Ahmadi Nahid, Ahmadi Seyyed Amir Yasin, Kheirollahi Abdolreza, Shahsavar Farhad
Student Research Committee Lorestan University of Medical Sciences, Khorramabad, Iran.
Preventive Medicine and Public Health Research Center Psychosocial Health Research Institute Iran University of Medical Sciences, Tehran, Iran.
Prostate Cancer. 2024 Sep 25;2024:3997576. doi: 10.1155/2024/3997576. eCollection 2024.
Genetic and environmental factors are involved in prostate cancer. The current study was conducted to study the relationship between , , and polymorphisms in the promoter of and inflammatory genes with prostate cancer.
As a genetic association study with a case-control design, the genomes of people living in Khorasan, Iran, were compared in two groups of cases and controls. The genotype of the polymorphism present in the gene promoter was investigated by the PCR-RFLP method. PCR-SSP was used to study the genotype of and polymorphisms present in the gene promoter. Odds ratio (OR) and 95% confidence interval (CI) were reported.
One mutant allele in polymorphism (AG) increased the chance of cancer (OR = 4.902, 95% CI = 2.70-8.87) and two mutant alleles (GG) increased more (OR = 7.174, 95% CI = 2.48-20.68). One mutant allele in polymorphism (CG) increased the chance of cancer (OR = 5.583, 95% CI = 3.04-10.22) and two mutant alleles (CC) increased more (OR = 9.571, 95% CI = 3.10-29.46). One mutant allele in polymorphism (CA) increased the chance of cancer (OR = 5.359, 95% CI = 2.95-9.70) and two mutant alleles (AA) increased more (OR = 7.083, 95% CI = 2.61-19.15) ( < 0.001).
According to the results, the mutant alleles in polymorphisms , , and alleles were associated with an increased chance of prostate cancer in this population.
遗传和环境因素与前列腺癌有关。本研究旨在探讨[具体基因1]、[具体基因2]和[具体基因3]炎症基因启动子多态性与前列腺癌之间的关系。
作为一项病例对照设计的基因关联研究,对生活在伊朗霍拉桑的人群基因组在病例组和对照组两组中进行比较。采用PCR-RFLP方法研究[具体基因1]基因启动子中存在的[具体多态性1]多态性的基因型。用PCR-SSP研究[具体基因2]基因启动子中存在的[具体多态性2]和[具体多态性3]的基因型。报告比值比(OR)和95%置信区间(CI)。
[具体多态性1]多态性中的一个突变等位基因(AG)增加了患癌几率(OR = 4.902,95% CI = 2.70 - 8.87),两个突变等位基因(GG)增加得更多(OR = 7.174,95% CI = 2.48 - 20.68)。[具体多态性2]多态性中的一个突变等位基因(CG)增加了患癌几率(OR = 5.583,95% CI = 3.04 - 10.22),两个突变等位基因(CC)增加得更多(OR = 9.571,95% CI = 3.10 - 29.46)。[具体多态性3]多态性中的一个突变等位基因(CA)增加了患癌几率(OR = 5.359,95% CI = 2.95 - 9.70),两个突变等位基因(AA)增加得更多(OR = 7.083,95% CI = 2.61 - 19.15)(P < 0.001)。
根据结果,[具体多态性1]、[具体多态性2]和[具体多态性3]等位基因中的突变等位基因与该人群中前列腺癌几率增加有关。