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NAD(P)H:醌氧化还原酶多态性的鉴定及其与肺癌和吸烟的关联。

Identification of an NAD(P)H:quinone oxidoreductase polymorphism and its association with lung cancer and smoking.

作者信息

Rosvold E A, McGlynn K A, Lustbader E D, Buetow K H

机构信息

Division of Population Science, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

出版信息

Pharmacogenetics. 1995 Aug;5(4):199-206. doi: 10.1097/00008571-199508000-00003.

DOI:10.1097/00008571-199508000-00003
PMID:8528266
Abstract

The enzyme NAD(P)H:quinone oxidoreductase (NQO1) catalyses bioreduction and bioactivation reactions. A mutation in the NQO1 gene had previously been demonstrated in a cancer cell line with reduced NQO1 activity. In this study, several regions of the NQO1 locus were examined for constitutional variation at the DNA level. The previously described mutation in exon 6 was detected by the single-strand conformation polymorphism technique. This was confirmed by sequencing to result from a C-->T substitution. Genotype analysis in the Centre d'Etude Polymorphisme Humain (CEPH) reference panel revealed two alleles with frequencies of 0.87 and 0.13 and demonstrated Mendelian transmission. Genotype distributions were consistent with Hardy-Weinberg equilibrium. Linkage analysis mapped the gene locus to chromosome 16q. NQO1 was felt to be a candidate gene for the susceptibility to lung cancer, given its potential role in protection against carcinogenic compounds. The frequency of NQO1 variants was examined in 150 lung cancer cases and in two reference populations. The allele distribution in CEPH parent controls was significantly different from cases (chi 2 = 5.52, p = 0.019), but no difference was noted between cases and a healthy local reference population. When the local reference distribution was stratified on smoking status, a significant difference was observed (chi 2 = 3.88, p = 0.048).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

酶NAD(P)H:醌氧化还原酶(NQO1)催化生物还原和生物激活反应。先前已在NQO1活性降低的癌细胞系中证实了NQO1基因的突变。在本研究中,检测了NQO1基因座的几个区域在DNA水平上的结构变异。通过单链构象多态性技术检测到先前描述的外显子6中的突变。测序证实这是由C→T替换导致的。在人类多态性研究中心(CEPH)参考样本中的基因型分析显示有两个等位基因,频率分别为0.87和0.13,并证明了孟德尔遗传。基因型分布符合哈迪-温伯格平衡。连锁分析将该基因座定位到16号染色体q臂。鉴于NQO1在预防致癌化合物方面的潜在作用,它被认为是肺癌易感性的候选基因。在150例肺癌病例和两个参考人群中检测了NQO1变体的频率。CEPH亲本对照中的等位基因分布与病例有显著差异(χ2 = 5.52,p = 0.019),但病例与当地健康参考人群之间未发现差异。当根据吸烟状况对当地参考分布进行分层时,观察到显著差异(χ2 = 3.88,p = 0.048)。(摘要截短于250字)

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