Effects of DHT and EGF on human hyperplastic prostate cells cultured in vitro: growth, morphology and phenotype characterisation
This work studies the effects of dihydrotestosterone (DHT) and epidermal growth factor (EGF) on the growth, morphology and phenotype characterisation of the U285 line obtained from human prostate hyperplastic tissue. Modifications of growth rate induced by these two substances have been evaluated by...
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Veröffentlicht in: | Annals of anatomy 1997-06, Vol.179 (3), p.255-264 |
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description | This work studies the effects of dihydrotestosterone (DHT) and epidermal growth factor (EGF) on the growth, morphology and phenotype characterisation of the U285 line obtained from human prostate hyperplastic tissue. Modifications of growth rate induced by these two substances have been evaluated by means of the neutral red assay formulated by Borenfreund and Puerner (1985) as well as by means of Kenacid blue assay described by Knox et al. (1986), culturing cells for 24, 48 and 72 hr with scalar doses of DHT (0.5, 1, 2, 5, 10 μM) and EGF (5, 10, 20, 100 ng/ml). An optical microscope connected to a computer aided system and a scanning electron microscope were used to monitor morphological changes induced by DHT and EGF. The immunophenotype characterisation of the treated and control cells was carried out by using a monoclonal antibody panel. Our results show that the expression of anti-cytokeratin 5+6+18, anticytokeratin 8+18+19 and anti-proline-4-hydroxylase antibodies varied in relation to the type of treatment undergone by the cells. Moreover, exogenous DHT does provoke a flattening of the U285 cells without modifying their rate of growth, while EGF both shortens the lag phase reactivating the quiescent cells and regulates the subsequent log growth phase, thus causing no cellular overgrowth. |
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Modifications of growth rate induced by these two substances have been evaluated by means of the neutral red assay formulated by Borenfreund and Puerner (1985) as well as by means of Kenacid blue assay described by Knox et al. (1986), culturing cells for 24, 48 and 72 hr with scalar doses of DHT (0.5, 1, 2, 5, 10 μM) and EGF (5, 10, 20, 100 ng/ml). An optical microscope connected to a computer aided system and a scanning electron microscope were used to monitor morphological changes induced by DHT and EGF. The immunophenotype characterisation of the treated and control cells was carried out by using a monoclonal antibody panel. Our results show that the expression of anti-cytokeratin 5+6+18, anticytokeratin 8+18+19 and anti-proline-4-hydroxylase antibodies varied in relation to the type of treatment undergone by the cells. Moreover, exogenous DHT does provoke a flattening of the U285 cells without modifying their rate of growth, while EGF both shortens the lag phase reactivating the quiescent cells and regulates the subsequent log growth phase, thus causing no cellular overgrowth.</description><identifier>ISSN: 0940-9602</identifier><identifier>EISSN: 1618-0402</identifier><identifier>DOI: 10.1016/S0940-9602(97)80111-2</identifier><identifier>PMID: 9229079</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Cell Division - drug effects ; Cells, Cultured ; Dihydrotestosterone - pharmacology ; Dose-Response Relationship, Drug ; Epidermal Growth Factor - pharmacology ; Growth assays ; Human hyperplastic cell line ; Humans ; Image analysis ; Immunophenotyping ; Lag phase ; Log phase ; Male ; Microscopy, Electron, Scanning ; Middle Aged ; Prostatic Hyperplasia - pathology ; Scanning electron microscopy</subject><ispartof>Annals of anatomy, 1997-06, Vol.179 (3), p.255-264</ispartof><rights>1997 Gustav Fischer