Regulation of PDE5 expression in normal prostate, benign prostatic hyperplasia, and adenocarcinoma
Background Type 5 phosphodiesterase (PDE5) expression in the normal and pathological prostate is controversial. Objectives This study aimed at identifying the cell type/s, if any, expressing PDE5 in human healthy or pathological prostate sections in order to further validate the rationale of PDE5 in...
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Veröffentlicht in: | Andrology (Oxford) 2020-03, Vol.8 (2), p.427-433 |
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creator | Bisegna, C. Gravina, G. L. Pierconti, F. Martini, M. Larocca, L. Rossi, P. Grimaldi, P. Dolci, S. Di Stasi, S. Jannini, E. A. |
description | Background
Type 5 phosphodiesterase (PDE5) expression in the normal and pathological prostate is controversial.
Objectives
This study aimed at identifying the cell type/s, if any, expressing PDE5 in human healthy or pathological prostate sections in order to further validate the rationale of PDE5 inhibitor (PDE5i) treatment of benign prostatic hyperplasia (BPH) and their safety in the treatment of erectile dysfunction following prostate cancer (PCa) surgery.
Materials and methods
By immunohistochemical analysis, we studied PDE5 expression in tissue microarrays containing sections obtained from healthy, BPH, and PCa samples.
Results
Our results showed that PDE5 is barely expressed in the epithelial or stromal compartment of normal human prostates, but it is highly expressed in the stromal compartment of BPH sections. We also found that a low but significant number of PCa samples (22%) expressed PDE5 in the epithelial cancer cells but not in stromal cells and that such expression was not correlated with the tumor aggressiveness, according to their Gleason score.
Discussion and conclusion
PDE5 overexpression in the stromal compartment of BPH samples supports the rationale of PDE5 as a target in lower urinary tract symptoms of BPH. PDE5 expression in a significant percentage of PCa samples but the lack of correlation with the Gleason score suggests that this enzyme is not correlated with tumor aggressiveness; however, a role of PDE5 in the minimal residual disease of PCa cannot be excluded. |
doi_str_mv | 10.1111/andr.12695 |
format | Article |
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Type 5 phosphodiesterase (PDE5) expression in the normal and pathological prostate is controversial.
Objectives
This study aimed at identifying the cell type/s, if any, expressing PDE5 in human healthy or pathological prostate sections in order to further validate the rationale of PDE5 inhibitor (PDE5i) treatment of benign prostatic hyperplasia (BPH) and their safety in the treatment of erectile dysfunction following prostate cancer (PCa) surgery.
Materials and methods
By immunohistochemical analysis, we studied PDE5 expression in tissue microarrays containing sections obtained from healthy, BPH, and PCa samples.
Results
Our results showed that PDE5 is barely expressed in the epithelial or stromal compartment of normal human prostates, but it is highly expressed in the stromal compartment of BPH sections. We also found that a low but significant number of PCa samples (22%) expressed PDE5 in the epithelial cancer cells but not in stromal cells and that such expression was not correlated with the tumor aggressiveness, according to their Gleason score.
Discussion and conclusion
PDE5 overexpression in the stromal compartment of BPH samples supports the rationale of PDE5 as a target in lower urinary tract symptoms of BPH. PDE5 expression in a significant percentage of PCa samples but the lack of correlation with the Gleason score suggests that this enzyme is not correlated with tumor aggressiveness; however, a role of PDE5 in the minimal residual disease of PCa cannot be excluded.</description><identifier>ISSN: 2047-2919</identifier><identifier>EISSN: 2047-2927</identifier><identifier>DOI: 10.1111/andr.12695</identifier><identifier>PMID: 31433119</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adenocarcinoma - enzymology ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Cancer ; Cyclic Nucleotide Phosphodiesterases, Type 5 - analysis ; Cyclic Nucleotide Phosphodiesterases, Type 5 - biosynthesis ; Erectile dysfunction ; Genital diseases ; Human ; Humans ; Hyperplasia ; Immunohistochemistry ; Male ; Middle Aged ; Pathology ; PDE5 inhibitor ; Phosphodiesterase ; Prostate ; Prostate - enzymology ; Prostate - pathology ; Prostate cancer ; Prostatic Hyperplasia - enzymology ; Prostatic Hyperplasia - pathology ; Prostatic Neoplasms - enzymology ; Prostatic Neoplasms - pathology ; Sexual disorders ; Young Adult</subject><ispartof>Andrology (Oxford), 2020-03, Vol.8 (2), p.427-433</ispartof><rights>2019 American Society of Andrology and European Academy of Andrology</rights><rights>2019 American Society of Andrology and European Academy of Andrology.</rights><rights>Andrology © 2020 American Society of Andrology and European Academy of Andrology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5874-039X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fandr.12695$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fandr.12695$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31433119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bisegna, C.</creatorcontrib><creatorcontrib>Gravina, G. L.</creatorcontrib><creatorcontrib>Pierconti, F.</creatorcontrib><creatorcontrib>Martini, M.</creatorcontrib><creatorcontrib>Larocca, L.</creatorcontrib><creatorcontrib>Rossi, P.</creatorcontrib><creatorcontrib>Grimaldi, P.</creatorcontrib><creatorcontrib>Dolci, S.</creatorcontrib><creatorcontrib>Di Stasi, S.</creatorcontrib><creatorcontrib>Jannini, E. A.</creatorcontrib><title>Regulation of PDE5 expression in normal prostate, benign prostatic hyperplasia, and adenocarcinoma</title><title>Andrology (Oxford)</title><addtitle>Andrology</addtitle><description>Background
Type 5 phosphodiesterase (PDE5) expression in the normal and pathological prostate is controversial.
