-羟基类固醇脱氢酶1在头颈部鳞状细胞癌中的表达。

S Gronau, D Koenig Greger, M Jerg, H Riechelmann
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引用次数: 11

摘要

β -羟基类固醇脱氢酶1 (11β - hsd1)已被确定为最有效的烟草烟雾衍生致癌物之一NNK的主要解毒酶。如果不被11β - hsd1代谢,细胞色素p450单氧化酶2D6 (CYP2D6)激活NNK会产生一种亲电中间体,负责DNA损伤。11β - hsd1和CYP2D6表达的个体间差异已被发现影响肺癌易感性。本研究的目的是比较口咽癌患者和对照组咽组织中11β - hsd1 mRNA表达和CYP2D6代谢状况。采用RT-PCR方法检测20例口咽癌患者和15例非吸烟对照者11β - hsd1 mRNA的表达。使用RFLP评估CYP2D6基因的遗传多态性频率。发现11β - hsd1 mRNA在人咽黏膜中表达。它在暴露于烟草烟雾的粘膜中表达上调。在肿瘤组织中,11β - hsd1的表达明显低于未受影响的粘膜。CYP2D6基因多态性在患者和对照组中的频率分布相似。慢性烟草滥用导致11β - hsd1酶的诱导。肿瘤组织中11β - hsd1表达的减少可能是恶性转化细胞的结果。目前尚不清楚11β - hsd1的低表达是否会导致额外突变率的增加。
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11Beta-hydroxysteroid dehydrogenase 1 expression in squamous cell carcinomas of the head and neck.

11Beta-hydroxysteroid dehydrogenase 1 (11beta-HSD1) has been identified as a major detoxification enzyme of one of the most potent tobacco smoke-derived carcinogens, NNK. If not metabolized by 11beta-HSD1, activation of NNK by cytochrome p450 mono-oxidase 2D6 (CYP2D6) results in an electrophile intermediate responsible for DNA damage. Interindividual variability in the expression of 11beta-HSD1 and CYP2D6 has been found to influence the susceptibility to lung cancer. The aim of this study was to compare 11beta-HSD1 mRNA expression and CYP2D6 metabolizer status in pharyngeal tissues of patients with oropharyngeal carcinoma and controls. In 20 patients with oropharyngeal cancer and 15 non-smoking controls, the 11beta-HSD1 mRNA expression was assessed with RT-PCR. The frequency of genetic polymorphisms of the CYP2D6 gene was assessed using RFLP. It was found that 11beta-HSD1 mRNA is expressed in human pharyngeal mucosa. It is upregulated in mucosa exposed to tobacco smoke. In tumour tissues, 11beta-HSD1 expression was significantly lower than in non-affected mucosa. The frequency distribution of CYP2D6 gene polymorphisms was similar in patients and controls. Chronic tobacco abuse results in 11beta-HSD1 enzyme induction. A reduction of 11beta-HSD1 expression in tumour tissues could be a consequence of malignantly transformed cells. It remains unclear if the lower 11beta-HSD1 expression gives rise to an increased rate of additional mutations.

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