Inhibin B as a potential biomarker of testicular toxicity
Inhibin B is a glycoprotein produced predominantly by Sertoli cells which regulates pituitary FSH release by a negative feedback loop. The regulation of inhibin B is complex with changes in the pattern of secretion occurring during development, and many factors such as FSH, testosterone, Sertoli cel...
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Veröffentlicht in: | Cancer biomarkers : section A of Disease markers 2005, Vol.1 (1), p.75-91 |
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description | Inhibin B is a glycoprotein produced predominantly by Sertoli cells which regulates pituitary FSH release by a negative feedback loop. The regulation of inhibin B is complex with changes in the pattern of secretion occurring during development, and many factors such as FSH, testosterone, Sertoli cell proliferation and germ cell complement likely to contribute to overall production. Systemic inhibin B concentrations seem to reflect the extreme ends of spermatogenic status with high levels of inhibin B observed in normal, fertile individuals and lower levels of inhibin B in individuals with severe damage to the testis as a result of germ cell depletion. Inhibin B has proved valuable in epidemiological studies exploring male infertility with data showing that inhibin B combined with FSH measurements has a higher positive predictive value for detecting male infertility than either alone. Inhibin B is proposed as a potential biomarker of testicular toxicity in rodent toxicity studies to compliment traditional endpoints. In pharmaceutical development, inhibin B might allow better linkage between animal study results and subsequent monitoring of testicular function in clinical trials. An international, intercompany project has been initiated to evaluate the overall suitability and limitations of inhibin B as a biomarker of testicular toxicity. |
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The regulation of inhibin B is complex with changes in the pattern of secretion occurring during development, and many factors such as FSH, testosterone, Sertoli cell proliferation and germ cell complement likely to contribute to overall production. Systemic inhibin B concentrations seem to reflect the extreme ends of spermatogenic status with high levels of inhibin B observed in normal, fertile individuals and lower levels of inhibin B in individuals with severe damage to the testis as a result of germ cell depletion. Inhibin B has proved valuable in epidemiological studies exploring male infertility with data showing that inhibin B combined with FSH measurements has a higher positive predictive value for detecting male infertility than either alone. Inhibin B is proposed as a potential biomarker of testicular toxicity in rodent toxicity studies to compliment traditional endpoints. In pharmaceutical development, inhibin B might allow better linkage between animal study results and subsequent monitoring of testicular function in clinical trials. An international, intercompany project has been initiated to evaluate the overall suitability and limitations of inhibin B as a biomarker of testicular toxicity.</description><identifier>ISSN: 1574-0153</identifier><identifier>EISSN: 1875-8592</identifier><identifier>DOI: 10.3233/CBM-2005-1109</identifier><identifier>PMID: 17192034</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Adult ; Animals ; Biomarkers - analysis ; Drug-Related Side Effects and Adverse Reactions - diagnosis ; Humans ; Inhibins - analysis ; Inhibins - biosynthesis ; Inhibins - chemistry ; Inhibins - physiology ; Male ; Models, Biological ; Rodentia ; Spermatogenesis - physiology ; Testicular Diseases - chemically induced ; Testis - drug effects ; Testis - growth & development ; Testis - metabolism</subject><ispartof>Cancer biomarkers : section A of Disease markers, 2005, Vol.1 (1), p.75-91</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c238t-b46db94b7fb03cb1c85a029192ffcf1125f6b65617b8ad48eed268cd8c391d693</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17192034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Dixit, Rakesh</contributor><creatorcontrib>Stewart, Jane</creatorcontrib><creatorcontrib>Turner, Katie J</creatorcontrib><title>Inhibin B as a potential biomarker of testicular toxicity</title><title>Cancer biomarkers : section A of Disease markers</title><addtitle>Cancer Biomark</addtitle><description>Inhibin B is a glycoprotein produced predominantly by Sertoli cells which regulates pituitary FSH release by a negative feedback loop. The regulation of inhibin B is complex with changes in the pattern of secretion occurring during development, and many factors such as FSH, testosterone, Sertoli cell proliferation and germ cell complement likely to contribute to overall production. Systemic inhibin B concentrations seem to reflect the extreme ends of spermatogenic status with high levels of inhibin B observed in normal, fertile individuals and lower levels of inhibin B in individuals with severe damage to the testis as a result of germ cell depletion. Inhibin B has proved valuable in epidemiological studies exploring male infertility with data showing that inhibin B combined with FSH measurements has a higher positive predictive value for detecting male infertility than either alone. Inhibin B is proposed as a potential biomarker of testicular toxicity in rodent toxicity studies to compliment traditional endpoints. In pharmaceutical development, inhibin B might allow better linkage between animal study results and subsequent monitoring of testicular function in clinical trials. An international, intercompany project has been initiated to evaluate the overall suitability and limitations of inhibin B as a biomarker of testicular toxicity.