https://scholars.lib.ntu.edu.tw/handle/123456789/112044
標題: | 肝細胞癌4q染色體精細輿圖分析:初步分析 Fine Mapping of Hepatocellular Carcinoma Susceptibility Gene on 4q: Preliminary Analysis |
作者: | 林琦鈞 Lin, Ci-Jyun |
關鍵字: | 肝癌;4q染色體;精細輿圖分析;HCC;4q;fine mapping | 公開日期: | 2005 | 摘要: | 背景與目的:肝細胞癌(hepatocellular carcinoma, HCC)為一種受到許多環境與遺傳因子影響之複雜性疾病。過去已有許多的loss-of-heterozygosity的研究指出在4q染色體上存在與HBV相關之HCC抑癌基因。本研究室先前的連鎖分析已在4q25位置發現初步顯著連鎖訊息。 材料與方法:我們以連鎖高峰為中心橫跨10 cM區域進行相關性研究,選擇14個單核苷多型性(single nucleotide polymorphism, SNPs)標記,分別對989名HBsAg陽性男性病例及956名HBsAg陽性之男性對照個案進行分析。 結果:以發病年齡進行分層分析,我們發現在發病年齡介於41~50歲之早發型的HCC中,SNP2在發病年齡介於41~50歲中,即使在校正多重檢定後仍具有顯著意義(P =.0003)。以相鄰標記進行半套體分析中,發現SNP1-SNP2在發病年齡介於41~50歲 (P value=.0006)及SNP8-SNP9在發病年齡>60歲 (P value=.0009)之半套体經過校正多重檢定後仍具有顯著意義。 結論:本研究發現SNP1-SNP2及SNP9-SNP9半套體和HCC顯著相關,但由於本研究的基因標記之分佈密度不夠密集,且涵蓋的區域不夠廣闊,未來有必要選取分佈更密且涵蓋更廣的SNP標記進行分析。 Background and Aim: Hepatocellular carcinoma (HCC) is a complex disease involving both environmental and genetic factors. Several loss-of-heterozygosity studies have suggested the existence of a tumor suppressor gene for HBV-related HCC on chromosome 4q. Our previous linkage study in HCC multiplex families has found a significant linkage signal on 4q25. The aim of this present study was to finely map the presumed HCC-susceptibility locus on 4q by using a large-scale case-control study. Materials and Method: A total of 989 male HBsAg-positive HCC cases and 956 age-sex matched HBsAg-positive controls were included. We analyzed 14 single nucleotide polymorphisms (SNPs) distributed throughout the 2-HLOD-drop internal (~10 cM) around the linkage peak identified by our previous study. Result: overall, none of the 14 SNPs were associated with HCC. However, SNP2 was significantly associated with early-onset HCC diagnosed between 41-50 years of age (P=.0003) this association remained statistically significant even after adjusting multiple comparisons by use of calculating false discovery rate. Haplotype analysis revealed that haplotype SNP1-SNP2 was associated with HCC diagnosed between 41-50 years of age (P=.0006), and SNP8-SNP9 was associated with HCC diagnosed at age >60 (P=0.0009). Conclusions: We found haplotypes SNP1-SNP2 and SNP8-SNP9 were significantly associated with HCC. Further association study with a higher density of markers, which focused on a broader chromosomal region, is warranted. |
URI: | http://ntur.lib.ntu.edu.tw//handle/246246/56231 | 其他識別: | zh-TW |
顯示於: | 流行病學與預防醫學研究所 |
檔案 | 描述 | 大小 | 格式 | |
---|---|---|---|---|
ntu-94-R92842008-1.pdf | 23.31 kB | Adobe PDF | 檢視/開啟 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。