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Association between LAPTM4B gene polymorphism and susceptibility to and prognosis of diffuse large B-cell lymphoma

机译:LaptM4B基因多态性与弥漫性大B细胞淋巴瘤的易感性与易感性和预后的关联

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摘要

Lysosomal protein transmembrane 413 (LAPTM4B) is an oncogene that is overexpressed in a number of various types of human cancer. There are two known alleles of LAPTM4B: LAPTM4B*1 and LAPTM4B*2. The present study assessed the association between LAPTM4B polymorphisms and the susceptibility to diffuse large B-cell lymphoma (DLBCL) and its prognosis. LAPTM4B genotypes were determined using polymerase chain reaction analysis in 164 DLBCL and 350 healthy control cases. The association between LAPTM4B polymorphisms and the risk of DLBCL was analyzed using unconditional logistic regression. Differences in patient survival were calculated using Kaplan-Meier analysis. The present study indicated no significant differences (P0.05) in the frequency of LAPTM4B*2 alleles between DLBCL cases (26.5%) and controls (24.1%). The risk of DLBCL was slightly increased in cases with the LAPTM4B*1/2 genotype [odds ratio (OR)=1.160; 95% confidence interval (CI)=0.781-1.724] or the LAPTM4B*2/2 genotype (OR=1.446; 95% CI=0.648-3.227) compared with those with the LAPTM4B*1/1 genotype. There was no significant association between the presence of the LAPTM4B*2 allele and overall survival (OS) and disease-free survival (DFS) in patients with DLBCL (P=0.399 and 0.520, respectively). However, there was a tendency for patients with LAPTM4B*2 and International Prognostic Index (IPI) score 3-5 to have longer OS and DFS (P=0.126 and 0.109, respectively). These findings suggest that genetic polymorphisms of LAPTM4B is not a risk factor for the development of DLBCL, but the LAPTM4B*2 allele may a better prognostic indicator in patients with IPI score 3-5 in DLBCL.
机译:溶酶体蛋白跨膜413(LabeM4B)是一种在许多各种类型的人类癌症中过表达的癌基因。有两种已知的LableM4B等位基因:LabtM4B * 1和LabyM4B * 2。本研究评估了LaptM4B多态性与扩散大B细胞淋巴瘤(DLBCL)的易感性之间的关联及其预后。使用聚合酶链反应分析在164dlbcl和350个健康对照病例中测定LaptM4B基因型。使用无条件逻辑回归分析了LableM4B多态性与DLBCL风险之间的关联。使用Kaplan-Meier分析计算患者存活的差异。本研究表明,DLBCL病例(26.5%)和对照(24.1%)之间的LabeM4B * 2等位基因频率下没有显着差异(p> 0.05)。 LaptM4B * 1/2基因型[odds比率(或)= 1.160的情况下,DLBCL的风险略微增加; 95%置信区间(CI)= 0.781-1.724]或LabyM4B * 2/2基因型(或= 1.446; 95%CI = 0.648-3.227)与LabyM4B * 1/1基因型相比。 LaptM4B * 2等位基因的存在与DLBCL患者的LableM4B * 2等位基因和总体存活(OS)和无病生存(DFS)之间没有显着关联(分别分别为0.399和0.520)。然而,LaptM4B * 2和国际预后指数(IPI)得分3-5的患者倾向于具有较长的OS和DFS(P = 0.126和0.109)。这些发现表明LaptM4B的遗传多态性不是DLBCL发展的危险因素,但是LableM4B * 2等位基因可能在DLBCL中IPI评分3-5患者中更好的预后指标。

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