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Erschienen in: Tumor Biology 4/2014

01.04.2014 | Research Article

Foxp3 promoter polymorphism (rs3761548) in breast cancer progression: a study from India

verfasst von: Parveen Jahan, V. R. Vinish Ramachander, G. Maruthi, S. Nalini, K. Prasanna Latha, T. S. R. Murthy

Erschienen in: Tumor Biology | Ausgabe 4/2014

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Abstract

Breast cancer is the most common female neoplasm that drives the transformation of normal mammary epithelial cells into highly malignant derivatives. Forkhead Box Protein3 (Foxp3), a tumor suppressor/immunomodulatory gene, which controls the function of Treg cells and oncogenes is down regulated in breast cancer. The main aim of the present study is to evaluate the potential influence of Foxp3-3279 C>A polymorphism (rs3761548) and -2383 C>T polymorphism (rs3761549) in 202 breast cancer patients and 130 normal healthy women of Indian origin. The genotypes were determined using ARMS-PCR for rs3761548 and PCR-RFLP method for rs3761549 using specific primers. The results revealed lack of association of these two polymorphisms with breast cancer susceptibility. However, with respect to AA genotype of rs3761548, we found highly significant association with the advanced stage (T3-4) of the tumor (OR = 3.90; 95 % confidence interval (CI) = 1.56–9.70; p = 0.03). Stratified data also revealed an association of homozygous mutant genotype with advanced stage of tumor in premenopausal women (OR = 4.56; 95 % CI = 1.07–19.38; p = 0.04) with disease duration of <6 months (OR = 6.10; 95 % CI = 1.80–20.50; p = 0.002) suggestive of modulating effect of rs3761548 in tumor progression. We conclude that Foxp3 rs37161548 has a potential to be a polymorphic marker for tumor progression in premenopausal breast cancer patients in Indian women.
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Metadaten
Titel
Foxp3 promoter polymorphism (rs3761548) in breast cancer progression: a study from India
verfasst von
Parveen Jahan
V. R. Vinish Ramachander
G. Maruthi
S. Nalini
K. Prasanna Latha
T. S. R. Murthy
Publikationsdatum
01.04.2014
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 4/2014
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-1501-9

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