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Association of CYP3A4, CYP3A5 polymorphisms with lung cancer risk in Bangladeshi population.

机译:CYP3A4,CYP3A5多态性与孟加拉人群肺癌风险的相关性。

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The rate of direct smoking, second hand smoking, and smokeless tobacco users as well as the amount of environmental pollutant like polycyclic aromatic hydrocarons is increasing in Bangladesh. Therefore, the prevalence of lung cancer is increasing day by day. To the best of our knowledge, no pharmacogentic study of CYP3A4, CYP3A5 genes has been reported on Bangladeshi population relating those with lung cancer. The present study was conducted to determine the association of CYP3A4, CYP3A5 gene polymorphisms and tobacco smoking in the development of lung cancer in Bangladeshi population. A case-control study was carried out on 106 lung cancer patients and 116 controls to investigate three allelic variants-CYP3A4*1B, CYP3A5*3, and CYP3A5*6 using Polymerase Chain Reaction Restriction Fragment Length Polymorphism. Risk of lung cancer was estimated as odds ratio (OR) and 95 % confidence interval (CI) using unconditional logistic regression models. The variant allele frequencies for CYP3A4*1B (*1A/*1B?+?*1B/*1B) were 2.83 % and 0.86 % and that of CYP3A5*3 (*1A/*3 +?*3/*3) were 88.68 % and 85.34 % in cases and controls, respectively. Individual carrying at least one variant allele of CYP3A4*1B (CYP3A4*1A/1B?+?*1B/1B) has a 3.35 times more risk (OR = 3.35, 95 % Cl = 0.34-32.71, p = 0.271) for developing lung cancer whereas individual carrying at least one variant allele of CYP3A5 (CYP3A5*1A/3 +?*3/3) has a 1.26 times more risk (OR = 1.35, 95 % Cl = 0.61-2.97) and both are statistically non-significant (p > 0.05). CYP3A5*6 was absent in the study population. No association of lung cancer with the mentioned polymorphisms was found both in heavy and light smokers. In the cases of all three major types of lung cancer-squamous cell carcinoma, adenocarcinoma, and small cell carcinoma-significantly strong relationships (p ? 0.05) have been found. To confirm the association of lung cancer with the mentioned polymorphisms, large number volunteers (patients and controls) will be required.
机译:在孟加拉国,直接吸烟,二手烟和无烟烟草使用者的比例以及诸如多环芳族水溶氢等环境污染物的数量正在增加。因此,肺癌的患病率每天都在增加。据我们所知,尚未有关于孟加拉国人群中与肺癌相​​关的CYP3A4,CYP3A5基因药理学研究的报道。本研究旨在确定CYP3A4,CYP3A5基因多态性与吸烟在孟加拉国人群肺癌的发生中的关系。使用聚合酶链反应限制片段长度多态性对106位肺癌患者和116位对照进行了病例对照研究,以研究3个等位基因变体CYP3A4 * 1B,CYP3A5 * 3和CYP3A5 * 6。使用无条件逻辑回归模型将肺癌风险估计为优势比(OR)和95%置信区间(CI)。 CYP3A4 * 1B(* 1A / * 1B?+?* 1B / * 1B)的变异等位基因频率为2.83%和0.86%,而CYP3A5 * 3(* 1A / * 3 +?* 3 / * 3)的变异等位基因频率为病例和对照分别为88.68%和85.34%。携带至少一种CYP3A4 * 1B(CYP3A4 * 1A / 1B?+?* 1B / 1B)变异等位基因的个体患病风险高3.35倍(OR = 3.35,95%Cl = 0.34-32.71,p = 0.271)肺癌,而携带至少一种CYP3A5等位基因(CYP3A5 * 1A / 3 +?* 3/3)的个体患病风险高1.26倍(OR = 1.35,95%Cl = 0.61-2.97),且两者在统计学上均不显着(p> 0.05)。在研究人群中不存在CYP3A5 * 6。在重度吸烟者和轻度吸烟者中均未发现肺癌与上述多态性相关。在所有三种主要类型的肺癌中,鳞状细胞癌,腺癌和小细胞癌之间的关系非常明显(p <0.05)。为了确认肺癌与上述多态性的关联,将需要大量志愿者(患者和对照)。

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