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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer biomarkers : section A of Disease markers 2005, Vol.1 (1), p.75-91
Hauptverfasser: Stewart, Jane, Turner, Katie J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 91
container_issue 1
container_start_page 75
container_title Cancer biomarkers : section A of Disease markers
container_volume 1
creator Stewart, Jane
Turner, Katie J
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.
doi_str_mv 10.3233/CBM-2005-1109
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_745633724</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>745633724</sourcerecordid><originalsourceid>FETCH-LOGICAL-c238t-b46db94b7fb03cb1c85a029192ffcf1125f6b65617b8ad48eed268cd8c391d693</originalsourceid><addsrcrecordid>eNpFkDtPwzAURi0EoqUwsiJvTAa_Y4-04lGpiAVmy3ZsYUiTEicS_fc4aiWme4ej77v3AHBN8B2jjN2vlq-IYiwQIVifgDlRlUBKaHpadlFxhIlgM3CR8xfGnBGqz8GMVERTzPgc6HX7mVxq4RLaDC3cdUNoh2Qb6FK3tf136GEX4RDykPzY2B4O3W_yadhfgrNomxyujnMBPp4e31cvaPP2vF49bJCnTA3IcVk7zV0VHWbeEa-ExVSX_hh9JISKKJ0UklRO2ZqrEGoqla-VZ5rUUrMFuD3k7vruZyx3mG3KPjSNbUM3ZlNxIRmrKC8kOpC-73LuQzS7PpUf9oZgM8kyRZaZZJlJVuFvjsmj24b6nz7aYX_LHGPI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>745633724</pqid></control><display><type>article</type><title>Inhibin B as a potential biomarker of testicular toxicity</title><source>MEDLINE</source><source>Sage Journals GOLD Open Access 2024</source><creator>Stewart, Jane ; Turner, Katie J</creator><contributor>Dixit, Rakesh</contributor><creatorcontrib>Stewart, Jane ; Turner, Katie J ; Dixit, Rakesh</creatorcontrib><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><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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 1574-0153
ispartof Cancer biomarkers : section A of Disease markers, 2005, Vol.1 (1), p.75-91
issn 1574-0153
1875-8592
language eng
recordid cdi_proquest_miscellaneous_745633724
source MEDLINE; Sage Journals GOLD Open Access 2024
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T06%3A52%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inhibin%20B%20as%20a%20potential%20biomarker%20of%20testicular%20toxicity&rft.jtitle=Cancer%20biomarkers%20:%20section%20A%20of%20Disease%20markers&rft.au=Stewart,%20Jane&rft.date=2005&rft.volume=1&rft.issue=1&rft.spage=75&rft.epage=91&rft.pages=75-91&rft.issn=1574-0153&rft.eissn=1875-8592&rft_id=info:doi/10.3233/CBM-2005-1109&rft_dat=%3Cproquest_cross%3E745633724%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=745633724&rft_id=info:pmid/17192034&rfr_iscdi=true