Objectives
This study aimed at identifying the cell type/s, if any, expressing PDE5 in human healthy or pathological prostate sections in order to further validate the rationale of PDE5 inhibitor (PDE5i) treatment of benign prostatic hyperplasia (BPH) and their safety in the treatment of erectile dysfunction following prostate cancer (PCa) surgery.
Materials and methods
By immunohistochemical analysis, we studied PDE5 expression in tissue microarrays containing sections obtained from healthy, BPH, and PCa samples.
Results
Our results showed that PDE5 is barely expressed in the epithelial or stromal compartment of normal human prostates, but it is highly expressed in the stromal compartment of BPH sections. We also found that a low but significant number of PCa samples (22%) expressed PDE5 in the epithelial cancer cells but not in stromal cells and that such expression was not correlated with the tumor aggressiveness, according to their Gleason score.
Discussion and conclusion
PDE5 overexpression in the stromal compartment of BPH samples supports the rationale of PDE5 as a target in lower urinary tract symptoms of BPH. PDE5 expression in a significant percentage of PCa samples but the lack of correlation with the Gleason score suggests that this enzyme is not correlated with tumor aggressiveness; however, a role of PDE5 in the minimal residual disease of PCa cannot be excluded.</description><subject>Adenocarcinoma - enzymology</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer</subject><subject>Cyclic Nucleotide Phosphodiesterases, Type 5 - analysis</subject><subject>Cyclic Nucleotide Phosphodiesterases, Type 5 - biosynthesis</subject><subject>Erectile dysfunction</subject><subject>Genital diseases</subject><subject>Human</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pathology</subject><subject>PDE5 inhibitor</subject><subject>Phosphodiesterase</subject><subject>Prostate</subject><subject>Prostate - enzymology</subject><subject>Prostate - pathology</subject><subject>Prostate cancer</subject><subject>Prostatic Hyperplasia - enzymology</subject><subject>Prostatic Hyperplasia - pathology</subject><subject>Prostatic Neoplasms - enzymology</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Sexual disorders</subject><subject>Young Adult</subject><issn>2047-2919</issn><issn>2047-2927</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1LxEAMhgdRVNSLP0AGvHhwdb7HOYrrF4jKoueStqmOtNM6s0X33zvrqgdDICF5CC95Cdnn7ITnOIVQxxMujNNrZFswZSfCCbv-13O3RfZSemM5zpYpNsmW5EpKzt02KWf4MrYw932gfUMfp5ea4ucQMaXlyAca-thBS4fYpznM8ZiWGPxL-B34ir4uBoxDC8nDMc16KNQY-gpi5UPfwS7ZaKBNuPdTd8jz1eXTxc3k7uH69uL8bjJIbvVEMQNZHjCF5ZmtmXZoG1cZocCx0grDBbC6hlJbVYKRCLYqLbrGGN2AMXKHHK3uZmXvI6Z50flUYdtCwH5MhZBSc6u0FBk9_Ie-9WMMWV2mjLPKKKYzdfBDjWWHdTFE30FcFL_fywBfAR--xcXfnrNiaU2xtKb4tqY4v5_Ovjv5BXmLgIM</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Bisegna, C.</creator><creator>Gravina, G. L.</creator><creator>Pierconti, F.</creator><creator>Martini, M.</creator><creator>Larocca, L.</creator><creator>Rossi, P.</creator><creator>Grimaldi, P.</creator><creator>Dolci, S.</creator><creator>Di Stasi, S.</creator><creator>Jannini, E. A.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5874-039X</orcidid></search><sort><creationdate>202003</creationdate><title>Regulation of PDE5 expression in normal prostate, benign prostatic hyperplasia, and adenocarcinoma</title><author>Bisegna, C. ; Gravina, G. L. ; Pierconti, F. ; Martini, M. ; Larocca, L. ; Rossi, P. ; Grimaldi, P. ; Dolci, S. ; Di Stasi, S. ; Jannini, E. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3175-406a080a04eb87d059e7f9c624a90b72612a0ddab574ba63ea7cb7e9f665fa663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adenocarcinoma - enzymology</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer</topic><topic>Cyclic Nucleotide Phosphodiesterases, Type 5 - analysis</topic><topic>Cyclic Nucleotide Phosphodiesterases, Type 5 - biosynthesis</topic><topic>Erectile dysfunction</topic><topic>Genital diseases</topic><topic>Human</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pathology</topic><topic>PDE5 inhibitor</topic><topic>Phosphodiesterase</topic><topic>Prostate</topic><topic>Prostate - enzymology</topic><topic>Prostate - pathology</topic><topic>Prostate cancer</topic><topic>Prostatic Hyperplasia - enzymology</topic><topic>Prostatic Hyperplasia - pathology</topic><topic>Prostatic Neoplasms - enzymology</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Sexual disorders</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bisegna, C.