Verlag</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-ce4ed7dbd0ee60a15155e07c8e29d9a56573d3cad3118bce98620eb2bfe8cfc03</citedby><cites>FETCH-LOGICAL-c360t-ce4ed7dbd0ee60a15155e07c8e29d9a56573d3cad3118bce98620eb2bfe8cfc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0940-9602(97)80111-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9229079$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Angeli, Sergio</creatorcontrib><creatorcontrib>Favretti, Cristina</creatorcontrib><creatorcontrib>Buoro, Sabrina</creatorcontrib><creatorcontrib>Fandella, Andrea</creatorcontrib><creatorcontrib>Anselmo, Guiseppe</creatorcontrib><creatorcontrib>Teresa Conconi, Maria</creatorcontrib><creatorcontrib>Paolo Parnigotto, Pier</creatorcontrib><title>Effects of DHT and EGF on human hyperplastic prostate cells cultured in vitro: growth, morphology and phenotype characterisation</title><title>Annals of anatomy</title><addtitle>Ann Anat</addtitle><description>This work studies the effects of dihydrotestosterone (DHT) and epidermal growth factor (EGF) on the growth, morphology and phenotype characterisation of the U285 line obtained from human prostate hyperplastic tissue. Modifications of growth rate induced by these two substances have been evaluated by means of the neutral red assay formulated by Borenfreund and Puerner (1985) as well as by means of Kenacid blue assay described by Knox et al. (1986), culturing cells for 24, 48 and 72 hr with scalar doses of DHT (0.5, 1, 2, 5, 10 μM) and EGF (5, 10, 20, 100 ng/ml). An optical microscope connected to a computer aided system and a scanning electron microscope were used to monitor morphological changes induced by DHT and EGF. The immunophenotype characterisation of the treated and control cells was carried out by using a monoclonal antibody panel. Our results show that the expression of anti-cytokeratin 5+6+18, anticytokeratin 8+18+19 and anti-proline-4-hydroxylase antibodies varied in relation to the type of treatment undergone by the cells. Moreover, exogenous DHT does provoke a flattening of the U285 cells without modifying their rate of growth, while EGF both shortens the lag phase reactivating the quiescent cells and regulates the subsequent log growth phase, thus causing no cellular overgrowth.</description><subject>Cell Division - drug effects</subject><subject>Cells, Cultured</subject><subject>Dihydrotestosterone - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epidermal Growth Factor - pharmacology</subject><subject>Growth assays</subject><subject>Human hyperplastic cell line</subject><subject>Humans</subject><subject>Image analysis</subject><subject>Immunophenotyping</subject><subject>Lag phase</subject><subject>Log phase</subject><subject>Male</subject><subject>Microscopy, Electron, Scanning</subject><subject>Middle Aged</subject><subject>Prostatic Hyperplasia - pathology</subject><subject>Scanning electron microscopy</subject><issn>0940-9602</issn><issn>1618-0402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAQhS0EKpfCI1TyCoFEYOwkTsymQuW2RarEgrK2HHvSGCVxsJ2iu-PR8f1Rt2xmFnPmjM43hFww-MiAiU8_QFZQSAH8nWzet8AYK_gzsmGCtQVUwJ-TzZPkJXkV4y-AUtSiOiNnknMJjdyQv9u-R5Mi9T39entP9Wzp9uaa-pkO66Rz3S0YllHH5Axdgo9JJ6QGxzFSs45pDWipm-mjS8F_pg_B_0nDBzr5sAx-9A-7g-Uy4OxTtqJm0EGbhMFFnZyfX5MXvR4jvjn1c_Lzent_dVvcfb_5dvXlrjClgFQYrNA2trOAKECzmtU1QmNa5NJKXYu6KW1ptC0ZazuDshUcsONdj63pDZTn5O3RN2f4vWJManJxH0PP6NeoGskqIaHMwvooNDlsDNirJbhJh51ioPbk1YG82mNVslEH8ornvYvTgbWb0D5tnVDn-eVxjjnlo8OgonE4G7Qu5A8o691_LvwDNyCV-g</recordid><startdate>19970601</startdate><enddate>19970601</enddate><creator>De Angeli, Sergio</creator><creator>Favretti, Cristina</creator><creator>Buoro, Sabrina</creator><creator>Fandella, Andrea</creator><creator>Anselmo, Guiseppe</creator><creator>Teresa Conconi, Maria</creator><creator>Paolo Parnigotto, Pier</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19970601</creationdate><title>Effects of DHT and EGF on human hyperplastic prostate cells cultured in vitro: growth, morphology and phenotype characterisation</title><author>De Angeli, Sergio ; Favretti, Cristina ; Buoro, Sabrina ; Fandella, Andrea ; Anselmo, Guiseppe ; Teresa Conconi, Maria ; Paolo Parnigotto, Pier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-ce4ed7dbd0ee60a15155e07c8e29d9a56573d3cad3118bce98620eb2bfe8cfc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Cell Division - drug effects</topic><topic>Cells, Cultured</topic><topic>Dihydrotestosterone - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epidermal Growth Factor - pharmacology</topic><topic>Growth assays</topic><topic>Human hyperplastic cell line</topic><topic>Humans</topic><topic>Image analysis</topic><topic>Immunophenotyping</topic><topic>Lag phase</topic><topic>Log phase</topic><topic>Male</topic><topic>Microscopy, Electron, Scanning</topic><topic>Middle Aged</topic><topic>Prostatic Hyperplasia - pathology</topic><topic>Scanning electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Angeli, Sergio</creatorcontrib><creatorcontrib>Favretti, Cristina</creatorcontrib><creatorcontrib>Buoro, Sabrina</creatorcontrib><creatorcontrib>Fandella, Andrea</creatorcontrib><creatorcontrib>Anselmo, Guiseppe</creatorcontrib><creatorcontrib>Teresa Conconi, Maria</creatorcontrib><creatorcontrib>Paolo Parnigotto, Pier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of anatomy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Angeli, Sergio</au><au>Favretti, Cristina</au><au>Buoro, Sabrina</au><au>Fandella, Andrea</au><au>Anselmo, Guiseppe</au><au>Teresa Conconi, Maria</au><au>Paolo Parnigotto, Pier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of DHT and EGF on human hyperplastic prostate cells cultured in vitro: growth, morphology and phenotype characterisation</atitle><jtitle>Annals of anatomy</jtitle><addtitle>Ann Anat</addtitle><date>1997-06-01</date><risdate>1997</risdate><volume>179</volume><issue>3</issue><spage>255</spage><epage>264</epage><pages>255-264</pages><issn>0940-9602</issn><eissn>1618-0402</eissn><abstract>This work studies the effects of dihydrotestosterone (DHT) and epidermal growth factor (EGF) on the growth, morphology and phenotype characterisation of the U285 line obtained from human prostate hyperplastic tissue. Modifications of growth rate induced by these two substances have been evaluated by means of the neutral red assay formulated by Borenfreund and Puerner (1985) as well as by means of Kenacid blue assay described by Knox et al. (1986), culturing cells for 24, 48 and 72 hr with scalar doses of DHT (0.5, 1, 2, 5, 10 μM) and EGF (5, 10, 20, 100 ng/ml). An optical microscope connected to a computer aided system and a scanning electron microscope were used to monitor morphological changes induced by DHT and EGF. The immunophenotype characterisation of the treated and control cells was carried out by using a monoclonal antibody panel. Our results show that the expression of anti-cytokeratin 5+6+18, anticytokeratin 8+18+19 and anti-proline-4-hydroxylase antibodies varied in relation to the type of treatment undergone by the cells. Moreover, exogenous DHT does provoke a flattening of the U285 cells without modifying their rate of growth, while EGF both shortens the lag phase reactivating the quiescent cells and regulates the subsequent log growth phase, thus causing no cellular overgrowth.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>9229079</pmid><doi>10.1016/S0940-9602(97)80111-2</doi><tpages>10</tpages></addata></record> |
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subjects | Cell Division - drug effects Cells, Cultured Dihydrotestosterone - pharmacology Dose-Response Relationship, Drug Epidermal Growth Factor - pharmacology Growth assays Human hyperplastic cell line Humans Image analysis Immunophenotyping Lag phase Log phase Male Microscopy, Electron, Scanning Middle Aged Prostatic Hyperplasia - pathology Scanning electron microscopy |
title | Effects of DHT and EGF on human hyperplastic prostate cells cultured in vitro: growth, morphology and phenotype characterisation |
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