</description><subject>Adult</subject><subject>Animals</subject><subject>Biomarkers - analysis</subject><subject>Drug-Related Side Effects and Adverse Reactions - diagnosis</subject><subject>Humans</subject><subject>Inhibins - analysis</subject><subject>Inhibins - biosynthesis</subject><subject>Inhibins - chemistry</subject><subject>Inhibins - physiology</subject><subject>Male</subject><subject>Models, Biological</subject><subject>Rodentia</subject><subject>Spermatogenesis - physiology</subject><subject>Testicular Diseases - chemically induced</subject><subject>Testis - drug effects</subject><subject>Testis - growth & development</subject><subject>Testis - metabolism</subject><issn>1574-0153</issn><issn>1875-8592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkDtPwzAURi0EoqUwsiJvTAa_Y4-04lGpiAVmy3ZsYUiTEicS_fc4aiWme4ej77v3AHBN8B2jjN2vlq-IYiwQIVifgDlRlUBKaHpadlFxhIlgM3CR8xfGnBGqz8GMVERTzPgc6HX7mVxq4RLaDC3cdUNoh2Qb6FK3tf136GEX4RDykPzY2B4O3W_yadhfgrNomxyujnMBPp4e31cvaPP2vF49bJCnTA3IcVk7zV0VHWbeEa-ExVSX_hh9JISKKJ0UklRO2ZqrEGoqla-VZ5rUUrMFuD3k7vruZyx3mG3KPjSNbUM3ZlNxIRmrKC8kOpC-73LuQzS7PpUf9oZgM8kyRZaZZJlJVuFvjsmj24b6nz7aYX_LHGPI</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>Stewart, Jane</creator><creator>Turner, Katie J</creator><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>2005</creationdate><title>Inhibin B as a potential biomarker of testicular toxicity</title><author>Stewart, Jane ; Turner, Katie J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c238t-b46db94b7fb03cb1c85a029192ffcf1125f6b65617b8ad48eed268cd8c391d693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Biomarkers - analysis</topic><topic>Drug-Related Side Effects and Adverse Reactions - diagnosis</topic><topic>Humans</topic><topic>Inhibins - analysis</topic><topic>Inhibins - biosynthesis</topic><topic>Inhibins - chemistry</topic><topic>Inhibins - physiology</topic><topic>Male</topic><topic>Models, Biological</topic><topic>Rodentia</topic><topic>Spermatogenesis - physiology</topic><topic>Testicular Diseases - chemically induced</topic><topic>Testis - drug effects</topic><topic>Testis - growth & development</topic><topic>Testis - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stewart, Jane</creatorcontrib><creatorcontrib>Turner, Katie J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Cancer biomarkers : section A of Disease markers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stewart, Jane</au><au>Turner, Katie J</au><au>Dixit, Rakesh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibin B as a potential biomarker of testicular toxicity</atitle><jtitle>Cancer biomarkers : section A of Disease markers</jtitle><addtitle>Cancer Biomark</addtitle><date>2005</date><risdate>2005</risdate><volume>1</volume><issue>1</issue><spage>75</spage><epage>91</epage><pages>75-91</pages><issn>1574-0153</issn><eissn>1875-8592</eissn><abstract>Inhibin B is a glycoprotein produced predominantly by Sertoli cells which regulates pituitary FSH release by a negative feedback loop. The regulation of inhibin B is complex with changes in the pattern of secretion occurring during development, and many factors such as FSH, testosterone, Sertoli cell proliferation and germ cell complement likely to contribute to overall production. Systemic inhibin B concentrations seem to reflect the extreme ends of spermatogenic status with high levels of inhibin B observed in normal, fertile individuals and lower levels of inhibin B in individuals with severe damage to the testis as a result of germ cell depletion. Inhibin B has proved valuable in epidemiological studies exploring male infertility with data showing that inhibin B combined with FSH measurements has a higher positive predictive value for detecting male infertility than either alone. Inhibin B is proposed as a potential biomarker of testicular toxicity in rodent toxicity studies to compliment traditional endpoints. In pharmaceutical development, inhibin B might allow better linkage between animal study results and subsequent monitoring of testicular function in clinical trials. An international, intercompany project has been initiated to evaluate the overall suitability and limitations of inhibin B as a biomarker of testicular toxicity.</abstract><cop>Netherlands</cop><pmid>17192034</pmid><doi>10.3233/CBM-2005-1109</doi><tpages>17</tpages></addata></record> |
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subjects | Adult Animals Biomarkers - analysis Drug-Related Side Effects and Adverse Reactions - diagnosis Humans Inhibins - analysis Inhibins - biosynthesis Inhibins - chemistry Inhibins - physiology Male Models, Biological Rodentia Spermatogenesis - physiology Testicular Diseases - chemically induced Testis - drug effects Testis - growth & development Testis - metabolism |
title | Inhibin B as a potential biomarker of testicular toxicity |
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