and three tumour cell lines, with five probes mapped to the 19q12-13.2 region, suggested cyclin E to be one of the candidate target genes in the 19q region for gastric cancer tumorigenesis. Cyclin E protein overexpression was verified in tumours with amplification on chromosome 19. Further studies are required to investigate the biological and clinical significance of 19q amplicon and cyclin E upregulation in gastric cancer of young patients. [ABSTRACT FROM AUTHOR]