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Complement C4-A and Plasminogen as Potential Biomarkers for Prediction of Papillary Thyroid Carcinoma
Early diagnosis and therapy of papillary thyroid carcinoma (PTC) is essential for reducing recurrence and improving the long-term survival. In this study, we aimed to investigate the proteome profile of plasma and screen unique proteins which could be used as a biomarker for predicting PTC. Serum sa...
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Published in: | Frontiers in endocrinology (Lausanne) 2021-11, Vol.12, p.737638-737638 |
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creator | Wang, Yichao Zhou, Shengliang Wang, Dun Wei, Tao Zhu, Jingqiang Li, Zhihui |
description | Early diagnosis and therapy of papillary thyroid carcinoma (PTC) is essential for reducing recurrence and improving the long-term survival. In this study, we aimed to investigate the proteome profile of plasma and screen unique proteins which could be used as a biomarker for predicting PTC.
Serum samples were collected from 29 PTC patients and 29 nodular goiter (NG) patients. Five PTC serum samples and five NG serum samples were selected for proteome profiles by proteomics. Eight proteins in PTC and NG serum samples were selected for confirmation by enzyme-linked immunosorbent assay analysis. Receiver operating characteristic curves was used to evaluate the diagnostic value of potential biomarkers.
Complement C4-A (C4A) and plasminogen (PLG) were significantly lower in serum samples of PTC patients compared with NG patients. C4A was observed to have excellent diagnostic accuracy for PTC, with a sensitivity of 91.67% and specificity of 83.33%. The diagnostic value of PLG for PTC was demonstrated by a sensitivity at 87.50% and specificity at 75.00%. The AUC for C4A and PLG was 0.97 ± 0.02 and 0.89 ± 0.05.
C4A and PLG appeared to be excellent potential biomarkers for the prediction of PTC. |
doi_str_mv | 10.3389/fendo.2021.737638 |
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Serum samples were collected from 29 PTC patients and 29 nodular goiter (NG) patients. Five PTC serum samples and five NG serum samples were selected for proteome profiles by proteomics. Eight proteins in PTC and NG serum samples were selected for confirmation by enzyme-linked immunosorbent assay analysis. Receiver operating characteristic curves was used to evaluate the diagnostic value of potential biomarkers.
Complement C4-A (C4A) and plasminogen (PLG) were significantly lower in serum samples of PTC patients compared with NG patients. C4A was observed to have excellent diagnostic accuracy for PTC, with a sensitivity of 91.67% and specificity of 83.33%. The diagnostic value of PLG for PTC was demonstrated by a sensitivity at 87.50% and specificity at 75.00%. The AUC for C4A and PLG was 0.97 ± 0.02 and 0.89 ± 0.05.
C4A and PLG appeared to be excellent potential biomarkers for the prediction of PTC.</description><identifier>ISSN: 1664-2392</identifier><identifier>EISSN: 1664-2392</identifier><identifier>DOI: 10.3389/fendo.2021.737638</identifier><identifier>PMID: 34803909</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>Adult ; biomarker ; Biomarkers, Tumor - blood ; complement C4-A ; Complement C4a - metabolism ; Endocrinology ; Female ; Humans ; Male ; Middle Aged ; papillary thyroid carcinoma ; plasminogen ; Plasminogen - metabolism ; prediction ; Proteomics ; Sensitivity and Specificity ; Thyroid Cancer, Papillary - blood ; Thyroid Cancer, Papillary - diagnosis ; Thyroid Cancer, Papillary - pathology ; Thyroid Neoplasms - blood ; Thyroid Neoplasms - diagnosis ; Thyroid Neoplasms - pathology</subject><ispartof>Frontiers in endocrinology (Lausanne), 2021-11, Vol.12, p.737638-737638</ispartof><rights>Copyright © 2021 Wang, Zhou, Wang, Wei, Zhu and Li.</rights><rights>Copyright © 2021 Wang, Zhou, Wang, Wei, Zhu and Li 2021 Wang, Zhou, Wang, Wei, Zhu and Li</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-452a555aa053e66beac919131db6773da9d748fe5ff26ce001a9a2835c4a31663</citedby><cites>FETCH-LOGICAL-c465t-452a555aa053e66beac919131db6773da9d748fe5ff26ce001a9a2835c4a31663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603925/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603925/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34803909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yichao</creatorcontrib><creatorcontrib>Zhou, Shengliang</creatorcontrib><creatorcontrib>Wang, Dun</creatorcontrib><creatorcontrib>Wei, Tao</creatorcontrib><creatorcontrib>Zhu, Jingqiang</creatorcontrib><creatorcontrib>Li, Zhihui</creatorcontrib><title>Complement C4-A and Plasminogen as Potential Biomarkers for Prediction of Papillary Thyroid Carcinoma</title><title>Frontiers in endocrinology (Lausanne)</title><addtitle>Front Endocrinol (Lausanne)</addtitle><description>Early diagnosis and therapy of papillary thyroid carcinoma (PTC) is essential for reducing recurrence and improving the long-term survival. In this study, we aimed to investigate the proteome profile of plasma and screen unique proteins which could be used as a biomarker for predicting PTC.
