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Lack of any Association of the CTLA-4 +49 G/A Polymorphism with Breast Cancer Risk in a North Indian Population
- Source :
- Asian Pacific Journal of Cancer Prevention. 15:2035-2038
- Publication Year :
- 2014
- Publisher :
- Asian Pacific Organization for Cancer Prevention, 2014.
-
Abstract
- Cytotoxic T-lymphocyte antigen 4 (CTLA-4) is an important protein involved in the regulation of the immune system. The +49 G/A polymorphism is the only genetic variation in the CTLA-4 gene that causes an amino acid change in the resulting protein. It is therefore the most extensively studied polymorphism among all CTLA-4 genetic variants and contributions to increasing the likelihood of developing cancer are well known in various populations, especially Asians. However, there have hiterto been no data with respect to the effect of this polymorphism on breast cancer susceptibility in our North Indian population. We therefore assayed genomic DNA of 250 breast cancer subjects and an equal number of age-, sex- and ethnicity-matched healthy controls for the CTLA-4 +49 G/A polymorphism but no significant differences in either the gene or allele frequency were found. Thus the CTLA-4 +49 G/A polymorphism may be associated with breast cancer in other Asians, but it appears to have no such effect in North Indians. The study also highlights the importance of conducting genetic association studies in different ethnic populations.
- Subjects :
- Risk
Cancer Research
Genotype
Epidemiology
Breast Neoplasms
Single-nucleotide polymorphism
Biology
Polymorphism, Single Nucleotide
Breast cancer
Asian People
Gene Frequency
Genetic variation
medicine
Humans
CTLA-4 Antigen
Genetic Predisposition to Disease
Gene
Allele frequency
Genetic association
Genetics
Public Health, Environmental and Occupational Health
Case-control study
medicine.disease
Oncology
Case-Control Studies
Immunology
Female
Subjects
Details
- ISSN :
- 15137368
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Asian Pacific Journal of Cancer Prevention
- Accession number :
- edsair.doi.dedup.....77fe6ae2ec0b2845e1e33b36c69bd0a2