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5α-还原酶和17β-羟基类固醇脱氢酶在人前列腺增生和恶性上皮细胞中的表达

5alpha-reductase and 17beta-hydroxysteroid dehydrogenase expression in epithelial cells from hyperplastic and malignant human prostate.

作者信息

Délos S, Carsol J L, Fina F, Raynaud J P, Martin P M

机构信息

Laboratoire de Cancérologie Expérimentale, Faculté de Médecine Nord, Marseille, France.

出版信息

Int J Cancer. 1998 Mar 16;75(6):840-6. doi: 10.1002/(sici)1097-0215(19980316)75:6<840::aid-ijc5>3.0.co;2-v.

Abstract

The aim of this study on testosterone (T) metabolism in benign prostatic hyperplasia (BPH) and prostatic cancer was to compare the formation of metabolites in freshly isolated epithelial cells and in cells of long-term cultures (2 passages) and to identify the 5alpha-reductase (5alpha-R) and 17beta-hydroxysteroid dehydrogenase (17beta-HSD) isoforms responsible for metabolite formation. Androst-4-enedione (A), dihydrotestosterone (DHT) and 5alpha-androstanedione (5alpha-A) formation were measured by high-performance liquid chromatography coupled to a Flo-one HP radioactivity detector. Enzyme isoforms were studied by Northern blot analysis and reverse transcriptase-polymerase chain reaction (RT-PCR). T conversion into A by 17beta-HSD, rather than reduction into DHT by 5alpha-R, was by far the predominant activity in cultured epithelial cells. The metabolic profile did not differ substantially between BPH and cancer cells. Long-term cell culture led to an increase in A formation compared with the level recorded in freshly isolated cells, with no significant incidence on the relative DHT level. According to RT-PCR results, both 5alpha-R isoforms (1 and 2) and 2 17beta-HSD isoforms (2 and 3) are present in epithelial cell cultures and in tissues. According to Northern blot analyses, the mRNAs for 5alpha-R2 and 17beta-HSD4 are expressed in tissue and those for 5alpha-R1 and types 2 and 4 17beta-HSD in isolated cell cultures. Moreover, finasteride, a specific 5alpha-R2 inhibitor, inhibits DHT and 5alpha-A formation in long-term cell culture of adenocarcinoma epithelial cells plated on Matrigel, suggesting a 5alpha-R2 expression. Thus, although 5alpha-R2 is present in freshly isolated epithelial cell cultures and in long-term epithelial cells cultured on Matrigel and predominates in prostate tissue, it is the 5alpha-R1 isoform that is preferentially expressed in epithelial cell cultures.

摘要

本研究旨在比较良性前列腺增生(BPH)和前列腺癌中睾酮(T)的代谢情况,研究新鲜分离的上皮细胞和长期培养(传代2次)细胞中代谢产物的形成,并鉴定负责代谢产物形成的5α-还原酶(5α-R)和17β-羟基类固醇脱氢酶(17β-HSD)同工型。采用高效液相色谱-荧光HP放射性检测器测定雄甾-4-烯二酮(A)、双氢睾酮(DHT)和5α-雄烷二酮(5α-A)的形成。通过Northern印迹分析和逆转录聚合酶链反应(RT-PCR)研究酶同工型。在培养的上皮细胞中,17β-HSD将T转化为A的活性,而非5α-R将T还原为DHT的活性,是迄今为止的主要活性。BPH细胞和癌细胞的代谢谱没有显著差异。与新鲜分离细胞中的水平相比,长期细胞培养导致A形成增加,而相对DHT水平没有显著变化。根据RT-PCR结果,上皮细胞培养物和组织中均存在5α-R的两种同工型(1和2)以及17β-HSD的两种同工型(2和3)。根据Northern印迹分析,5α-R2和17β-HSD4的mRNA在组织中表达,而5α-R1以及17β-HSD的2型和4型的mRNA在分离的细胞培养物中表达。此外,5α-R2特异性抑制剂非那雄胺可抑制接种于基质胶上的腺癌上皮细胞长期培养中的DHT和5α-A形成,提示存在5α-R2表达。因此,尽管5α-R2存在于新鲜分离的上皮细胞培养物以及接种于基质胶上的长期培养上皮细胞中,且在前列腺组织中占主导,但在上皮细胞培养物中优先表达的是5α-R1同工型。

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