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首页> 外文期刊>Molecular and Cellular Endocrinology >17beta-Hydroxysteroid dehydrogenase Type 1 and Type 2: Association between mRNA expression and activity in cell lines.
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17beta-Hydroxysteroid dehydrogenase Type 1 and Type 2: Association between mRNA expression and activity in cell lines.

机译:17beta-羟基类固醇脱氢酶1型和2型:mRNA表达与细胞系活性之间的关联。

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17beta-Hydroxysteroid dehydrogenases (17beta-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 1 cDNA. RT-PCR indicated that little Type 1 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 1 is seen in the transfected cell lines MCF-7.8H and 293-EBNA[His(6)17beta-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.
机译:17beta-羟基类固醇脱氢酶(17beta-HSDs)是一类酶,它们通过催化活性形式和非活性形式的相互转化来调节组织中类固醇的利用率。 1型在许多乳腺肿瘤中上调,并导致雌酮减少为活性雌二醇,从而刺激肿瘤内的细胞增殖。 2型将许多活性类固醇氧化为非活性形式,包括雌二醇为雌酮。在这项研究中,我们比较了MCF-7,MDA-MB-231,T47D,JEG3和293-EBNA细胞系中1型和2型的mRNA表达和酶活性。还研究了稳定表达转染的1型cDNA的两种细胞系。 RT-PCR表明,两种乳腺癌细胞系MCF-7和MDA-MB-231和293-EBNA细胞中几乎没有1型mRNA的表达,但在T47D乳腺癌细胞系中的表达要高得多。 ,以及绒毛膜癌细胞系JEG3。但是,在转染的细胞系MCF-7.8H和293-EBNA [His(6)17beta-HSD1]中看到了更高水平的1型表达。活性分析表明,mRNA表达与酶活性之间存在高度关联。测定表明,除了MDA-MB-231细胞外,这些细胞系中的2型活性低。这些酶的基础活性的研究将用于未来的研究中,以研究内源性和外源性因素对酶的调节作用。对它们在健康和恶性组织中的调节的理解可能导致将来在调节水平上的治疗干预。

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