Asgerov Elmir, Şenol Özgür, Güler Adem, Berdeli Afig
Department of General Surgery, Ege University School of Medicine, İzmir, Turkey.
Molecular Medicine Laboratory, Ege University School of Medicine, İzmir, Turkey.
Turk J Gastroenterol. 2019 Jun;30(6):517-523. doi: 10.5152/tjg.2019.18100.
BACKGROUND/AIMS: Gastric cancers vary across countries and ethnic groups. They are the second most common type of cancer worldwide. Dietary and non-dietary factors as well as genetic and epigenetic alterations of many mechanisms are implicated in the development of gastric cancer. We aimed to determine the sequence of possible nucleotide changes, polymorphisms, and mutations, and to establish genotype and phenotype relation by performing whole DNA sequence analysis of the XRCC1 and ERCC1 genes belonging to base excision repair (BER) and nucleotide excision repair (NER) family of DNA repair genes in patients with gastric cancer.
We included 50 patients of both sexes who had received diagnosis of gastric cancer and 50 healthy people who showed same demographic traits that forms the control group. We analyzed the ERCC1 and XRCC1 genes by DNA sequence analysis on both groups. After the analysis, we compared the genotype-phenotype relation.
Neither patients nor the control group has any nucleotide replacement in any exon of ERCC1 genes. We could not detect significant difference between patients and healthy groups when we correlated genotype contribution of mutations Arg194Trp, Arg208His, Arg399Gln detected in the XRCC1 gene and allele frequency.
According to our study, the ERCC1 gene in Turkish population is not getting mutation in patients with gastric cancer and healthy individuals. Three mutations were detected in the XRCC1 gene, and these mutations were not associated with gastric cancer.
背景/目的:胃癌在不同国家和种族群体中存在差异。它是全球第二大常见癌症类型。饮食和非饮食因素以及许多机制的遗传和表观遗传改变都与胃癌的发生有关。我们旨在通过对胃癌患者中属于碱基切除修复(BER)和核苷酸切除修复(NER)家族的DNA修复基因的XRCC1和ERCC1基因进行全DNA序列分析,确定可能的核苷酸变化、多态性和突变序列,并建立基因型与表型的关系。
我们纳入了50例已确诊胃癌的患者(男女均有)和50例具有相同人口统计学特征的健康人作为对照组。我们对两组进行DNA序列分析以检测ERCC1和XRCC1基因。分析后,我们比较了基因型与表型的关系。
患者组和对照组的ERCC1基因任何外显子均未出现核苷酸替换。当我们将XRCC1基因中检测到的突变Arg194Trp、Arg208His、Arg399Gln的基因型贡献与等位基因频率进行关联分析时,未发现患者组和健康组之间存在显著差异。
根据我们的研究,土耳其人群中的胃癌患者和健康个体的ERCC1基因未发生突变。在XRCC1基因中检测到三个突变,且这些突变与胃癌无关。