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Association and functional study of ATP6V1D and GPHN gene polymorphisms with depression in Chinese population
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作者 Peng Liang Jing-Jie Chen +5 位作者 Xue Yang Rui Long Yue Li Zi-Ling Wang Ping-Liang Yang Yun-Dan Liang 《World Journal of Psychiatry》 2025年第4期73-85,共13页
BACKGROUND Depression is a disease with a significant global social burden.Single nucleotide polymorphisms(SNPs)are correlated with the development of depression.This study investigates the relationship between polymo... BACKGROUND Depression is a disease with a significant global social burden.Single nucleotide polymorphisms(SNPs)are correlated with the development of depression.This study investigates the relationship between polymorphisms in the GPHN and ATP6V1D gene promoter regions and susceptibility to depression in the Chinese population.AIM To provide new insights into identifying SNPs for predicting depression in the Chinese population.METHODS We conducted a case-control study involving 555 individuals with depression and 509 healthy controls.GPHN rs8020095 and ATP6V1D rs3759755,rs10144417,rs2031564,and rs8016024 in the promoter region were genotyped using nextgeneration sequencing.Dual luciferase reporter genes were employed to assess the transcriptional activity of promoter regions for each SNP genotype,with transcription factors binding to each site predicted using the JASPAR database.RESULTS Compared to healthy controls,the ATP6V1D promoter rs10144417 AG genotype (P = 0.015), rs3759755 AC/CC genotype (P = 0.036), and GPHN gene rs8020095 GA and AA genotypes (GA: P =0.028, GG: P = 0.025) were significantly associated with a lower prevalence of depression. Linked disequilibria werepresent in five SNPs, with the AGATA haplotype frequency in patients significantly lower than in healthy subjects(P = 0.023). Luciferase activity of the rs3759755-A recombinant plasmid was significantly higher than that of thers3759755-C recombinant plasmid (P = 0.026), and the rs8020095-A recombinant plasmid activity was significantlyhigher than that of the rs8020095-G recombinant plasmid (P = 0.001). Transcription factors orthodenticle homeobox2, orthodenticle homeobox 1, forkhead box L1, NK homeobox 3-1, and nuclear factor, interleukin 3 regulateddemonstrated binding affinity with rs3759755A > C and rs8020095A > G.CONCLUSIONThis study demonstrates that SNPs (rs3759755 and rs10144417) in the promoter region of the ATP6V1D and SNP(rs8020095) of GPHN are indeed associated with susceptibility to depression. 展开更多
关键词 Single nucleotide polymorphism Genetic susceptibility DEPRESSION ATP6V1D gphn
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桥蛋白基因对膀胱尿路上皮癌预后评估的意义及功能研究 被引量:2
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作者 曾梓航 李佳丽 +5 位作者 刘嘉彬 李硕 张冉 孟详喻 李胜 杜雪晴 《临床内科杂志》 CAS 2019年第1期19-22,共4页
目的 通过生物信息学方法对桥蛋白基因(GPHN)进行功能探讨,分析其药物敏感性,并通过生存分析判断其在膀胱尿路上皮癌(BLCA)预后评估中的意义.方法 在TCGA数据库获取BLCA的mRNA测序(mRNA-seq)及相应临床数据;利用R语言Survival程序包对G... 目的 通过生物信息学方法对桥蛋白基因(GPHN)进行功能探讨,分析其药物敏感性,并通过生存分析判断其在膀胱尿路上皮癌(BLCA)预后评估中的意义.方法 在TCGA数据库获取BLCA的mRNA测序(mRNA-seq)及相应临床数据;利用R语言Survival程序包对GPHN表达运用Kaplan-Meier法及Cox回归进行生存分析;联合基因表达文库数据库(GEO)多数据集对不同GPHN表达的BLCA患者进行Meta分析;对GPHN差异表达基因(DEGs)进行基因本体(GO)及京都基因与基因组百科全书(KEGG)富集分析;利用GSCALite工具获取基因与药物敏感的相关性信息.结果 生存分析显示GPHN表达对BLCA患者生存有显著影响(Kaplan-Meier法HR=1.735,P=0.004;Cox回归HR=1.002,P=0.002);富集出有关GO的生物功能条目172个,KEGG通路1条,均与肿瘤相关;GPHN对TGX221、AZD6482、XMD8-85、Salubrinal、Cyclopamine、A-770041药物敏感.结论 GPHN与BLCA的预后显著相关,其在BLCA中具有重要功能,可能作为其预后判断的生物标记物. 展开更多
关键词 膀胱尿路上皮癌 生物信息学 TCGA GEO gphn 富集分析
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