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FOXP3 Genetic Variation at Position -2383 C/T (rs3761549) in Patients with Breast Cancer | ||
Middle East Journal of Cancer | ||
مقاله 3، دوره 10، شماره 4 - شماره پیاپی 40، دی 2019، صفحه 299-304 اصل مقاله (582.89 K) | ||
نوع مقاله: Original Article(s) | ||
شناسه دیجیتال (DOI): 10.30476/mejc.2019.78638. | ||
نویسندگان | ||
Zahra Shiri1؛ Reza Mansouri1، 2؛ Mohammad Reza Haghshenas3؛ Abdolrasoul Talei4، 5؛ Nasrollah Erfani* 6 | ||
1Department of Immunology, Faculty of Medicine, International Branch of Shahid Sadoughi University of Medical Sciences, Yazd, Iran | ||
2Hematology and Oncology Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran | ||
3Shiraz Institute for Cancer Research, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran | ||
4Breast Disease Research Center, Shiraz University of Medical Sciences, Shiraz, Iran | ||
5Department of Surgery, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran | ||
6Department of Immunology and Shiraz Institute for Cancer Research, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran | ||
چکیده | ||
Background:We investigated the possibility of an association between the C-2383T polymorphism (rs3761549) in the promoter region of the FOXP3 gene with breast cancer. Methods: The study groups consisted of 250 women diagnosed with breast cancer (case group) and 250 healthy women (control group). Polymerase chain reactionrestriction fragment length polymorphism was performed for genotyping. Results: Breast cancer cases had a C allele frequency of 455 (91%) and T allele frequency of 45 (9%). The control group had a C allele frequency of 468 (93.6%) and 32 (6.4%) for the T allele. The CC genotype was present in 206 (82.4%) patients, 43 (17.2%) patients had the CT genotype, and the TT genotype was observed in 1 (0.4%) patient. In the control group, 219 (87.6%) had the CC genotype, whereas 30 (12%) had the CT genotype, and 1 (0.4%) had the TT genotype. Statistical analysis revealed no significant differences in the distribution of alleles and genotypes between patients and controls (P>0.05). There was no significant association between genotype distribution and patients' clinicopathological factors. Conclusion: Our results do not support an association between the FOXP3 -2383 C/T polymorphism and breast cancer in a population from southern Iran. | ||
کلیدواژهها | ||
Breast cancer؛ FOXP3 gene؛ Single nucleotide polymorphism؛ PCR-RFLP | ||
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