p53 Haplotype determination in breast cancer Journal Article


Authors: Weston, A.; Pan, C. F.; Ksieski, H. B.; Wallenstein, S.; Berkowitz, G. S.; Tartter, P. I.; Bleiweiss, I. J.; Brower, S. T.; Senie, R. T.; Wolff, M. S.
Article Title: p53 Haplotype determination in breast cancer
Abstract: Inheritance of certain germ line haplotypes consisting of three biallelic polymorphisms of p53 has been proposed as a risk factor fur breast cancer and colorectal cancer [A. Sjalander et al., Carcinogenesis (Lond.), 17: 13131316, 1996, and Carcinogenesis (Lond.), 16: 1461-1464, 1995]. In their studies, pairwise haplotypes of these three polymorphisms were estimated. Extended haplotypes were further projected from the pairwise combinations. To overcome the necessity to estimate pairwise and extended haplotype frequencies, a PCR method has been developed to determine the absolute extended p53 haplotypes in diploid genomes. The method requires allele-specific PCR, confirmed by restriction analysis, and successive amplicon analysis. It has been applied to a nested case-control study of breast cancer (284 subjects; 99 cases and 185 controls; 182 Caucasians, 56 Hispanics, and 46 African-Americans). Evidence is presented that minor variants of the intron 3, codon 72, and intron 6 polymorphisms were moderately elevated in Caucasian breast cancer cases (intron 3, P = 0.03 for genotype and P = 0.01 for allelic frequency; codon 72, P = 0.07 for genotype and P = 0.054 for allelic frequency; and intron 6, P = 0.02 for genotype and P = 0.02 for allele frequency). Accordingly, analysis of haplotype distributions suggested an association of minor p53 haplotypes with breast cancer risk in Caucasians (P = 0.07). The relative allelic frequencies in breast cancer cases compared with controls also differed by age and menopausal status; the 1-2-1 haplotype was overrepresented in postmenopausal cases (P = 0.02) and cases older than 50 years (P = 0.02), whereas the other minor haplotypes (1-1-2 and rare variants) were overrepresented in premenopausal cases (P = 0.003) and cases 50 years of age and younger (P = 0.02). Genotype distributions at each locus and fur all control groups were consistent with Hardy-Weinberg equilibria. Differences in haplotype distribution were associated with ethnicity (Caucasians versus African- Americans and Caucasians versus Hispanics, P < 0.001). The new haplotyping method may be useful in the study of gene-environment interactions.
Keywords: adult; controlled study; aged; middle aged; major clinical study; case-control studies; cancer risk; polymerase chain reaction; breast cancer; logistic models; gene locus; genotype; gene frequency; haplotypes; risk factors; breast neoplasms; protein p53; haplotype; codon; breast carcinogenesis; polymorphism, genetic; diploidy; genes, p53; genetic polymorphism; continental population groups; ethnic groups; humans; human; female; priority journal; article
Journal Title: Cancer Epidemiology Biomarkers and Prevention
Volume: 6
Issue: 2
ISSN: 1055-9965
Publisher: American Association for Cancer Research  
Date Published: 1997-02-01
Start Page: 105
End Page: 112
Language: English
PUBMED: 9037561
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
Citation Impact
MSK Authors
  1. Ruby T. Senie
    15 Senie