The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis
Animal models of prostate cancer are essential to identify chemopreventive treatments against this major male malignancy. The N-methyl-N-nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and h...
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Veröffentlicht in: | Toxicologic pathology 2022-06, Vol.50 (4), p.478-496 |
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creator | Bosland, Maarten C. Schlicht, Michael J. Horton, Lori McCormick, David L. |
description | Animal models of prostate cancer are essential to identify chemopreventive treatments against this major male malignancy. The N-methyl-N-nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and has been used extensively in chemoprevention studies with good predictive value for the results of human clinical trials. The objective of this article is to describe the induction protocol of this model, demonstrate its robustness and reproducibility over time and across rat strains, provide diagnostic criteria for the identification of prostate lesions, and present the current tumor induction protocol so that others can use this model in a reliable manner. The majority of accessory sex gland tumors in this model are adenocarcinomas originating in the anterior and dorsolateral prostate that metastasize to lungs and abdominal structures. The rat strain used is of critical importance, with the commercially available Wistar WU and Fischer F344 strains yielding the highest tumor incidences. Low dose, long-term testosterone treatment is essential for a high tumor incidence, but in advanced stage, large adenocarcinomas do not appear to be androgen dependent. This rat model is a robust and reproducible prostate cancer animal model of human prostate cancer. |
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The N-methyl-N-nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and has been used extensively in chemoprevention studies with good predictive value for the results of human clinical trials. The objective of this article is to describe the induction protocol of this model, demonstrate its robustness and reproducibility over time and across rat strains, provide diagnostic criteria for the identification of prostate lesions, and present the current tumor induction protocol so that others can use this model in a reliable manner. The majority of accessory sex gland tumors in this model are adenocarcinomas originating in the anterior and dorsolateral prostate that metastasize to lungs and abdominal structures. The rat strain used is of critical importance, with the commercially available Wistar WU and Fischer F344 strains yielding the highest tumor incidences. Low dose, long-term testosterone treatment is essential for a high tumor incidence, but in advanced stage, large adenocarcinomas do not appear to be androgen dependent. This rat model is a robust and reproducible prostate cancer animal model of human prostate cancer.</description><identifier>ISSN: 0192-6233</identifier><identifier>ISSN: 1533-1601</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1177/01926233221096345</identifier><identifier>PMID: 35588266</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Adenocarcinoma - chemically induced ; Animals ; Carcinogenesis - chemically induced ; Disease Models, Animal ; Humans ; Male ; Prostate ; Prostatic Neoplasms - chemically induced ; Rats ; Rats, Inbred F344 ; Rats, Wistar ; Reproducibility of Results ; Testosterone</subject><ispartof>Toxicologic pathology, 2022-06, Vol.50 (4), p.478-496</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-9ed9052de5989bb0f0178f7fc365454f68e92886955327352ba81511a0d277573</citedby><cites>FETCH-LOGICAL-c438t-9ed9052de5989bb0f0178f7fc365454f68e92886955327352ba81511a0d277573</cites><orcidid>0000-0002-0023-6975</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/01926233221096345$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/01926233221096345$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35588266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bosland, Maarten C.</creatorcontrib><creatorcontrib>Schlicht, Michael J.</creatorcontrib><creatorcontrib>Horton, Lori</creatorcontrib><creatorcontrib>McCormick, David L.