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急性髓系白血病多态性研究中的遗传易感性研究关联

Association of genetic predisposition studies in polymorphism studies in acute myeloid leukemia.

作者信息

Farasani Abdullah

机构信息

Biomedical Research Unit, Medical Center, Jazan University, Saudi Arabia.

Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, Jazan University, Jazan, Saudi Arabia.

出版信息

Saudi J Biol Sci. 2024 Mar;31(3):103917. doi: 10.1016/j.sjbs.2023.103917. Epub 2023 Dec 23.

Abstract

Cytochrome P450 Family 1 Subfamily A Member 1 (CYP1A1) gene is one of the sub-members of CYP450 family member and it encodes with the families of drug metabolizing enzyme families along with the cancers and leukemias. Among leukemias, AML is considered to be one of the important leukemia which attack the older adults. The aim of this study is to explore the role of A4889G polymorphism in CYP1A1 gene in acute myeloid leukemia (AML) in the Saudi population. This study was designed as an experimental case-control study in which 100 AML cases and 100 controls were selected. This in vivo study was carried out using genomic DNA extraction, polymerase chain reaction and agarose gel electrophoresis and then BsrDI restriction enzyme to digest the A4889G polymorphism of the PCR products. In this study, 200 subjects were digested and based on the appearance of the bands, genotypes were categorized. The attained data was used to calculate the clinical details as well as genotype analysis. The study results confirmed AG genotype (OR = 3.23, CI = 1.60-6.55, p = 0.0008), AG + GG (OR = 3.47, CI = 1.76-6.86, p = 0.0002) and GG + AA (OR = 12.47, CI = 6.18-15.17, p < 0.0001) and G vs A (OR = 3.15, CI = 1.71-5.81, p = 0.0001) were associated in AML cases. In conclusion, we confirm that A4889G polymorphism is associated with AML in the Saudi population.

摘要

细胞色素P450 1A1(CYP1A1)基因是细胞色素P450家族成员的亚成员之一,它与药物代谢酶家族以及癌症和白血病家族一起编码。在白血病中,急性髓系白血病(AML)被认为是侵袭老年人的重要白血病之一。本研究的目的是探讨沙特人群中CYP1A1基因A4889G多态性在急性髓系白血病(AML)中的作用。本研究设计为实验性病例对照研究,选取100例AML病例和100例对照。本体内研究通过基因组DNA提取、聚合酶链反应和琼脂糖凝胶电泳,然后用BsrDI限制性内切酶消化PCR产物的A4889G多态性。在本研究中,对200名受试者进行了消化,并根据条带的出现对基因型进行分类。所获得的数据用于计算临床细节以及基因型分析。研究结果证实,AML病例中AG基因型(比值比=3.23,置信区间=1.60 - 6.55,p = 0.0008)、AG + GG(比值比=3.47,置信区间=1.76 - 6.86,p = 0.0002)和GG + AA(比值比=12.47,置信区间=6.18 - 15.17,p < 0.0001)以及G与A(比值比=3.15,置信区间=1.71 - 5.81,p = 0.0001)相关。总之,我们证实A4889G多态性与沙特人群中的AML相关。

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Diagnostics (Basel). 2023 Oct 14;13(20):3214. doi: 10.3390/diagnostics13203214.
3
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Acta Biochim Pol. 2023 Sep 16;70(3):503-507. doi: 10.18388/abp.2020_6235.
4
Immune checkpoint-related gene polymorphisms are associated with acute myeloid leukemia.
Cancer Med. 2023 Sep;12(18):18588-18596. doi: 10.1002/cam4.6468. Epub 2023 Aug 21.
7
Effect of XRCC1 Arg399Gln Gene Polymorphism on Survival in Lymphoblastic Leukemia.
Asian Pac J Cancer Prev. 2023 May 1;24(5):1687-1693. doi: 10.31557/APJCP.2023.24.5.1687.
8
Phe354Leu polymorphism of the liver kinase B1 gene as a prognostic factor in adult egyptian patients with acute myeloid leukemia.
Heliyon. 2023 May 3;9(5):e15415. doi: 10.1016/j.heliyon.2023.e15415. eCollection 2023 May.
9
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10
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