ASSOCIATION OF INTRON 4 VNTR (4A/B) POLYMORPHISM OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE GENE WITH THE INCIDENCE OF BREAST CANCER IN IRAQI WOMEN.

Istikrar M Hade, Zahraa A Ghadhban, Maryam M Abd Ali, Yasir B Qaddoori
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Abstract

Background: The VNTR 4a/b (rs61722009) polymorphism in intron 4 of the NOS3 gene is crucial for various biological processes and has been linked to cancer. Evidence suggests this polymorphism affects NOS3 gene expression and may promote tumor growth in the mammary gland.

Aim: This study aimed to investigate the association between NOS3 4a/b polymorphism and breast cancer (BC) susceptibility in Iraqi women, and to evaluate the potential correlation between these genetic variants and serum cancer antigen 15-3 (CA15-3) levels as a prognostic marker.

Materials and methods: The role of the 4a/b polymorphism was examined using PCR genotyping on dNA extracted from participants, including 50 women with BC and an equal number of controls. The level of CA15-3 was measured in the patients as well.

Results: The homozygous wild-type b/b genotype may confer a protective effect against BC, with a significantly lower frequency in patients (8%) compared to controls (72%) (p < 0.01). Conversely, the heterozygous a/b and homozygous mutant a/ a genotypes were more frequent in patients (50% and 42%, respectively) than in controls (22% and 6%, respectively) (p < 0.01). Notably, the a/a genotype was significantly associated with increased BC risk (OR = 3.08, 95% CI: 1.19-5.47) and predominantly observed in the advanced pT2 stage. Additionally, the mean serum CA15-3 levels were significantly higher in patients with the a/a and a/b genotypes (15.66 U/mL and 22.91 U/mL, respectively) compared to those with the b/b genotype (6.37 U/mL) (p < 0.01).

Conclusion: The differences in genotype and allele frequencies between BC patients and healthy controls, along with the association of polymorphisms with CA15-3 levels, suggest that this genetic marker could serve as a valuable tool for risk assessment as well as prognosis in BC ptients. further investigations with larger and more diverse population samples are needed.

内皮型一氧化氮合酶基因内含子4 VNTR (4a / b)多态性与伊拉克妇女乳腺癌发病率的关系
背景:NOS3基因内含子4中的VNTR 4a/b (rs61722009)多态性对多种生物过程至关重要,并与癌症有关。有证据表明,这种多态性影响NOS3基因的表达,并可能促进乳腺肿瘤的生长。目的:本研究旨在探讨NOS3 4a/b多态性与伊拉克妇女乳腺癌(BC)易感性之间的关系,并评估这些遗传变异与血清癌抗原15-3 (CA15-3)水平作为预后标志物之间的潜在相关性。材料和方法:采用PCR基因分型方法对50名BC女性和同等数量的对照组提取的dNA进行检测4a/b多态性的作用。同时测定患者体内CA15-3水平。结果:纯合子野生型b/b基因型可能对BC具有保护作用,患者(8%)与对照组(72%)相比显著降低(p < 0.01)。相反,杂合子a/b和纯合子突变a/ a基因型在患者中的发生率(分别为50%和42%)高于对照组(分别为22%和6%)(p < 0.01)。值得注意的是,a/a基因型与增加的BC风险显著相关(OR = 3.08, 95% CI: 1.19-5.47),主要见于pT2晚期。a/a和a/b基因型患者血清CA15-3水平(分别为15.66 U/mL和22.91 U/mL)显著高于b/b基因型患者(6.37 U/mL) (p < 0.01)。结论:BC患者与健康对照之间基因型和等位基因频率的差异,以及多态性与CA15-3水平的关联,表明该遗传标记可作为BC患者风险评估和预后的有价值工具。需要对更大、更多样化的人口样本进行进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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