</creatorcontrib><title>The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis</title><title>Toxicologic pathology</title><addtitle>Toxicol Pathol</addtitle><description>Animal models of prostate cancer are essential to identify chemopreventive treatments against this major male malignancy. The N-methyl-N-nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and has been used extensively in chemoprevention studies with good predictive value for the results of human clinical trials. The objective of this article is to describe the induction protocol of this model, demonstrate its robustness and reproducibility over time and across rat strains, provide diagnostic criteria for the identification of prostate lesions, and present the current tumor induction protocol so that others can use this model in a reliable manner. The majority of accessory sex gland tumors in this model are adenocarcinomas originating in the anterior and dorsolateral prostate that metastasize to lungs and abdominal structures. The rat strain used is of critical importance, with the commercially available Wistar WU and Fischer F344 strains yielding the highest tumor incidences. Low dose, long-term testosterone treatment is essential for a high tumor incidence, but in advanced stage, large adenocarcinomas do not appear to be androgen dependent. This rat model is a robust and reproducible prostate cancer animal model of human prostate cancer.</description><subject>Adenocarcinoma - chemically induced</subject><subject>Animals</subject><subject>Carcinogenesis - chemically induced</subject><subject>Disease Models, Animal</subject><subject>Humans</subject><subject>Male</subject><subject>Prostate</subject><subject>Prostatic Neoplasms - chemically induced</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Rats, Wistar</subject><subject>Reproducibility of Results</subject><subject>Testosterone</subject><issn>0192-6233</issn><issn>1533-1601</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAQx4Mouj4-gBfp0Us1kzSviyCLL_CF7J5Dtp2ulW6jSSv47c2yuiiCp4HMb_6T-RFyCPQEQKlTCoZJxjljQI3khdggIxCc5yApbJLRsp8vgR2yG-MLpaChoNtkhwuhNZNyRM4mz5jd3U-zx3aI2QRj72OPwXeYPbk-u_MVtpmvs8eQ3l2P2diFsun8HDuMTdwnW7VrIx581T0yvbyYjK_z24erm_H5bV4WXPe5wcpQwSoURpvZjNYUlK5VXXIpClHUUqNhWksjBGeKCzZzGgSAoxVTSii-R85Wua_DbIFViV0fXGtfQ7Nw4cN619jfna55tnP_bg0vFAOZAo6_AoJ_G9KZdtHEEtvWdeiHaJMMpQywQicUVmiZbo4B6_UaoHbp3f7xnmaOfv5vPfEtOgEnKyC6OdoXP4Qu-fon8RP9u4kh</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Bosland, Maarten C.</creator><creator>Schlicht, Michael J.</creator><creator>Horton, Lori</creator><creator>McCormick, David L.</creator><general>SAGE Publications</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0023-6975</orcidid></search><sort><creationdate>20220601</creationdate><title>The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis</title><author>Bosland, Maarten C. ; Schlicht, Michael J. ; Horton, Lori ; McCormick, David L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-9ed9052de5989bb0f0178f7fc365454f68e92886955327352ba81511a0d277573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adenocarcinoma - chemically induced</topic><topic>Animals</topic><topic>Carcinogenesis - chemically induced</topic><topic>Disease Models, Animal</topic><topic>Humans</topic><topic>Male</topic><topic>Prostate</topic><topic>Prostatic Neoplasms - chemically induced</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Rats, Wistar</topic><topic>Reproducibility of Results</topic><topic>Testosterone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bosland, Maarten C.</creatorcontrib><creatorcontrib>Schlicht, Michael J.</creatorcontrib><creatorcontrib>Horton, Lori</creatorcontrib><creatorcontrib>McCormick, David L.</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bosland, Maarten C.</au><au>Schlicht, Michael J.</au><au>Horton, Lori</au><au>McCormick, David L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2022-06-01</date><risdate>2022</risdate><volume>50</volume><issue>4</issue><spage>478</spage><epage>496</epage><pages>478-496</pages><issn>0192-6233</issn><issn>1533-1601</issn><eissn>1533-1601</eissn><abstract>Animal models of prostate cancer are essential to identify chemopreventive treatments against this major male malignancy. The N-methyl-N-nitrosourea (MNU) plus testosterone rat model of prostate carcinogenesis is a reliable animal model that recapitulates human prostate cancer in many respects and has been used extensively in chemoprevention studies with good predictive value for the results of human clinical trials. The objective of this article is to describe the induction protocol of this model, demonstrate its robustness and reproducibility over time and across rat strains, provide diagnostic criteria for the identification of prostate lesions, and present the current tumor induction protocol so that others can use this model in a reliable manner. The majority of accessory sex gland tumors in this model are adenocarcinomas originating in the anterior and dorsolateral prostate that metastasize to lungs and abdominal structures. The rat strain used is of critical importance, with the commercially available Wistar WU and Fischer F344 strains yielding the highest tumor incidences. 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subjects | Adenocarcinoma - chemically induced Animals Carcinogenesis - chemically induced Disease Models, Animal Humans Male Prostate Prostatic Neoplasms - chemically induced Rats Rats, Inbred F344 Rats, Wistar Reproducibility of Results Testosterone |
title | The MNU Plus Testosterone Rat Model of Prostate Carcinogenesis |
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