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细胞色素P450IA1(CypIA1)的血红素结合区域多态性,而非IIE1(CypIIE1)的RsaI多态性,与里约热内卢的肺癌相关。

The heme-binding region polymorphism of cytochrome P450IA1 (CypIA1), rather than the RsaI polymorphism of IIE1 (CypIIE1), is associated with lung cancer in Rio de Janeiro.

作者信息

Hamada G S, Sugimura H, Suzuki I, Nagura K, Kiyokawa E, Iwase T, Tanaka M, Takahashi T, Watanabe S, Kino I

机构信息

Epidemiology Division, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Cancer Epidemiol Biomarkers Prev. 1995 Jan-Feb;4(1):63-7.

PMID:7534543
Abstract

Ile-Val polymorphism in exon 7 of cytochrome P450IA1 (CypIA1) and RsaI polymorphism of cytochrome P450IIE1 (CypIIE1) were examined in a case-control study of lung cancer in Rio de Janeiro, Brazil. The Val-containing genotype in exon 7 of CypIA1 was found to be associated with lung cancer in this population (odds ratio, 2.26; 95% confidence interval, 1.14-4.47 for 99 cases versus 108 controls of 123 matched pairs), whereas RsaI polymorphism in CypIIE1 was not associated with lung cancer susceptibility. In squamous cell carcinoma, the degree of association of Val-containing genotype was greater in those with fewer pack-years of smoking. The RsaI polymorphism of CypIIE1 has a different distribution from the Japanese pattern and is not associated with lung cancer. When we analyzed the association of Ile-Val polymorphism to MspI polymorphism of CypIA1, the Val/Val homozygote was found only in the subpopulation with the MspI site-present homozygote. The apparent lack of association of CypIA1 MspI polymorphism with lung cancer in this area reported in our previous study and the results of the present study indicate that the "true" responsible site for lung cancer susceptibility should be the Ile-Val polymorphism in the catalytic site of CypIA1.

摘要

在巴西里约热内卢进行的一项肺癌病例对照研究中,检测了细胞色素P450IA1(CypIA1)第7外显子的异亮氨酸 - 缬氨酸多态性以及细胞色素P450IIE1(CypIIE1)的RsaI多态性。在该人群中发现,CypIA1第7外显子含缬氨酸的基因型与肺癌相关(优势比为2.26;95%置信区间,99例病例与123对匹配对照中的108例对照相比为1.14 - 4.47),而CypIIE1中的RsaI多态性与肺癌易感性无关。在鳞状细胞癌中,吸烟包年数较少者中含缬氨酸基因型的关联程度更大。CypIIE1的RsaI多态性分布与日本模式不同,且与肺癌无关。当我们分析CypIA1的异亮氨酸 - 缬氨酸多态性与MspI多态性的关联时,仅在具有MspI位点存在纯合子的亚群中发现了Val/Val纯合子。我们之前的研究报告了该地区CypIA1 MspI多态性与肺癌明显缺乏关联,而本研究结果表明,肺癌易感性的“真正”责任位点应该是CypIA1催化位点的异亮氨酸 - 缬氨酸多态性。

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