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Inhibin forms in serum from postmenopausal women with ovarian cancers

BACKGROUND AND OBJECTIVE Previous studies have shown that serum inhibin as measured by α subunit‐directed radioimmunoassay (RIA) and inhibin A ELISA was elevated in postmenopausal women with mucinous and granulosa cell cancers, with the RIA showing a more frequent elevation than the inhibin A ELISA....

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Published in:Clinical endocrinology (Oxford) 1999-03, Vol.50 (3), p.381-386
Main Authors: Robertson, David M., Cahir, Nicholas, Burger, Henry G., Mamers, Pamela, Groome, Nigel
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description BACKGROUND AND OBJECTIVE Previous studies have shown that serum inhibin as measured by α subunit‐directed radioimmunoassay (RIA) and inhibin A ELISA was elevated in postmenopausal women with mucinous and granulosa cell cancers, with the RIA showing a more frequent elevation than the inhibin A ELISA. It was thus hypothesised that these cancers may also produce inhibin B or the free α subunit. The aim of the study was to identify the forms of inhibin found in a range of ovarian cancers using a range of inhibin assays with varying specificities. DESIGN Serum samples obtained from women with ovarian cancer were assayed by inhibin B ELISA and Pro‐αC subunit ELISA and compared with inhibin RIA and inhibin A ELISA. PATIENTS Blood samples were obtained from 34 postmenopausal women (>55 years) with no history of endocrine disease and from women with ovarian serous cystadenocarcinomas (n = 66), mucinous cystadenocarcinomas (n = 20), granulosa cell tumours (n = 9 − 11), miscellaneous ovarian cancers (n = 46) and non ovarian cancers (n = 23). MEASUREMENTS Inhibin B and inhibin Pro‐αC subunit levels were determined by ELISA and compared to values obtained by RIA and inhibin A ELISA. Cancers were discriminated from controls based on values obtained 2SD above the geometric mean of the control values. RESULTS Granulosa cell tumours were detected by RIA and inhibin B ELISA (100%), Pro‐αC ELISA (90%) and inhibin A ELISA (77%). Mucinous tumours were detected by RIA (70%), inhibin B ELISA (60%), Pro‐αC ELISA (55%) and inhibin A (20%). Serous tumours were detected by RIA (35%) and the other assays (
doi_str_mv 10.1046/j.1365-2265.1999.00656.x
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It was thus hypothesised that these cancers may also produce inhibin B or the free α subunit. The aim of the study was to identify the forms of inhibin found in a range of ovarian cancers using a range of inhibin assays with varying specificities. DESIGN Serum samples obtained from women with ovarian cancer were assayed by inhibin B ELISA and Pro‐αC subunit ELISA and compared with inhibin RIA and inhibin A ELISA. PATIENTS Blood samples were obtained from 34 postmenopausal women (&gt;55 years) with no history of endocrine disease and from women with ovarian serous cystadenocarcinomas (n = 66), mucinous cystadenocarcinomas (n = 20), granulosa cell tumours (n = 9 − 11), miscellaneous ovarian cancers (n = 46) and non ovarian cancers (n = 23). MEASUREMENTS Inhibin B and inhibin Pro‐αC subunit levels were determined by ELISA and compared to values obtained by RIA and inhibin A ELISA. Cancers were discriminated from controls based on values obtained 2SD above the geometric mean of the control values. RESULTS Granulosa cell tumours were detected by RIA and inhibin B ELISA (100%), Pro‐αC ELISA (90%) and inhibin A ELISA (77%). Mucinous tumours were detected by RIA (70%), inhibin B ELISA (60%), Pro‐αC ELISA (55%) and inhibin A (20%). Serous tumours were detected by RIA (35%) and the other assays (&lt;15%). Miscellaneous tumours were detected by RIA (41%) and other assays &lt;30%. CONCLUSIONS Ovarian neoplasms may produce a variety of peptides related to the inhibins, including dimeric inhibin A and B. Inhibin B is detected in more ovarian cancers than inhibin A but does not discriminate as well as the α subunit directed assays. The higher discrimination index obtained with the RIA compared to the Pro‐αC ELISA suggests that assays detecting all inhibin forms containing the α subunit and not just those detecting the Pro‐αC subunit will provide the most useful detection method.