TLR2∆22 (-196-174) significantly increases the risk of breast cancer in females carrying proline allele at codon 72 of TP53 gene: a case-control study from four ethnic groups of North Eastern region of India
Autor: | Rup Kumar Phukan, Kanwar Narain, Jishan Ahmed, J Mahanta, Tanvir Kaur, Jason C. Zonunmawia, Gautam Majumdar, Sanjib Kumar Rajguru, Kaustab Mukherjee, Debdutta Mukherjee, K. Rekha Devi, Saia Chenkual |
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Rok vydání: | 2015 |
Předmět: |
Adult
Proline Population India Apoptosis Breast Neoplasms Biology Breast cancer Genetic predisposition medicine Humans Allele education Codon Gene Alleles Genetic Association Studies Aged Sequence Deletion Genetics education.field_of_study Case-control study Promoter General Medicine Middle Aged medicine.disease Immunity Innate Toll-Like Receptor 2 TLR2 Female Tumor Suppressor Protein p53 |
Zdroj: | Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 36(12) |
ISSN: | 1423-0380 |
Popis: | Breast cancer (BC) is the second most common cancer in women. In the North Eastern Region (NER) of India, BC is emerging as an important concern as evidenced by the data available from population and hospital-based cancer registries. Studies on genetic susceptibility to BC are important to understand the increase in the incidence of BC in NER. The present case control study was conducted to investigate the association between tumour suppressor gene TP53 codon 72 polymorphism and innate immune pathway gene TLR2∆22 (-196-174) polymorphism with BC in females of NER of India for the identification of novel biomarker of BC. Four hundred sixty-two histopathologically confirmed BC cases from four states of NER of India, and 770 healthy controls were included by organizing community surveys from the neighbourhood of cases. In our study, no significant association between TP53 codon 72 polymorphisms and the risk of BC was found. However, our study has shown that TP53 codon 72 polymorphism is an important effect modifier. In the present study it was found that females carrying 22 base-pair deletion in the promoter region of their TLR2 gene had two times (AOR= 2.18, 95 % CI 1.13-4.21, p=0.019 in dominant model; AOR= 2.17, 95 % CI 1.09-4.34, p=0.027 in co-dominant model) increased risk of BC whwn they also carry proline allele at codon 72 of their TP53 gene. |
Databáze: | OpenAIRE |
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