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Association between two single nucleotide polymorphisms of the Prostaglandin-Endoperoxide Synthase 1 and 2 genes and cell proliferative prostatic diseases in Lebanon.前列腺素内过氧化物合酶1和2基因的两个单核苷酸多态性与黎巴嫩细胞增殖性前列腺疾病之间的关联。
Oncotarget. 2025 Apr 4;16:262-272. doi: 10.18632/oncotarget.28710.
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本文引用的文献

1
Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
CA Cancer J Clin. 2024 May-Jun;74(3):229-263. doi: 10.3322/caac.21834. Epub 2024 Apr 4.
2
The Efficacy of Cyclooxygenase-2 Inhibitors for the Male Treatment of Lower Urinary Tract Symptoms: A Systematic Review and Meta-Analysis.环氧化酶-2 抑制剂治疗男性下尿路症状的疗效:系统评价和荟萃分析。
Am J Mens Health. 2023 May-Jun;17(3):15579883231176667. doi: 10.1177/15579883231176667.
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The global, regional, and national burden of benign prostatic hyperplasia in 204 countries and territories from 2000 to 2019: a systematic analysis for the Global Burden of Disease Study 2019.2000 年至 2019 年全球 204 个国家和地区良性前列腺增生的全球、区域和国家负担:2019 年全球疾病负担研究的系统分析。
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4
Prostate Cancer Incidence and Mortality: Global Status and Temporal Trends in 89 Countries From 2000 to 2019.前列腺癌发病率和死亡率:2000 年至 2019 年 89 个国家的全球状况和时间趋势。
Front Public Health. 2022 Feb 16;10:811044. doi: 10.3389/fpubh.2022.811044. eCollection 2022.
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Prevalence of benign prostatic hyperplasia among the adult general population of five Middle Eastern Countries: Results of the SNAPSHOT programme.五个中东国家成年普通人群中良性前列腺增生的患病率:SNAPSHOT项目的结果。
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Cancer in Lebanon: A Review of Incidence Rates from 2008 to 2015 and Projections Till 2025.黎巴嫩的癌症:2008年至2015年发病率回顾及至2025年的预测
South Asian J Cancer. 2020 Jul;9(3):147-152. doi: 10.1055/s-0040-1721291. Epub 2020 Dec 14.
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Extreme Polygenicity of Complex Traits Is Explained by Negative Selection.复杂性状的极端多基因性是由负选择解释的。
Am J Hum Genet. 2019 Sep 5;105(3):456-476. doi: 10.1016/j.ajhg.2019.07.003. Epub 2019 Aug 8.
8
Benefits and limitations of genome-wide association studies.全基因组关联研究的优势和局限性。
Nat Rev Genet. 2019 Aug;20(8):467-484. doi: 10.1038/s41576-019-0127-1.
9
Roles of Cyclooxygenase-2 gene -765G > C (rs20417) and -1195G > A (rs689466) polymorphisms in gastric cancer: A systematic review and meta-analysis.环氧化酶-2 基因 -765G > C(rs20417)和-1195G > A(rs689466)多态性在胃癌中的作用:系统评价和荟萃分析。
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10
Downregulation of cyclooxygenase‑1 stimulates mitochondrial apoptosis through the NF‑κB signaling pathway in colorectal cancer cells.环氧合酶‑1 的下调通过 NF‑κB 信号通路刺激结直肠癌细胞中的线粒体凋亡。
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前列腺素内过氧化物合酶1和2基因的两个单核苷酸多态性与黎巴嫩细胞增殖性前列腺疾病之间的关联。

Association between two single nucleotide polymorphisms of the Prostaglandin-Endoperoxide Synthase 1 and 2 genes and cell proliferative prostatic diseases in Lebanon.

作者信息

Sheehan Brock J, Edwards Bryson, Medrano Ivanna Soto, El-Saidi Mohammed A, Zaidan Wissam R, El-Ezzi Asmahan A, Kuddus Ruhul H

机构信息

Department of Biology, Utah Valley University, Orem, UT 84058, USA.

Department of Strategic Management and Operations, Utah Valley University, Orem, UT 84058, USA.

出版信息

Oncotarget. 2025 Apr 4;16:262-272. doi: 10.18632/oncotarget.28710.

DOI:10.18632/oncotarget.28710
PMID:40184332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11970937/
Abstract

The polymorphic genes PTGS1 and PTGS2 encode cyclooxygenases COX-1 and COX-2, respectively. Overexpression of these cyclooxygenases is linked to inflammation and neoplasms. This study investigated the potential association between the single nucleotide polymorphism (SNP) -842A>G (rs10306114) of the PTGS1 gene and SNP-765G>C (rs20417) of the PTGS2 gene with prostate cancer (PCa) and benign prostate hyperplasia (BPH). Blood leucocyte DNA from 56 healthy individuals, 61 individuals with PCa, and 51 individuals with BPH were genotyped using the PCR-RFLP method. Associations were inferred by calculating odds ratios (OR) and relative risks (RR) of genotype distributions and allele frequencies. The genotypes for both SNPs were in Hardy-Weinberg equilibrium for all groups. No significant association was observed between the A or G alleles or the AA, AG, or GG genotypes of the SNP-842A>G of the PTGS1 gene and prostatic diseases. However, the C allele of SNP-765G>C of the PTGS2 gene was significantly associated with an increased risk of BPH (OR = 2.30, -value = 0.01). Differences in the ratios of GG/GC and GG/(GC+CC) genotypes also suggested a potential association between the C allele and PCa (-value <0.1), and the combined affected (PCa+BPH) group (-value <0.04). The small sample size and sampling from one ethnic group are limitations of this study.

摘要

多态性基因PTGS1和PTGS2分别编码环氧化酶COX - 1和COX - 2。这些环氧化酶的过表达与炎症和肿瘤有关。本研究调查了PTGS1基因的单核苷酸多态性(SNP)-842A>G(rs10306114)和PTGS2基因的SNP - 765G>C(rs20417)与前列腺癌(PCa)和良性前列腺增生(BPH)之间的潜在关联。使用PCR - RFLP方法对56名健康个体、61名PCa患者和51名BPH患者的血液白细胞DNA进行基因分型。通过计算基因型分布和等位基因频率的优势比(OR)和相对风险(RR)来推断关联。所有组中两个SNP的基因型均处于哈迪 - 温伯格平衡。未观察到PTGS1基因的SNP - 842A>G的A或G等位基因或AA、AG或GG基因型与前列腺疾病之间存在显著关联。然而,PTGS2基因的SNP - 765G>C的C等位基因与BPH风险增加显著相关(OR = 2.30,P值 = 0.01)。GG/GC和GG/(GC + CC)基因型比例的差异也表明C等位基因与PCa(P值 <0.1)以及合并受累(PCa + BPH)组(P值 <0.04)之间存在潜在关联。本研究的局限性在于样本量小且来自单一民族。