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前列腺癌中膜睾酮结合位点作为一种潜在的新标志物和治疗靶点:石蜡组织切片研究

Membrane testosterone binding sites in prostate carcinoma as a potential new marker and therapeutic target: study in paraffin tissue sections.

作者信息

Dambaki Constantina, Kogia Christina, Kampa Marilena, Darivianaki Katherine, Nomikos Michael, Anezinis Ploutarchos, Theodoropoulos Panayiotis A, Castanas Elias, Stathopoulos Efstathios N

机构信息

Department of Pathology, University of Crete, School of Medicine, Heraklion, Greece.

出版信息

BMC Cancer. 2005 Nov 17;5:148. doi: 10.1186/1471-2407-5-148.

Abstract

BACKGROUND

Steroid action is mediated, in addition to classical intracellular receptors, by recently identified membrane sites, that generate rapid non-genomic effects. We have recently identified a membrane androgen receptor site on prostate carcinoma cells, mediating testosterone rapid effects on the cytoskeleton and secretion within minutes.

METHODS

The aim of this study was to investigate whether membrane androgen receptors are differentially expressed in prostate carcinomas, and their relationship to the tumor grade. We examined the expression of membrane androgen receptors in archival material of 109 prostate carcinomas and 103 benign prostate hyperplasias, using fluorescein-labeled BSA-coupled testosterone.

RESULTS

We report that membrane androgen receptors are preferentially expressed in prostate carcinomas, and they correlate to their grade using the Gleason's microscopic grading score system.

CONCLUSION

We conclude that membrane androgen receptors may represent an index of tumor aggressiveness and possibly specific targets for new therapeutic regimens.

摘要

背景

除了经典的细胞内受体外,类固醇作用还可通过最近发现的膜位点介导,这些位点可产生快速的非基因组效应。我们最近在前列腺癌细胞上鉴定出一个膜雄激素受体位点,该位点可在数分钟内介导睾酮对细胞骨架和分泌的快速作用。

方法

本研究的目的是调查膜雄激素受体在前列腺癌中是否存在差异表达,以及它们与肿瘤分级的关系。我们使用荧光素标记的牛血清白蛋白偶联睾酮,检测了109例前列腺癌和103例良性前列腺增生存档材料中膜雄激素受体的表达。

结果

我们报告膜雄激素受体在前列腺癌中优先表达,并且使用 Gleason 显微镜分级评分系统,它们与肿瘤分级相关。

结论

我们得出结论,膜雄激素受体可能代表肿瘤侵袭性的一个指标,并且可能是新治疗方案的特定靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24bd/1318463/8f15c0da1fd7/1471-2407-5-148-1.jpg

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