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溶酶体相关4次跨膜蛋白质基因多态性与肝癌易感性的关系 被引量:1
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作者 孙桂珍 李卓 +3 位作者 郝娃 牛京勤 殷继明 严艳 《世界华人消化杂志》 CAS 北大核心 2008年第8期908-911,共4页
目的:探讨溶酶体相关4次跨膜蛋白质B(lysosome-associated protein transmembrane 4 beta,LAPTM4B)基因多态性与肝癌易感性的关系.方法:应用病例对照研究方法,收集190例肝癌患者、190例慢性乙型肝炎患者、175例健康献血者全血,... 目的:探讨溶酶体相关4次跨膜蛋白质B(lysosome-associated protein transmembrane 4 beta,LAPTM4B)基因多态性与肝癌易感性的关系.方法:应用病例对照研究方法,收集190例肝癌患者、190例慢性乙型肝炎患者、175例健康献血者全血,分离白细胞,提取基因组DNA,采用特异性引物PCR方法,扩增LAPTM4B第一外显子5′UTR内的部分序列,对三组人群进行分析研究.x^2检验分析肝癌组与对照组LAPTM4B的基因多态性和其他相关因素的相关性.结果:LAPTM4B等位基因在三组观察对象中的分布,^*1和^*2在健康对照组的频率分别是75.71%和24.29%,慢肝组73.16%和26、84%,肝癌组中66.84%和33.45%,三组比较等位基因分布频率有统计学意义,健康对照组与肝癌组比较有统计学意义(x^2=6.979,P=0.008).LAPTM4B的基因型LAPTM4B1^*1型、LAPTM4B^*1/2混合型和LAPTM482^*2型在肝癌组中的频率分别是37.9%、57.9%和4.2%、慢肝组50.5%、45.3%和4.2%、健康对照组56.6%、38.3%和5.1%,三组间三种基因型分布频率比较有统计学意义(x^2=14.854,P〈0.005).结论:基因型^*1/2和等位基因^*2可能与肝癌的发生有关. 展开更多
关键词 肝癌易感性 基因多态性 乙型肝炎 溶酶体相关4次跨膜蛋白质B
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亚太地区抑癌基因p16及runx3甲基化与肝癌易感性关系的Meta分析
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作者 刘爽 新燕 富红丹 《内蒙古医科大学学报》 2016年第5期433-437,共5页
目的:应用Meta分析的方法评价亚太地区抑癌基Np16及runx3甲基化与肝癌易感性的关系。方法:检索1978。2014年在Medline、Pubmed数据库以及1994~2014年CNKI、中国生物医学文献数据库、万方和维普数据库收录的所有有关p16及runx3甲基化... 目的:应用Meta分析的方法评价亚太地区抑癌基Np16及runx3甲基化与肝癌易感性的关系。方法:检索1978。2014年在Medline、Pubmed数据库以及1994~2014年CNKI、中国生物医学文献数据库、万方和维普数据库收录的所有有关p16及runx3甲基化与肝癌研究的文献,并用Review Manager软件进行统计分析。结果:纳入国内外标准的文献共21篇,研究runx3基因的有8篇,研究p16基因的有13篇。数据合并结果显示,p16、runx3病例组与对照组甲基化的比值比(OR)分别为17.24和6.33,95%C1分别为(7.54-39.40)和(3.79-10.58);经统计学分析差异都具统计学意义(P〈0.05)。结论:p16及runx3甲基化与肝癌发生有密切关系。 展开更多
关键词 P16基因 RUNX3基因 甲基化 肝癌易感性 META分析
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DNA修复基因多态性与肝癌易感性研究进展 被引量:2
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作者 刘雯 胡志坚 《中国公共卫生》 CAS CSCD 北大核心 2009年第11期1315-1317,共3页
关键词 肝癌易感性 DNA修复基因 基因多态性
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p53 codon 72 polymorphism and liver cancer susceptibility: A meta-analysis of epidemiologic studies 被引量:5
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作者 Xi Chen Fei Liu Bo Li Yong-Gang Wei Lv-Nan Yan Tian-Fu Wen 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第9期1211-1218,共8页
AIM:To evaluate the association between p53 codon 72 polymorphism and liver cancer risk by means of meta-analysis. METHODS:Two investigators independently searched the Medline,Embase and Chinese Biomedicine databases.... AIM:To evaluate the association between p53 codon 72 polymorphism and liver cancer risk by means of meta-analysis. METHODS:Two investigators independently searched the Medline,Embase and Chinese Biomedicine databases.Summary odds ratios and 95%CI for p53 codon 72 polymorphism and liver cancer were calculated in fixedeffects model(Mantel-Haenszel method)and randomeffects model(DerSimonian and Laird method)when appropriate. RESULTS:This meta-analysis included 1115 liver cancer cases and 1778 controls.The combined results based on all studies showed that there was a statistically significant link between Pro/Pro genotype and liver cancer,but not between Arg/Arg or Pro/Arg genotype and liver cancer.When stratifying for race,similar results were obtained,i.e.patients with liver cancer had a significantly higher frequency of Pro/Pro genotype than non-cancer patients among Asians.After stratifying thevarious studies by control source,gender,family history of liver cancer and chronic hepatitis virus infection,we found that(1)patients among hospital-based studies had a significantly higher frequency of Pro/Pro and a significantly lower frequency of Arg/Arg genotype than individuals