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功能性 4 碱基对插入/缺失 ATTG 多态性位于 NF-KB1 启动子区域,降低 BC 的发病风险。

The functional 4-bp insertion/deletion ATTG polymorphism in the promoter region of NF-KB1 reduces the risk of BC.

机构信息

Genetic of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.

Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

Cancer Biomark. 2016;16(1):109-15. doi: 10.3233/CBM-150546.

Abstract

Nuclear factor kappaB (NF-kB) plays a key role in mammary gland development and breast cancer (BC) progression. A functional -94 insertion/deletion ATTG polymorphism (rs28362491) in the promoter of the NFKB1 gene was reported to affect NF-KB1 expression and confer susceptibility to different types of cancer. The current study aimed to assess the association of NFKB1 -94 insertion/deletion ATTG promoter polymorphism and BC risk in an Iranian population. A total of 439 subjects including on 236 BC patients and 203 healthy women were recruited. The NF-KB1 -94ins/del ATTG polymorphism was genotyped by Allele-Specific polymerase chain reaction (AS-PCR) method. Our results demonstrated that the NF-KB1 -94ins/del ATTG polymorphism was associated with a reduced risk of BC in Codominant (Ins/Ins vs. Del/Del: OR = 0.33, 95%CI = 0.17-0.64; P= 0.001), dominant (Ins/Ins vs. Ins/Del+Del/Del: OR = 0.64, 95%CI = 0.42-0.97; P= 0.027) and recessive (Ins/Del+Del/Del vs. Del/Del: OR = 0.40, 95%CI = 0.21-0.75; P= 0.002) tested inheritance models. Additionally, the Del allele of NF-KB1 -94ins/del ATTG variation with a higher prevalence in the control group compared to the BC patients (43.3% vs. 33.5%) was associated with a decreased risk of BC (OR = 0.66, 95%CI = 0.50-0.86, P= 0.003). In conclusion, our findings for the first time, suggest that the NF-KB1 -94ins/del Del allele and Del/Del genotype were associated with a reduced risk of BC which may contribute as protective factors against BC.

摘要

核因子 kappaB(NF-kB)在乳腺发育和乳腺癌(BC)进展中发挥关键作用。据报道,NFKB1 基因启动子中的功能性 -94 插入/缺失 ATTG 多态性(rs28362491)会影响 NF-KB1 表达并易患不同类型的癌症。本研究旨在评估伊朗人群中 NFKB1-94 插入/缺失 ATTG 启动子多态性与 BC 风险的关联。共招募了 439 名受试者,包括 236 名 BC 患者和 203 名健康女性。NF-KB1-94ins/del ATTG 多态性通过等位基因特异性聚合酶链反应(AS-PCR)方法进行基因分型。我们的结果表明,NF-KB1-94ins/del ATTG 多态性与 BC 风险降低相关,在共显性(Ins/Ins 与 Del/Del:OR = 0.33,95%CI = 0.17-0.64;P = 0.001)、显性(Ins/Ins 与 Ins/Del+Del/Del:OR = 0.64,95%CI = 0.42-0.97;P = 0.027)和隐性(Ins/Del+Del/Del 与 Del/Del:OR = 0.40,95%CI = 0.21-0.75;P = 0.002)遗传模型中均如此。此外,与 BC 患者相比,NF-KB1-94ins/del ATTG 变异的 Del 等位基因在对照组中更为常见(43.3% 比 33.5%),与 BC 风险降低相关(OR = 0.66,95%CI = 0.50-0.86,P = 0.003)。总之,我们的研究结果首次表明,NF-KB1-94ins/del Del 等位基因和 Del/Del 基因型与 BC 风险降低相关,这可能是 BC 的保护因素。

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