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1046/j.1365-2265.1999.00656.x</identifier><identifier>PMID: 10435065</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford BSL: Blackwell Science Ltd</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Enzyme-Linked Immunosorbent Assay - methods ; Female ; Female genital diseases ; Follicle Stimulating Hormone - blood ; Granulosa Cell Tumor - blood ; Granulosa Cell Tumor - diagnosis ; Gynecology. Andrology. Obstetrics ; Humans ; Inhibins - blood ; Medical sciences ; Middle Aged ; Neoplasms, Cystic, Mucinous, and Serous - blood ; Neoplasms, Cystic, Mucinous, and Serous - diagnosis ; Ovarian Neoplasms - blood ; Ovarian Neoplasms - diagnosis ; Peptides - blood ; Postmenopause - blood ; Predictive Value of Tests ; Prostatic Secretory Proteins ; Radioimmunoassay ; Tumors</subject><ispartof>Clinical endocrinology (Oxford), 1999-03, Vol.50 (3), p.381-386</ispartof><rights>Blackwell Science Ltd, Oxford</rights><rights>1999 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Mar 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4586-c040103469e6156a6cc86b27e0533baf99313cc999821d1ac4a49a6dddcdcf1b3</citedby><cites>FETCH-LOGICAL-c4586-c040103469e6156a6cc86b27e0533baf99313cc999821d1ac4a49a6dddcdcf1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1736351$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10435065$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Robertson, David M.</creatorcontrib><creatorcontrib>Cahir, Nicholas</creatorcontrib><creatorcontrib>Burger, Henry G.</creatorcontrib><creatorcontrib>Mamers, Pamela</creatorcontrib><creatorcontrib>Groome, Nigel</creatorcontrib><title>Inhibin forms in serum from postmenopausal women with ovarian cancers</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clinical Endocrinology</addtitle><description>BACKGROUND AND OBJECTIVE Previous studies have shown that serum inhibin as measured by α subunit‐directed radioimmunoassay (RIA) and inhibin A ELISA was elevated in postmenopausal women with mucinous and granulosa cell cancers, with the RIA showing a more frequent elevation than the inhibin A ELISA. It was thus hypothesised that these cancers may also produce inhibin B or the free α subunit. The aim of the study was to identify the forms of inhibin found in a range of ovarian cancers using a range of inhibin assays with varying specificities. DESIGN Serum samples obtained from women with ovarian cancer were assayed by inhibin B ELISA and Pro‐αC subunit ELISA and compared with inhibin RIA and inhibin A ELISA. PATIENTS Blood samples were obtained from 34 postmenopausal women (&gt;55 years) with no history of endocrine disease and from women with ovarian serous cystadenocarcinomas (n = 66), mucinous cystadenocarcinomas (n = 20), granulosa cell tumours (n = 9 − 11), miscellaneous ovarian cancers (n = 46) and non ovarian cancers (n = 23). MEASUREMENTS Inhibin B and inhibin Pro‐αC subunit levels were determined by ELISA and compared to values obtained by RIA and inhibin A ELISA. Cancers were discriminated from controls based on values obtained 2SD above the geometric mean of the control values. RESULTS Granulosa cell tumours were detected by RIA and inhibin B ELISA (100%), Pro‐αC ELISA (90%) and inhibin A ELISA (77%). Mucinous tumours were detected by RIA (70%), inhibin B ELISA (60%), Pro‐αC ELISA (55%) and inhibin A (20%). Serous tumours were detected by RIA (35%) and the other assays (&lt;15%). Miscellaneous tumours were detected by RIA (41%) and other assays &lt;30%. CONCLUSIONS Ovarian neoplasms may produce a variety of peptides related to the inhibins, including dimeric inhibin A and B. Inhibin B is detected in more ovarian cancers than inhibin A but does not discriminate as well as the α subunit directed assays. 