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类固醇激素和生长因子刺激下增生前列腺中前列腺酸性磷酸酶和前列腺特异性抗原mRNA水平的比较分析

Comparative analysis of prostatic acid phosphatase and prostate-specific antigen mRNA levels in hyperplastic prostate stimulated with steroid hormones and growth factors.

作者信息

Dulińska Joanna, Laidler Piotr, Labedź Maria

机构信息

Institute of Medical Biochemistry, Medical College, Jagiellonian University, Kraków, Poland.

出版信息

Acta Biochim Pol. 2002;49(2):357-68.

Abstract

Prostatic acid phosphatase (PAP) and prostate-specific antigen (PSA) are the markers of human prostatic gland. However, it is still not completely understood if and how, steroid hormones and growth factors affect their expression and metabolism in the respect to the major pathologies of the gland. Appropriate studies were carried out on histopathologically diagnosed benign prostatic hyperplasia--BPH (n = 42) using tissue slices and cells derived from them. They were incubated with steroid hormones: 5-alpha-dihydrotestosterone (DHT), estradiol (E) and growth factors: epidermal growth factor (EGF), basic fibroblastic growth factor (bFGF) under culture conditions for up to 24 hours. P-labelled specific oligonucleotide probes were used to analyze total RNA isolated from each sample for the presence of PAP and PSA mRNAs. DHT, E, bFGF, EGF or both DHT + bFGF and DHT + EGF increased PAP and PSA mRNA levels in a time- and dose-dependent manner. The highest and statistically significant increase (P < 0.001) for PAP mRNA was observed when DHT + bFGF were present in the medium while for PSA mRNA if DHT + EGF were added to the medium. Slow but constant decrease of PAP and PSA mRNA levels was observed in the absence of each of these factors in the incubation medium. The results suggest that early expression of PSA and PAP genes and/or their mRNA stability strongly depend on DHT while differ in their response to EGF and bFGF.

摘要

前列腺酸性磷酸酶(PAP)和前列腺特异性抗原(PSA)是人类前列腺的标志物。然而,类固醇激素和生长因子是否以及如何影响它们在前列腺主要病理方面的表达和代谢,目前仍未完全明确。我们对经组织病理学诊断为良性前列腺增生(BPH,n = 42)的患者进行了适当研究,使用组织切片及其衍生的细胞。将它们在培养条件下与类固醇激素:5-α-双氢睾酮(DHT)、雌二醇(E)以及生长因子:表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)一起孵育长达24小时。使用P标记的特异性寡核苷酸探针分析从每个样本中分离的总RNA中PAP和PSA mRNA的存在情况。DHT、E、bFGF、EGF或DHT + bFGF以及DHT + EGF均以时间和剂量依赖性方式增加PAP和PSA mRNA水平。当培养基中存在DHT + bFGF时,观察到PAP mRNA出现最高且具有统计学显著性的增加(P < 0.001),而当向培养基中添加DHT + EGF时,PSA mRNA出现这种情况。在孵育培养基中缺乏这些因素中的任何一种时,观察到PAP和PSA mRNA水平缓慢但持续下降。结果表明,PSA和PAP基因的早期表达和/或它们的mRNA稳定性强烈依赖于DHT,而它们对EGF和bFGF的反应有所不同。

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