Study of the potential association of the BCHE rs1803274 genetic polymorphism and serum level of its protein with breast cancer

IF 0.8 Q4 GENETICS & HEREDITY Meta Gene Pub Date : 2021-09-01 DOI:10.1016/j.mgene.2021.100913
Mona S. Habieb , Nesreen G. Elhelbawy , Alshimaa M. Alhanafy , Mohammad G. Elhelbawy , Ahmed S. Alkelany , Amany M. Wahb
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引用次数: 2

Abstract

Background

Genetic-based individual differences remain a promising area for studying cancer susceptibility. BCHE gene encodes the butyrylcholinesterase (BChE) enzyme, which has been linked to inflammation and tumor genesis. The commonest missense mutation of BCHE gene is the rs1803274 G/A polymorphism. We aimed to analyze BCHE rs1803274 gene polymorphism in terms of distribution among breast cancer patients, its effect on enzyme activity and its correlation with clinic pathological parameters.

Methods

160 breast cancer female patients matched by age with 120 female healthy controls were recruited. CA 15–3 and CEA were measured by ELISA. BChE activity was measured by spectrophotometry. BCHE rs1803274 polymorphism was analyzed by real time- PCR.

Results

Significant higher prevalence of GA genotype and A allele were observed in patients [P < 0.001, OR (95% CI); 3.12 (1.67–5.85), P < 0.001, OR (95% CI); 2.86 (1.68–4.87) respectively]. This significance was observed under the dominant mode of inheritance (P < 0.001, OR (95% CI); 3.22 (1.78–5.85). GA + AA patients showed significant association with tumor grade, stage, and metastasis (P < 0.001). GA + AA patients exhibited significantly lower BChE activity compared to GG patients (3648.5 (2968–4332) mU/ml and 7128.5 (6332–8341) mU/ml respectively, P < 0.001).

Conclusions

Higher frequency of the A-variant of BCHE rs1803274 and the associated low activity of BChE in breast cancer patients could represent susceptibility elements for development of breast cancer. Moreover, the rs1803274 is linked to some tumor features, which could be a proof of its prognostic value.

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BCHE rs1803274基因多态性及其血清蛋白水平与乳腺癌的潜在关联研究
基于遗传的个体差异仍然是研究癌症易感性的一个有前途的领域。BCHE基因编码与炎症和肿瘤发生有关的丁基胆碱酯酶(BCHE)。BCHE基因最常见的错义突变是rs1803274 G/A多态性。我们旨在分析BCHE rs1803274基因多态性在乳腺癌患者中的分布、对酶活性的影响及其与临床病理参数的相关性。方法选取160例年龄匹配的女性乳腺癌患者和120例健康对照。ELISA法检测ca15 - 3和CEA。用分光光度法测定BChE活性。实时荧光定量PCR检测BCHE rs1803274基因多态性。结果GA基因型和A等位基因在患者中的患病率明显高于对照组[P <0.001,或(95% ci);3.12 (1.67-5.85), P <0.001,或(95% ci);分别为2.86(1.68-4.87)。这种显著性在显性遗传模式下被观察到(P <0.001,或(95% ci);3.22(1.78 - -5.85)。GA + AA患者与肿瘤分级、分期和转移有显著相关性(P <0.001)。GA + AA患者BChE活性明显低于GG患者(分别为3648.5 (2968-4332)mU/ml和7128.5 (6332-8341)mU/ml);0.001)。结论乳腺癌患者BCHE rs1803274 a型变异频率较高,BCHE活性较低,可能是乳腺癌发生的易感因素。此外,rs1803274与一些肿瘤特征有关,这可能是其预后价值的证明。
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来源期刊
Meta Gene
Meta Gene Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
1.10
自引率
0.00%
发文量
20
期刊介绍: Meta Gene publishes meta-analysis, polymorphism and population study papers that are relevant to both human and non-human species. Examples include but are not limited to: (Relevant to human specimens): 1Meta-Analysis Papers - statistical reviews of the published literature of human genetic variation (typically linked to medical conditionals and/or congenital diseases) 2Genome Wide Association Studies (GWAS) - examination of large patient cohorts to identify common genetic factors that influence health and disease 3Human Genetics Papers - original studies describing new data on genetic variation in smaller patient populations 4Genetic Case Reports - short communications describing novel and in formative genetic mutations or chromosomal aberrations (e.g., probands) in very small demographic groups (e.g., family or unique ethnic group). (Relevant to non-human specimens): 1Small Genome Papers - Analysis of genetic variation in organelle genomes (e.g., mitochondrial DNA) 2Microbiota Papers - Analysis of microbiological variation through analysis of DNA sequencing in different biological environments 3Ecological Diversity Papers - Geographical distribution of genetic diversity of zoological or botanical species.
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