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Genotype and Haplotype Analyses of TP53 Gene in Breast Cancer Patients: Association with Risk and Clinical Outcomes
V. Vymetalkova, P. Soucek, T. Kunicka, K. Jiraskova, V. Brynychova, B. Pardini, V. Novosadova, Z. Polivkova, K. Kubackova, R. Kozevnikovova, M. Ambrus, L. Vodickova, A. Naccarati, P. Vodicka,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT13424
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NT14055
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- MeSH
- Genetic Predisposition to Disease genetics MeSH
- Genotype MeSH
- Genes, p53 genetics MeSH
- Haplotypes genetics MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Breast Neoplasms genetics MeSH
- Risk Factors MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Variations in the TP53 gene have been suggested to play a role in many cancers, including breast. We previously observed an association between TP53 haplotypes based on four polymorphisms (rs17878362, rs1042522, rs12947788, and rs17884306) and the risk of colorectal and pancreatic cancer. Based on these results, in the present study, we have investigated the same polymorphisms and their haplotypes in 705 breast cancer cases and 611 healthy controls in relation to the disease risk, histopathological features of the tumor and clinical outcomes. In comparison to the most common haplotype A1-G-C-G, all the other identified haplotypes were globally associated with a significantly decreased breast cancer risk (P = 0.006). In particular, the A2-G-C-G haplotype was associated with a marked decreased risk of breast cancer when compared with the common haplotype (P = 0.0001). Moreover, rs1042522 in patients carrying the GC genotype and receiving only the anthracycline-based chemotherapy was associated with both overall and disease-free survival (recessive model for overall survival HR = 0.30 95% CI 0.11-0.80, P = 0.02 and for disease-free survival HR = 0.42 95% CI 0.21-0.84, P = 0.01). Present results suggest common genetic features in the susceptibility to breast and gastrointestinal cancers in respect to TP53 variations. In fact, similar haplotype distributions were observed for breast, colorectal, and pancreatic patients in associations with cancer risk. Rs1042522 polymorphism (even after applying the Dunn-Bonferroni correction for multiple testing) appears to be an independent prognostic marker in breast cancer patients.
3rd Faculty of Medicine Charles University Prague Czech Republic
Department of Oncology University Hospital Motol Prague Czech Republic
Department of Oncosurgery MEDICON Prague Czech Republic
Human Genetics Foundation Turin Italy
Institute of Biotechnology Academy of Sciences of the Czech Republic Prague Czech Republic
Institute of Experimental Medicine Academy of Sciences of the Czech Republic Prague Czech Republic
Toxicogenomics Unit National Institute of Public Health Prague Czech Republic
References provided by Crossref.org
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