Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9369
Title: Localization of angiotensin-converting enzyme in the human prostate: pathological expression in benign prostatic hyperplasia.
Authors: Nassis, L;Frauman, Albert G;Ohishi, M;Zhuo, J;Casley, David J;Johnston, Colin I;Fabiani, Mark E
Affiliation: Department of Medicine, University of Melbourne, Austin and Repatriation Medical Centre, Heidelberg, VIC 3084, Australia.
Issue Date: 1-Dec-2001
Citation: The Journal of Pathology; 195(5): 571-9
Abstract: Benign prostatic hyperplasia (BPH) is the most common hyperplastic disease in man and it is characterized by increased cellular growth (stromal and epithelial hyperplasia) and enhanced local sympathetic tone, both of which are known to be augmented by activation of the renin-angiotensin system (RAS) in other tissues. Angiotensin-converting enzyme (ACE) is an integral component of the RAS that is responsible for the production of the active peptide angiotensin II from the inactive precursor angiotensin I. The present study was undertaken to map the anatomical localization of ACE protein and messenger ribonucleic acid (mRNA) in the normal human prostate and to establish whether their expression is pathologically altered in BPH. Human prostate samples were obtained at post-mortem and histologically defined as normal or hyperplastic. ACE protein binding/expression was determined by in vitro autoradiography and immunohistochemistry using the ACE-specific radioligand [125I]-MK351A and a mouse anti-ACE polyclonal antibody, respectively, whereas the spatiotemporal distribution of ACE mRNA was determined by in situ hybridization using 35S-labelled oligonucleotide probes. ACE protein was localized to the glandular epithelium in the human prostate. ACE binding and immunostaining were increased in BPH compared with normal (non-hyperplastic) prostate specimens [X-ray film autoradiography: normal 873+/-48 dpm/mm2 (n=8) vs. BPH 1631+/-274 dpm/mm2 (n=6), p<0.05; emulsion autoradiography: normal 3.1+/-0.5 grains/mm2 (n=6) vs. BPH 32.8+/-8.6 grains/mm2 (n=5), p<0.01]. ACE mRNA was also localized to glandular epithelial cells in the human prostate with a significant increase in ACE mRNA expression in BPH compared with the normal prostate [normal 11.04+/-2.03 grains/cell (n=220 cells total) vs. BPH 22.29+/-1.34 grains/cell (n=198 cells total), p<0.05]. The findings of the present study suggest that ACE is localized to the glandular epithelium of the human prostate and that its expression, at both protein and mRNA level, is aberrantly increased in BPH. These data support the concept that hyperactivity of the local RAS in the prostate may be involved in the pathogenesis of BPH.
Internal ID Number: 11745693
URI: http://ahro.austin.org.au/austinjspui/handle/1/9369
DOI: 10.1002/path.999
URL: http://www.ncbi.nlm.nih.gov/pubmed/11745693
Type: Journal Article
Subjects: Autoradiography
Gene Expression
Humans
Immunoenzyme Techniques
In Situ Hybridization
Male
Middle Aged
Peptidyl-Dipeptidase A.genetics.metabolism
Prostate.enzymology
Prostatic Hyperplasia.enzymology
RNA, Messenger.genetics
Appears in Collections:Journal articles

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