Down-regulation of dehydroepiandrosterone sulfotransferase gene in human hepatocellular carcinoma

被引:14
|
作者
Huang, LR
Coughtrie, MWH
Hsu, HC
机构
[1] Chungtai Inst Hlth Sci & Technol, Dept Med Technol, Taichung 406, Taiwan
[2] Univ Dundee, Ninewells Hosp & Med Sch, Dept Mol & Cellular Pathol, Dundee DD1 9SY, Scotland
[3] Natl Taiwan Univ, Coll Med, Dept Pathol, Taipei 10018, Taiwan
关键词
dehydroepiandrosterone; dehydroepiandrosterone sulfotransferase (SULT2A1); hepatocellular carcinoma; sex steroids;
D O I
10.1016/j.mce.2004.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Differential display (DD) PCR cloning of differentially expressed genes in hepatocellular carcinoma (HCC) and adjacent unaffected tissue demonstrated preferential down-regulation of a vital sex steroid precursor (dehydroepiandrosterone sulfotransferase; DHEA-ST; SULT2A1) in HCC. SULT2A1 mRNA and/or protein expression in HCC were markedly reduced in 61 of 120 (50.8%) primary unicentric HCCs. The down-regulation was more frequent in grade III versus grade I HCC (68.1% versus 32.1%, P = 0.0025), and in stage 3 versus stage I HCC (62.7% versus 29.2%, P = 0.007). The lowered expression in tumor cells of SULT2A1 in HCC tissues involved in metabolism and/or inactivation of sex steroids is consistent with a regulatory role of the SULT2AI gene product in the development and/or tumor cell differentiation and progression of human HCC. This suggestion is partly supported by our observations that the down-regulated SULT2A1 gene expression correlated with a higher grade and stage of HCC. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
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