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单核苷酸多态性有助于保护高加索人群免受非霍奇金淋巴瘤(NHL)的侵害。

Single Nucleotide Polymorphisms in Contribute to Protection Against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations.

机构信息

Genomics Research Centre, School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, QLD, Australia.

出版信息

Genes (Basel). 2019 Feb 27;10(3):185. doi: 10.3390/genes10030185.

Abstract

Recent studies show an association of microRNA (miRNA) polymorphisms (miRSNPs) in different cancer types, including non-Hodgkin lymphoma (NHL). The identification of miRSNPs that are associated with NHL susceptibility may provide biomarkers for early diagnosis and prognosis for patients who may not respond well to current treatment options, including the immunochemotherapy drug combination that includes rituximab, cyclophosphamide, doxorubicin, vincristine and prednisome (R-CHOP). We developed a panel of miRSNPs for genotyping while using multiplex PCR and chip-based mass spectrometry analysis in an Australian NHL case-control population (300 cases, 140 controls). Statistical association with NHL susceptibility was performed while using Chi-square (χ²) and logistic regression analysis. We identified three SNPs in MIR143 that are to be significantly associated with reduced risk of NHL: rs3733846 (odds ratio (OR) [95% confidence interval (CI)] = 0.54 [0.33 ⁻ 0.86], p = 0.010), rs41291957 (OR [95% CI] = 0.61 [0.39 ⁻ 0.94], p = 0.024), and rs17723799 (OR [95% CI] = 0.43 [0.26 ⁻ 0.71], p = 0.0009). One SNP, rs17723799, remained significant after correction for multiple testing (p = 0.015). Subsequently, we investigated an association between the rs17723799 genotype and phenotype by measuring target gene Hexokinase 2 (HKII) expression in cancer cell lines and controls. Our study is the first to report a correlation between miRSNPs in MIR143 and a reduced risk of NHL in Caucasians, and it is supported by significant SNPs in high linkage disequilibrium (LD) in a large European NHL genome wide association study (GWAS) meta-analysis.

摘要

最近的研究表明,微 RNA(miRNA)多态性(miRSNPs)与不同类型的癌症有关,包括非霍奇金淋巴瘤(NHL)。确定与 NHL 易感性相关的 miRSNPs 可能为那些可能对当前治疗方案(包括包含利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松的免疫化疗药物组合)反应不佳的患者提供早期诊断和预后的生物标志物。我们在澳大利亚 NHL 病例对照人群(300 例病例,140 例对照)中使用多重 PCR 和基于芯片的质谱分析开发了一组 miRNA SNP 基因分型。使用卡方(χ²)和逻辑回归分析进行与 NHL 易感性的统计学关联。我们在 MIR143 中发现了三个与 NHL 风险降低显著相关的 SNP:rs3733846(比值比(OR)[95%置信区间(CI)]=0.54 [0.33 ⁻ 0.86],p=0.010),rs41291957(OR [95% CI]=0.61 [0.39 ⁻ 0.94],p=0.024)和 rs17723799(OR [95% CI]=0.43 [0.26 ⁻ 0.71],p=0.0009)。在进行多次检验校正后,一个 SNP,rs17723799,仍然具有统计学意义(p=0.015)。随后,我们通过测量癌症细胞系和对照中的靶基因己糖激酶 2(HKII)的表达,研究了 rs17723799 基因型与表型之间的关联。我们的研究首次报道了 MIR143 中的 miRSNPs 与白种人 NHL 风险降低之间的相关性,并且得到了大型欧洲 NHL 全基因组关联研究(GWAS)荟萃分析中高度连锁不平衡(LD)的显著 SNP 的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43bc/6471575/318067368804/genes-10-00185-g001.jpg

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