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ATBF1的下调是肝细胞癌的主要失活机制。

Down-regulation of ATBF1 is a major inactivating mechanism in hepatocellular carcinoma.

作者信息

Kim C J, Song J H, Cho Y G, Cao Z, Lee Y S, Nam S W, Lee J Y, Park W S

机构信息

Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Histopathology. 2008 Apr;52(5):552-9. doi: 10.1111/j.1365-2559.2008.02980.x. Epub 2008 Feb 23.

DOI:10.1111/j.1365-2559.2008.02980.x
PMID:18312352
Abstract

AIMS

alpha-Fetoprotein (AFP) is frequently detected in hepatocellular carcinomas (HCCs) and AT motif binding factor 1 (ATBF1) down-regulates AFP gene expression in hepatic cells. The ATBF1 gene also inhibits cell growth and differentiation, and altered gene expression is associated with malignant transformation. The aim was to investigate the potential role of the ATBF1 gene in HCCs.

METHODS AND RESULTS

Somatic mutations, allelic loss and hypermethylation of the ATBF1 gene were analysed in 76 sporadic HCCs. The level of ATBF-1 mRNA expression was analysed using quantitative real-time reverse transcriptase-polymerase chain reaction. Genetic studies of the ATBF1 gene revealed absence of somatic mutation in the hotspot region and 15 (25%) of 60 informative cases showed allelic loss at the ATBF1 locus. Hypermethylation in the intron 1 region of the ATBF1 gene was detected in only one case. Interestingly, ATBF1 mRNA expression in HCCs was significantly reduced in 55 (72.4%) samples compared with the corresponding surrounding liver tissues. Reduced expression was not statistically associated with clinicopathological parameters including stage, histological grade, infective virus type, and serum alpha-fetoprotein level.

CONCLUSIONS

The ATBF1 gene may contribute to the development of HCCs via transcriptional down-regulation of mRNA expression, but not by genetic or epigenetic alterations.

摘要

目的

甲胎蛋白(AFP)在肝细胞癌(HCC)中常被检测到,而AT基序结合因子1(ATBF1)可下调肝细胞中AFP基因的表达。ATBF1基因还可抑制细胞生长和分化,基因表达改变与恶性转化相关。本研究旨在探讨ATBF1基因在HCC中的潜在作用。

方法与结果

对76例散发性HCC患者的ATBF1基因进行体细胞突变、等位基因缺失和高甲基化分析。采用定量实时逆转录-聚合酶链反应分析ATBF-1 mRNA表达水平。对ATBF1基因的遗传学研究显示,热点区域未发现体细胞突变,60例信息充分的病例中有15例(25%)在ATBF1位点出现等位基因缺失。仅在1例病例中检测到ATBF1基因内含子1区域的高甲基化。有趣的是,与相应的周围肝组织相比,55例(72.4%)HCC样本中ATBF1 mRNA表达显著降低。表达降低与包括分期、组织学分级、感染病毒类型和血清甲胎蛋白水平在内的临床病理参数无统计学关联。

结论

ATBF1基因可能通过转录下调mRNA表达促进HCC的发生发展,而非通过基因或表观遗传改变。

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