without cancer;(2)female patients with liver cancer had a significantly lower frequency of Arg/Arg and a higher frequency of Pro/Arg+Pro/Pro genotypes than female individuals without cancer;(3)subgroup analyses for family history of liver cancer did not reveal any significant association between p53 codon 72 polymorphism and liver cancer development;and(4) patients with negative hepatitis virus infection had a significantly higher frequency of Pro/Pro and a significantly lower frequency of Arg/Arg genotype than individuals without cancer. CONCLUSION:This meta-analysis suggests that the p53 codon 72 polymorphism may be associated with liver cancer among Asians. 展开更多
关键词 Liver cancer p53 codon 72 Gene polymorphism META-ANALYSIS
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Interleukin-10 gene polymorphisms and hepatocellular carcinoma susceptibility:A meta-analysis 被引量:3
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作者 Yong-Gang Wei, Fei Liu, Bo Li, Xi Chen, Yu Ma, Lv-Nan Yan, Tian-Fu Wen, Ming-Qing Xu, Wen-Tao Wang, Jia-Yin YangYong-Gang Wei, Fei Liu, Bo Li, Xi Chen, Yu Ma, Lv-Nan Yan, Tian-Fu Wen, Ming-Qing Xu, Wen-Tao Wang, Jia-Yin Yang, Department of Liver and Vascular Surgery, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Prov- ince, China Author contributions: Wei YG and Liu F designed the study, collected and analyzed the data and wrote the manuscript Li B collected and analyzed the data and wrote the manuscript +4 位作者 Chen X and Ma Y collected and analyzed the data Yan LN analyzed the data and contributed to the discussion Wen TF and Xu MQ revised the manuscript Wang WT and Yang JY contributed to the discussion Wei YG and Liu F contributed equally to this work. 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第34期3941-3947,共7页
AIM: To assess the association between Interleu-kin-10 (IL-10) gene IL-10-1082 (G/A), IL-10-592(C/A), IL-10-819 (T/C) polymorphisms and hepatocellular carcinoma (HCC) susceptibility.METHODS: Two investigators independ... AIM: To assess the association between Interleu-kin-10 (IL-10) gene IL-10-1082 (G/A), IL-10-592(C/A), IL-10-819 (T/C) polymorphisms and hepatocellular carcinoma (HCC) susceptibility.METHODS: Two investigators independently searched the Medline, Embase, China National Knowledge Infrastructure, and Chinese Biomedicine Database. Summary odds ratios (ORs) and 95% conf idence intervals (95% CIs) for IL-10 polymorphisms and HCC were cal-culated in a fixed-effects model (the Mantel-Haenszel method) and a random-effects model (the DerSimonian and Laird method) when appropriate. RESULTS: This meta analysis included seven eligiblestudies, which included 1012 HCC cases and 2308 controls. Overall, IL-10-1082 G/A polymorphism was not associated with the risk of HCC (AA vs AG + GG, OR = 1.11, 95% CI = 0.90-1.37). When stratifying for ethnicity, the results were similar (Asian, OR = 1.12, 95% CI = 0.87-1.44; non-Asian, OR = 1.10, 95% CI = 0.75-1.60). In the overall analysis, the IL-10 polymorphism at position -592 (C/A) was identified as a genetic risk factor for HCC among Asians; patients carrying the IL-10-592*C allele had an increased risk of HCC (OR = 1.29, 95% CI = 1.12-1.49). No association was observed between the IL-10-819 T/C polymorphism and HCC susceptibility (TT vs TC + CC, OR = 1.02, 95% CI = 0.79-1.32).CONCLUSION: This meta-analysis suggests that IL-10-592 A/C polymorphism may be associated with HCC among Asians. IL-10-1082 G/A and IL-10-819 T/C polymorphisms were not detected to be related to the risk for HCC. 展开更多
关键词 Hepatocellular carcinoma Interleukin-10 Gene polymorphism Meta-analysis
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