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CDH1基因472delA和-160C>A多态性与墨西哥人群弥漫型和肠型胃癌的关联

Association between the CDH1-472delA and -160C>A polymorphisms and diffuse and intestinal gastric cancer in a Mexican population.

作者信息

Bustos-Carpinteyro A R, Delgado-Figueroa N, Santiago-Luna E, Magaña-Torres M T, Sánchez-López J Y

机构信息

División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.

Programa de Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.

出版信息

Genet Mol Res. 2016 Sep 16;15(3):gmr8715. doi: 10.4238/gmr.15038715.

Abstract

Gastric cancer (GC), the third leading cause of cancer-related deaths in Mexico and worldwide, can be classified into diffuse (DGC) or intestinal (IGC) types based on its histological characteristics. DGC is characterized by reduced expression of the cell adhesion protein E-cadherin, which is encoded by CDH1. The -472delA (rs5030625) and -160C>A (rs16260) polymorphisms in CDH1 induce a decrease in gene transcription; in fact, these mutated alleles have been associated with GC in some populations, with conflicting results. The aim of this study was to determine the association between the CDH1 -472delA and -160C>A polymorphisms and DGC and IGC in Mexican patients. The study was conducted in 24, 23, 48, and 93 individuals with DGC and IGC, without GC (control), and belonging to the general Mexican population (GMP), respectively. The genotypes were obtained by polymerase chain reaction - restriction fragment length polymorphism and the obtained data analyzed using Arlequin 3.1. The frequencies of the mutated allele (A) of -472delA were 0.326, 0.318, 0.284, and 0.296 in the DGC, IGC, control, and GMP groups, respectively, and those of the -160C>A polymorphism were 0.174, 0.318, 0.313, and 0.280, respectively. The genotype and allele frequencies of the two polymorphisms did not differ significantly (P > 0.05) among DGC, IGC, and control subjects. Therefore, we concluded that the CDH1 -472delA and -160C>A polymorphisms are not associated with DGC or IGC in patients from western Mexico.

摘要

胃癌(GC)是墨西哥及全球癌症相关死亡的第三大主要原因,根据其组织学特征可分为弥漫型(DGC)或肠型(IGC)。DGC的特征是细胞粘附蛋白E-钙粘蛋白表达降低,该蛋白由CDH1编码。CDH1中的-472delA(rs5030625)和-160C>A(rs16260)多态性会导致基因转录减少;事实上,这些突变等位基因在一些人群中与GC相关,但结果相互矛盾。本研究的目的是确定墨西哥患者中CDH1 -472delA和-160C>A多态性与DGC和IGC之间的关联。该研究分别在24名、23名、48名和93名患有DGC和IGC、无GC(对照)且属于墨西哥普通人群(GMP)的个体中进行。通过聚合酶链反应-限制性片段长度多态性获得基因型,并使用Arlequin 3.1对所得数据进行分析。-472delA突变等位基因(A)在DGC、IGC、对照和GMP组中的频率分别为0.326、0.318、0.284和0.296,-160C>A多态性的频率分别为0.174、0.318、0.313和0.280。在DGC、IGC和对照受试者中,这两种多态性的基因型和等位基因频率没有显著差异(P>0.05)。因此,我们得出结论,墨西哥西部患者中CDH1 -472delA和-160C>A多态性与DGC或IGC无关。

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