Shi Wei-Xing, Chen Shu-Qing
Department of Public Health, School of Medicine, Zhejiang University, Hangzhou 310031, Zhejiang Province, China.
World J Gastroenterol. 2004 Jul 1;10(13):1961-3. doi: 10.3748/wjg.v10.i13.463.
To investigate the association between cytochrome P450 2C19 (CYP2C19) gene polymorphism and cancer susceptibility by genotyping of CYP2C19 poor metabolizers (PMs) in cancer patients.
One hundred and thirty-five cases of esophagus cancer, 148 cases of stomach cancer, 212 cases of lung cancer, 112 cases of bladder cancer and 372 controls were genotyped by allele specific amplification-polymerase chain reaction (ASA-PCR) for CYP2C19 PMs. The frequencies of PMs in cancer groups and control group were compared.
The frequencies of PMs of CYP2C19 were 34.1%(46/135) in the group of esophagus cancer patients, 31.8%(47/148) in the stomach cancer patients, 34.4%(73/212) in the group of lung cancer patients, only 4.5%(5/112) in the bladder cancer patients and 14.0%(52/372) in control group. There were statistical differences between the cancer groups and control group (esophagus cancer, chi(2)=25.65, P<0.005, OR=3.18, 95%CI=2.005-5.042; stomach cancer, chi(2)=21.70, P<0.005, OR=2.86, 95%CI=1.820-4.501; lung cancer, chi(2)=33.58, P<0.005, OR=3.23, 95%CI=1.503-6.906; bladder cancer, chi(2)=7.50, P<0.01, OR=0.288, 95%CI=0.112-0.740).
CYP2C19 PMs have a high incidence of esophagus cancer, stomach cancer and lung cancer, conversely they have a low incidence of bladder cancer. It suggests that CYP2C19 may participate in the activation of procarcinogen of esophagus cancer, stomach cancer and lung cancer, but may involve in the detoxification of carcinogens of bladder cancer.
通过对癌症患者细胞色素P450 2C19(CYP2C19)慢代谢者(PMs)进行基因分型,研究CYP2C19基因多态性与癌症易感性之间的关联。
采用等位基因特异性扩增-聚合酶链反应(ASA-PCR)对135例食管癌患者、148例胃癌患者、212例肺癌患者、112例膀胱癌患者及372例对照者进行CYP2C19 PMs基因分型。比较癌症组与对照组中PMs的频率。
食管癌患者中CYP2C19 PMs的频率为34.1%(46/135),胃癌患者中为31.8%(47/148),肺癌患者中为34.4%(73/212),膀胱癌患者中仅为4.5%(5/112),对照组中为14.0%(52/372)。癌症组与对照组之间存在统计学差异(食管癌,χ²=25.65,P<0.005,OR=3.18,95%CI=2.005-5.042;胃癌,χ²=21.70,P<0.005,OR=2.86,95%CI=1.820-4.501;肺癌,χ²=33.58,P<0.005,OR=3.23,95%CI=1.503-6.906;膀胱癌,χ²=7.50,P<0.01,OR=0.288,95%CI=0.112-0.740)。
CYP2C19 PMs在食管癌、胃癌和肺癌中的发生率较高,而在膀胱癌中的发生率较低。这表明CYP2C开19可能参与食管癌、胃癌和肺癌致癌物的激活,但可能参与膀胱癌致癌物的解毒。