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
Hauptverfasser: Bisegna, C., Gravina, G. L., Pierconti, F., Martini, M., Larocca, L., Rossi, P., Grimaldi, P., Dolci, S., Di Stasi, S., Jannini, E. A.
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container_end_page 433
container_issue 2
container_start_page 427
container_title Andrology (Oxford)
container_volume 8
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
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L. ; Pierconti, F. ; Martini, M. ; Larocca, L. ; Rossi, P. ; Grimaldi, P. ; Dolci, S. ; Di Stasi, S. ; Jannini, E. A.</creator><creatorcontrib>Bisegna, C. ; Gravina, G. L. ; Pierconti, F. ; Martini, M. ; Larocca, L. ; Rossi, P. ; Grimaldi, P. ; Dolci, S. ; Di Stasi, S. ; Jannini, E. A.</creatorcontrib><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><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. 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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. 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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. 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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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