Gumuskaya Perihan Ozkan, Ozkan Kamile, Ay Arzu, Sipahi Tammam, Uzun Hafize
Department of İnternal Medicine, University of Health Sciences, Prof. Dr. Cemil Tascioglu City Hospital, 34668 Istanbul, Turkey.
Department of Biophysics, Medical Faculty of Trakya University, 22030 Edirne, Turkey.
Medicina (Kaunas). 2025 Aug 22;61(9):1504. doi: 10.3390/medicina61091504.
: Many studies have demonstrated a relationship between cancer and the NAD(P)H quinone oxidoreductase 1 (NQO1) polymorphism. Lung cancer (LC) is one of the most common malignant diseases and is an expanding global health problem. This study aimed to evaluate the association between the NQO1 C609T polymorphism and LC risk, including its distribution across histopathological subtypes, and to assess its potential as a genetic susceptibility marker. : A prospective study was conducted on 75 LC patients and 65 healthy controls. In this study, the C > T polymorphism occurring at position 609 in the NQO1 gene was examined in Turkish patients with LC. Demographic data and laboratory findings were collected from the patients and the hospital laboratory system. : The genotype frequencies (CC, CT, and TT) in LC patients were 66.7%, 32.0%, and 1.3%, respectively, compared with 60.0%, 35.4%, and 4.6% in the control group. Chi-square analysis revealed no significant association between the NQO1 C609T polymorphism and LC risk ( = 0.433). No correlation was observed between genotype distribution and histopathological subtypes. All patients had a long history of smoking (mean: 38.45 ± 12.14 years and 1.63 ± 0.64 packs/day). This is the first study conducted in Turkish people to determine the relationship between the C > T polymorphism occurring at position 609 in the NQO1 gene and the risk of LC. The patients with LC, regardless of their histopathological type, showed no relationship with the polymorphism in the NQO1 gene. Further high-quality investigations with more detailed environmental exposure information and larger sample sizes are warranted to confirm our findings.
许多研究已经证实癌症与烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)醌氧化还原酶1(NQO1)基因多态性之间存在关联。肺癌(LC)是最常见的恶性疾病之一,并且是一个日益严重的全球健康问题。本研究旨在评估NQO1基因C609T多态性与肺癌风险之间的关联,包括其在不同组织病理学亚型中的分布,并评估其作为遗传易感性标志物的潜力。
对75例肺癌患者和65例健康对照者进行了一项前瞻性研究。在本研究中,对土耳其肺癌患者的NQO1基因第609位发生的C>T多态性进行了检测。从患者和医院实验室系统收集了人口统计学数据和实验室检查结果。
肺癌患者的基因型频率(CC、CT和TT)分别为66.7%、32.0%和1.3%,而对照组分别为60.0%、35.4%和4.6%。卡方分析显示NQO1基因C609T多态性与肺癌风险之间无显著关联(P=0.433)。未观察到基因型分布与组织病理学亚型之间存在相关性。所有患者均有长期吸烟史(平均:38.45±12.14年,1.63±0.64包/天)。这是第一项在土耳其人群中进行的研究,旨在确定NQO1基因第609位发生的C>T多态性与肺癌风险之间的关系。无论组织病理学类型如何,肺癌患者均与NQO1基因多态性无关。需要进一步进行高质量的研究,纳入更详细的环境暴露信息和更大的样本量,以证实我们的研究结果。