Pliarchopoulou Kyriaki, Voutsinas Gerasimos, Papaxoinis George, Florou Katherine, Skondra Maria, Kostaki Konstantina, Roussou Paraskevi, Syrigos Konstantinos, Pectasides Dimitrios
Oncology Unit, Second Department of Internal Medicine, Ippokrateion Hospital, Athens, Greece.
Oncol Lett. 2012 Jun;3(6):1301-1306. doi: 10.3892/ol.2012.665. Epub 2012 Mar 30.
Lung cancer is the leading cause of cancer mortality worldwide and tobacco smoking has been established as its biggest risk factor. Cigarette smoke contains several carcinogens. Most of them need to be activated by phase I enzymes, such as cytochrome P450 (CYP), while phase II enzymes, such as glutathione S-transferases are responsible for the detoxification of activated forms. The present study aimed to determine the role of CYP1A1, GSTP1 and GSTM1 gene polymorphisms in smoking-related lung cancer risk. It also aimed to investigate the association of the above polymorphisms with clinicopathological parameters, as well as their effect on survival. One hundred newly diagnosed lung cancer patients with advanced disease and 125 healthy controls with a smoking history participated in the study. The participants were screened for the presence of the following polymorphisms: MspI (CYP1A1), Ile105Val (GSTP1) and GSTM1 deletion. The above polymorphisms were also examined with regards to gender, age, histological type and survival. GSTP1 Ile/Val and GSTM1-null genotypes were associated with increased lung cancer risk and the presence of the combination of the three non-wild-type genotypes increases susceptibility to lung cancer (OR 3.328, 95% CI=1.681-6.587, p=0.001). In the non-small cell lung cancer group, the GSTP1 homozygous variant was significantly associated with increased lung cancer risk (p=0.008) and shorter survival. The results of this study suggest that the GSTP1 Ile/Val genotype and GSTM1 deletion contribute to increased lung cancer susceptibility. Moreover, GSTP1 Val/Val genotype is associated with increased lung cancer risk and shorter survival in non-small cell lung cancer patients.
肺癌是全球癌症死亡的主要原因,吸烟已被确认为其最大的风险因素。香烟烟雾中含有多种致癌物。其中大多数需要由I相酶(如细胞色素P450,CYP)激活,而II相酶(如谷胱甘肽S-转移酶)则负责对激活形式进行解毒。本研究旨在确定CYP1A1、GSTP1和GSTM1基因多态性在吸烟相关肺癌风险中的作用。它还旨在研究上述多态性与临床病理参数的关联,以及它们对生存的影响。100名新诊断的晚期肺癌患者和125名有吸烟史的健康对照者参与了该研究。对参与者进行以下多态性筛查:MspI(CYP1A1)、Ile105Val(GSTP1)和GSTM1缺失。还就性别、年龄、组织学类型和生存情况对上述多态性进行了检查。GSTP1 Ile/Val和GSTM1缺失基因型与肺癌风险增加相关,三种非野生型基因型组合的存在增加了患肺癌的易感性(OR 3.328,95%CI = 1.681 - 6.587,p = 0.001)。在非小细胞肺癌组中,GSTP1纯合变异型与肺癌风险增加(p = 0.008)和生存期缩短显著相关。本研究结果表明,GSTP1 Ile/Val基因型和GSTM1缺失导致肺癌易感性增加。此外,GSTP1 Val/Val基因型与非小细胞肺癌患者的肺癌风险增加和生存期缩短相关。