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Andrology. Obstetrics</topic><topic>Humans</topic><topic>Inhibins - blood</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasms, Cystic, Mucinous, and Serous - blood</topic><topic>Neoplasms, Cystic, Mucinous, and Serous - diagnosis</topic><topic>Ovarian Neoplasms - blood</topic><topic>Ovarian Neoplasms - diagnosis</topic><topic>Peptides - blood</topic><topic>Postmenopause - blood</topic><topic>Predictive Value of Tests</topic><topic>Prostatic Secretory Proteins</topic><topic>Radioimmunoassay</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robertson, David M.</creatorcontrib><creatorcontrib>Cahir, Nicholas</creatorcontrib><creatorcontrib>Burger, Henry G.</creatorcontrib><creatorcontrib>Mamers, Pamela</creatorcontrib><creatorcontrib>Groome, Nigel</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robertson, David M.</au><au>Cahir, Nicholas</au><au>Burger, Henry G.</au><au>Mamers, Pamela</au><au>Groome, Nigel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibin forms in serum from postmenopausal women with ovarian cancers</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clinical Endocrinology</addtitle><date>1999-03</date><risdate>1999</risdate><volume>50</volume><issue>3</issue><spage>381</spage><epage>386</epage><pages>381-386</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>BACKGROUND AND OBJECTIVE Previous studies have shown that serum inhibin as measured by α subunit‐directed radioimmunoassay (RIA) and inhibin A ELISA was elevated in postmenopausal women with mucinous and granulosa cell cancers, with the RIA showing a more frequent elevation than the inhibin A ELISA. It was thus hypothesised that these cancers may also produce inhibin B or the free α subunit. The aim of the study was to identify the forms of inhibin found in a range of ovarian cancers using a range of inhibin assays with varying specificities. DESIGN Serum samples obtained from women with ovarian cancer were assayed by inhibin B ELISA and Pro‐αC subunit ELISA and compared with inhibin RIA and inhibin A ELISA. PATIENTS Blood samples were obtained from 34 postmenopausal women (&gt;55 years) with no history of endocrine disease and from women with ovarian serous cystadenocarcinomas (n = 66), mucinous cystadenocarcinomas (n = 20), granulosa cell tumours (n = 9 − 11), miscellaneous ovarian cancers (n = 46) and non ovarian cancers (n = 23). MEASUREMENTS Inhibin B and inhibin Pro‐αC subunit levels were determined by ELISA and compared to values obtained by RIA and inhibin A ELISA. Cancers were discriminated from controls based on values obtained 2SD above the geometric mean of the control values. RESULTS Granulosa cell tumours were detected by RIA and inhibin B ELISA (100%), Pro‐αC ELISA (90%) and inhibin A ELISA (77%). Mucinous tumours were detected by RIA (70%), inhibin B ELISA (60%), Pro‐αC ELISA (55%) and inhibin A (20%). Serous tumours were detected by RIA (35%) and the other assays (&lt;15%). Miscellaneous tumours were detected by RIA (41%) and other assays &lt;30%. CONCLUSIONS Ovarian neoplasms may produce a variety of peptides related to the inhibins, including dimeric inhibin A and B. Inhibin B is detected in more ovarian cancers than inhibin A but does not discriminate as well as the α subunit directed assays. The higher discrimination index obtained with the RIA compared to the Pro‐αC ELISA suggests that assays detecting all inhibin forms containing the α subunit and not just those detecting the Pro‐αC subunit will provide the most useful detection method.</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd</pub><pmid>10435065</pmid><doi>10.1046/j.1365-2265.1999.00656.x</doi><tpages>6</tpages></addata></record>
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subjects Aged
Aged, 80 and over
Biological and medical sciences
Enzyme-Linked Immunosorbent Assay - methods
Female
Female genital diseases
Follicle Stimulating Hormone - blood
Granulosa Cell Tumor - blood
Granulosa Cell Tumor - diagnosis
Gynecology. Andrology. Obstetrics
Humans
Inhibins - blood
Medical sciences
Middle Aged
Neoplasms, Cystic, Mucinous, and Serous - blood
Neoplasms, Cystic, Mucinous, and Serous - diagnosis
Ovarian Neoplasms - blood
Ovarian Neoplasms - diagnosis
Peptides - blood
Postmenopause - blood
Predictive Value of Tests
Prostatic Secretory Proteins
Radioimmunoassay
Tumors
title Inhibin forms in serum from postmenopausal women with ovarian cancers
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