Iehlé C, Radvanyi F, Gil Diez de Medina S, Ouafik L H, Gérard H, Chopin D, Raynaud J P, Martin P M
Laboratoire de Cancérologie Expérimentale, INSERM CJF 93-11, Faculté de Médecine Nord, Marseille, France.
J Steroid Biochem Mol Biol. 1999 Mar;68(5-6):189-95. doi: 10.1016/s0960-0760(99)00030-8.
We studied the expression level and cell-specific expression patterns of 5alpha-reductase (5alpha-R) types 1 and 2 iso-enzymes in human hyperplastic and malignant prostate tissue by semi-quantitative RT-PCR and in situ hybridisation analyses. In situ hybridisation established that 5alpha-R1 mRNA is preferentially expressed by epithelial cells and little expressed by stromal cells whereas 5alpha-R2 mRNA is expressed by both epithelium and stroma. Semi-quantitative RT-PCR has been performed on total RNA from different zones of normal prostate, BPH tissues and liver. We found that 5alpha-R1 and 5alpha-R2 mRNAs expression was near the same in all zones of normal prostate. In BPH tissue, 5alpha-R1 and 5alpha-R2 mRNAs expression was slightly but significantly increased, when it was compared to the levels recorded for normal prostate. In cancer samples, 5alpha-R1 mRNA expression was higher than in normal and hyperplastic prostate but the level of 5alpha-R2 mRNA was not statistically different from that observed in the different zones of normal prostate. In liver, 5alpha-R2 mRNA level was similar to that measured in BPH but 5alpha-R1 mRNA expression was ten times higher. The increase observed in 5alpha-R isoenzymes expression in BPH tissue could play an important role in the pathogenesis and/or maintenance of the disease.
我们通过半定量逆转录聚合酶链反应(RT-PCR)和原位杂交分析,研究了5α-还原酶(5α-R)1型和2型同工酶在人前列腺增生组织和恶性前列腺组织中的表达水平及细胞特异性表达模式。原位杂交结果显示,5α-R1 mRNA主要由上皮细胞表达,基质细胞表达较少;而5α-R2 mRNA在上皮和基质中均有表达。我们对来自正常前列腺不同区域、良性前列腺增生(BPH)组织和肝脏的总RNA进行了半定量RT-PCR。我们发现,正常前列腺的所有区域中5α-R1和5α-R2 mRNA的表达水平相近。与正常前列腺相比,BPH组织中5α-R1和5α-R2 mRNA的表达略有增加,但差异显著。在癌症样本中,5α-R1 mRNA的表达高于正常前列腺和增生前列腺,但5α-R2 mRNA的水平与正常前列腺不同区域所观察到的水平无统计学差异。在肝脏中,5α-R2 mRNA水平与BPH组织中测得的水平相似,但5α-R1 mRNA的表达高出十倍。BPH组织中5α-R同工酶表达的增加可能在该疾病的发病机制和/或维持过程中起重要作用。