17β-Hydroxysteroid dehydrogenase Type 1 and Type 2:: Association between mRNA expression and activity in cell lines

被引:30
作者
Day, JM
Tutill, HJ
Newman, SP
Purohit, A
Lawrence, HR
Vicker, N
Potter, BVL
Reed, MJ
机构
[1] St Marys Hosp, Dept Endocrinol & Metab Med, Sterix Ltd, Imperial Coll, London W2 1NY, England
[2] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[3] Univ Bath, Sterix Ltd, Bath BA2 7AY, Avon, England
关键词
17 beta-hydroxysteroid dehydrogenase; HSD; type; 1; 2; breast cancer;
D O I
10.1016/j.mce.2006.01.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
17 beta-Hydroxysteroid dehydrogenases (17 beta-HSDs) are a family of enzymes that regulate steroid availability within a tissue by catalysing the interconversion of active and inactive forms. Type 1 is up-regulated in many breast tumours, and is responsible for the reduction of oestrone to active oestradiol which stimulates cell proliferation within the tumour. Type 2 oxidises many active steroids to their inactive forms, including oestradiol to oestrone. In this study, we have compared the mRNA expression and enzyme activities of Type 1 and Type 2 in MCF-7, MDA-MB-231, T47D, JEG3 and 293-EBNA cell lines. Also studied were two cell lines stably expressing transfected Type I cDNA. RT-PCR indicated that little Type I mRNA is expressed in two of the breast cancer cell lines, MCF-7 and MDA-MB-231, and in 293-EBNA cells, but that expression is much higher in the T47D breast cancer cell line, and in the choriocarcinoma cell line, JEG3. However, a higher level of expression of Type I is seen in the transfected cell lines MCF-7.8H and 293-EBNA[His(6)17 beta-HSD1]. Activity assays show that there is high association between mRNA expression and enzyme activity. Assays indicate that, with the exception of MDA-MB-231 cells, Type 2 activity is low in these lines. The study of the basal activities of these enzymes will be used in future studies investigating the regulation of the enzymes by endogenous and exogenous factors. An understanding of their regulation in both healthy and malignant tissues may lead to future therapeutic intervention at the regulatory level. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:246 / 249
页数:4
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