</creatorcontrib><creatorcontrib>Gravina, G. L.</creatorcontrib><creatorcontrib>Pierconti, F.</creatorcontrib><creatorcontrib>Martini, M.</creatorcontrib><creatorcontrib>Larocca, L.</creatorcontrib><creatorcontrib>Rossi, P.</creatorcontrib><creatorcontrib>Grimaldi, P.</creatorcontrib><creatorcontrib>Dolci, S.</creatorcontrib><creatorcontrib>Di Stasi, S.</creatorcontrib><creatorcontrib>Jannini, E. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Andrology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bisegna, C.</au><au>Gravina, G. L.</au><au>Pierconti, F.</au><au>Martini, M.</au><au>Larocca, L.</au><au>Rossi, P.</au><au>Grimaldi, P.</au><au>Dolci, S.</au><au>Di Stasi, S.</au><au>Jannini, E. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of PDE5 expression in normal prostate, benign prostatic hyperplasia, and adenocarcinoma</atitle><jtitle>Andrology (Oxford)</jtitle><addtitle>Andrology</addtitle><date>2020-03</date><risdate>2020</risdate><volume>8</volume><issue>2</issue><spage>427</spage><epage>433</epage><pages>427-433</pages><issn>2047-2919</issn><eissn>2047-2927</eissn><abstract>Background
Type 5 phosphodiesterase (PDE5) expression in the normal and pathological prostate is controversial.
Objectives
This study aimed at identifying the cell type/s, if any, expressing PDE5 in human healthy or pathological prostate sections in order to further validate the rationale of PDE5 inhibitor (PDE5i) treatment of benign prostatic hyperplasia (BPH) and their safety in the treatment of erectile dysfunction following prostate cancer (PCa) surgery.
Materials and methods
By immunohistochemical analysis, we studied PDE5 expression in tissue microarrays containing sections obtained from healthy, BPH, and PCa samples.
Results
Our results showed that PDE5 is barely expressed in the epithelial or stromal compartment of normal human prostates, but it is highly expressed in the stromal compartment of BPH sections. We also found that a low but significant number of PCa samples (22%) expressed PDE5 in the epithelial cancer cells but not in stromal cells and that such expression was not correlated with the tumor aggressiveness, according to their Gleason score.
Discussion and conclusion
PDE5 overexpression in the stromal compartment of BPH samples supports the rationale of PDE5 as a target in lower urinary tract symptoms of BPH. PDE5 expression in a significant percentage of PCa samples but the lack of correlation with the Gleason score suggests that this enzyme is not correlated with tumor aggressiveness; however, a role of PDE5 in the minimal residual disease of PCa cannot be excluded.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31433119</pmid><doi>10.1111/andr.12695</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5874-039X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - enzymology Adenocarcinoma - pathology Adult Aged Aged, 80 and over Cancer Cyclic Nucleotide Phosphodiesterases, Type 5 - analysis Cyclic Nucleotide Phosphodiesterases, Type 5 - biosynthesis Erectile dysfunction Genital diseases Human Humans Hyperplasia Immunohistochemistry Male Middle Aged Pathology PDE5 inhibitor Phosphodiesterase Prostate Prostate - enzymology Prostate - pathology Prostate cancer Prostatic Hyperplasia - enzymology Prostatic Hyperplasia - pathology Prostatic Neoplasms - enzymology Prostatic Neoplasms - pathology Sexual disorders Young Adult |
title | Regulation of PDE5 expression in normal prostate, benign prostatic hyperplasia, and adenocarcinoma |
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