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巴基斯坦头颈癌患者中OGG1基因序列变异

OGG1 gene sequence variation in head and neck cancer patients in Pakistan.

作者信息

Mahjabeen Ishrat, Baig Ruqia Mehmood, Masood Nosheen, Sabir Maimoona, Malik Faraz Arshad, Kayani Mahmood Akhtar

机构信息

Cancer Genetics Lab, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.

出版信息

Asian Pac J Cancer Prev. 2011;12(10):2779-83.

Abstract

In Pakistani culture tobacco use is very high and a well known risk factor for developing head and neck cancer (HNC), tobacco smoke containing high quantities of chemical carcinogens such as aromatic amines and reactive oxygen species. OGG1 is the primary enzyme in the base excision repair (BER) pathway, responsible for the excision of 7, 8-dihydro-8-oxoguanine, a mutagenic base byproduct that occurs as a result of exposure to reactive oxygen species. Groups of 300 already diagnosed HNC patients along with normal controls were included in this study. PCR-single-strand conformation polymorphism and DNA sequencing were used to analyze the whole coding region of OGG1 gene. Sequence analysis revealed eight novel mutations (six missense and two frame shift mutations). Frequencies of missense mutations, Asp267Asn, Ser279Gly and Ile253Phe were 0.12, 0.13 and 0.06 respectively. Frequencies of other missense mutations, 1578A> T, 1582C> T and Ala399Glu (1542C> A) were 0.13, 0.13 and 0.16, whereas values for the frame shift mutations 1582insG and 1543-1544delCT were 0.13 and 0.16. In our study, incidence of these mutations was found higher in oral cancers (p<0.002) and in smokers (p<0.002) when compared with other sites of HNC and nonsmokers, respectively. Our finding suggests that these germline mutations in OGG1 gene contribute to risk of developing HNC.

摘要

在巴基斯坦文化中,烟草使用率很高,是导致头颈癌(HNC)的一个众所周知的风险因素,烟草烟雾中含有大量化学致癌物,如芳香胺和活性氧物质。OGG1是碱基切除修复(BER)途径中的主要酶,负责切除7,8 - 二氢 - 8 - 氧代鸟嘌呤,这是一种由于暴露于活性氧物质而产生的诱变碱基副产物。本研究纳入了300名已确诊的HNC患者以及正常对照。采用聚合酶链反应 - 单链构象多态性和DNA测序分析OGG1基因的整个编码区。序列分析发现了8个新突变(6个错义突变和2个移码突变)。错义突变Asp267Asn、Ser279Gly和Ile253Phe的频率分别为0.12、0.13和0.06。其他错义突变1578A>T、1582C>T和Ala399Glu(1542C>A)的频率为0.13、0.13和0.16,而移码突变1582insG和1543 - 1544delCT的值为0.13和0.16。在我们的研究中,与HNC的其他部位和非吸烟者相比,这些突变在口腔癌患者(p<0.002)和吸烟者(p<0.002)中的发生率更高。我们的研究结果表明,OGG1基因中的这些种系突变会增加患HNC的风险。

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