苏丹乳腺癌患者VDR基因Taq1 rs: 731236 SNP与危险因素的相关性研究

Amira S. Khalafalla, Abuagla M. Dafalla, Y. Mohammed, A. Abakar, M. Adil, G. Modawe
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引用次数: 0

摘要

简介:乳腺癌是全球以及苏丹妇女中最常见的癌症,它已上升为妇女死亡的第二大常见原因。维生素D受体(VDR)是一种依赖配体的转录因子。维生素d配体dvdr通过诱导细胞周期阻滞、衰老、分化和死亡,在多种肿瘤类型中具有抗增殖特性。VDR TaqI多态性的作用目前尚不清楚。然而,研究表明这些多态性可能会影响信使RNA (mRNA)的稳定性。方法:本病例对照198例,其中97例为乳腺癌患者,另设101例为对照组。通过问卷调查收集数据。取静脉血2ml, -20℃保存至提取DNA。采用苯酚-氯仿法提取DNA。设计合适的引物和PCR条件后,采用CTPP-PCR对VDR TaqI进行检测和分型。然后使用SPSS软件(版本21)和SNPStats在线工具对数据进行统计分析。结果:本研究报道的TaqI SNP的三种基因型(CC、TC、TT)在病例和对照组中分布均匀,因此根据本研究结果,该SNP与乳腺癌风险的相关性无统计学意义(p值0.650)(OR(95%CI) 1.39(0.64-3.00)、1.00(0.54-1.87)、1.00)。结论:本研究未发现TaqI多态性与乳腺癌危险因素相关
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between Taq1 rs: 731236 SNP of VDR gene and risk factor among Sudanese patients with breast cancer
Introduction: Breast cancer is the most frequent cancer in women globally as well asSudan, it has risen to become the second commonest cause of death in women.Vitamin D receptor (VDR) is a ligand-dependent transcription factor. Vitamin D-ligandedVDR, has antiproliferative properties in a variety of tumor types by inducing cell cycle arrest, senescence, differentiation, and death. The role of VDR TaqI polymorphism is currently unknown. However, studies suggest that these polymorphisms may affect messenger RNA (mRNA) stability. Methods:This case control 198 participants, (97) breast cancer patients and another 101control group.Data wascollectedby a questionnaire. 2 ml of venous blood was collected and stored at -20 till DNA extraction. Phenol chloroform method was used for DNA extraction. VDR TaqI was examined and genotyped using CTPP-PCR after designing of suitable primers and PCR condition. Then data was analyzed statistically using the SPSS program (version 21) and the SNPStats online tool. Results:the three genotypes reported in this study for TaqI SNP (CC, TC, and TT) were evenly distributed throughout cases and controls, so according to this findings there is no statistically significant association of this SNP with breast cancer risk (p. value 0.650) (OR(95%CI) 1.39 (0.64-3.00), 1.00 (0.54-1.87), 1.00). Conclusions:This study found no association of TaqI polymorphism and breast cancer riskfactors
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