Serum samples were collected from 29 PTC patients and 29 nodular goiter (NG) patients. Five PTC serum samples and five NG serum samples were selected for proteome profiles by proteomics. Eight proteins in PTC and NG serum samples were selected for confirmation by enzyme-linked immunosorbent assay analysis. Receiver operating characteristic curves was used to evaluate the diagnostic value of potential biomarkers.
Complement C4-A (C4A) and plasminogen (PLG) were significantly lower in serum samples of PTC patients compared with NG patients. C4A was observed to have excellent diagnostic accuracy for PTC, with a sensitivity of 91.67% and specificity of 83.33%. The diagnostic value of PLG for PTC was demonstrated by a sensitivity at 87.50% and specificity at 75.00%. The AUC for C4A and PLG was 0.97 ± 0.02 and 0.89 ± 0.05.
C4A and PLG appeared to be excellent potential biomarkers for the prediction of PTC.</description><subject>Adult</subject><subject>biomarker</subject><subject>Biomarkers, Tumor - blood</subject><subject>complement C4-A</subject><subject>Complement C4a - metabolism</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>papillary thyroid carcinoma</subject><subject>plasminogen</subject><subject>Plasminogen - metabolism</subject><subject>prediction</subject><subject>Proteomics</subject><subject>Sensitivity and Specificity</subject><subject>Thyroid Cancer, Papillary - blood</subject><subject>Thyroid Cancer, Papillary - diagnosis</subject><subject>Thyroid Cancer, Papillary - pathology</subject><subject>Thyroid Neoplasms - blood</subject><subject>Thyroid Neoplasms - diagnosis</subject><subject>Thyroid Neoplasms - pathology</subject><issn>1664-2392</issn><issn>1664-2392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkU1P3DAQhi3UChDlB3BBPvaSxd-xL5Vo1A8kpO6Bnq2J7SymSby1s5X239ewgMCXsTwzj2feF6ELSlaca3M1hNmnFSOMrlreKq6P0ClVSjSMG_bhzf0EnZfyQOoRhBqjj9EJF5pwQ8wpCl2atmOYwrzgTjTXGGaP1yOUKc5pE2YMBa_TUtMRRvw1pgnyn5ALHlLG6xx8dEtMM04DXsM2jiPkPb673-cUPe4gu4qZ4BP6OMBYwvlzPEO_v3-76342t79-3HTXt40TSi6NkAyklABE8qBUH8AZaiinvldtyz0Y3wo9BDkMTLlACAUDTHPpBPC6Lz9DNweuT_BgtznWafc2QbRPDylvLOQlujFYz_ueQ08VbZWQvQbqWE9dC9xwL6WurC8H1nbXT8G7KkGG8R30fWaO93aT_lmtqrZMVsDnZ0BOf3ehLHaKxYUq0RzSrlimCNGMUCpqKT2UupxKyWF4_YYS--i2fXLbPrptD27Xnsu38712vHjL_wPm_qdR</recordid><startdate>20211105</startdate><enddate>20211105</enddate><creator>Wang, Yichao</creator><creator>Zhou, Shengliang</creator><creator>Wang, Dun</creator><creator>Wei, Tao</creator><creator>Zhu, Jingqiang</creator><creator>Li, Zhihui</creator><general>Frontiers Media S.A</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><scope>DOA</scope></search><sort><creationdate>20211105</creationdate><title>Complement C4-A and Plasminogen as Potential Biomarkers for Prediction of Papillary Thyroid Carcinoma</title><author>Wang, Yichao ; Zhou, Shengliang ; Wang, Dun ; Wei, Tao ; Zhu, Jingqiang ; Li, Zhihui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-452a555aa053e66beac919131db6773da9d748fe5ff26ce001a9a2835c4a31663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>biomarker</topic><topic>Biomarkers, Tumor - blood</topic><topic>complement C4-A</topic><topic>Complement C4a - metabolism</topic><topic>Endocrinology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>papillary thyroid carcinoma</topic><topic>plasminogen</topic><topic>Plasminogen - metabolism</topic><topic>prediction</topic><topic>Proteomics</topic><topic>Sensitivity and Specificity</topic><topic>Thyroid Cancer, Papillary - blood</topic><topic>Thyroid Cancer, Papillary - diagnosis</topic><topic>Thyroid Cancer, Papillary - pathology</topic><topic>Thyroid Neoplasms - blood</topic><topic>Thyroid Neoplasms - diagnosis</topic><topic>Thyroid Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yichao</creatorcontrib><creatorcontrib>Zhou, Shengliang</creatorcontrib><creatorcontrib>Wang, Dun</creatorcontrib><creatorcontrib>Wei, Tao</creatorcontrib><creatorcontrib>Zhu, Jingqiang</creatorcontrib><creatorcontrib>Li, Zhihui</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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in endocrinology (Lausanne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yichao</au><au>Zhou, Shengliang</au><au>Wang, Dun</au><au>Wei, Tao</au><au>Zhu, Jingqiang</au><au>Li, Zhihui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complement C4-A and Plasminogen as Potential Biomarkers for Prediction of Papillary Thyroid Carcinoma</atitle><jtitle>Frontiers in endocrinology (Lausanne)</jtitle><addtitle>Front Endocrinol (Lausanne)</addtitle><date>2021-11-05</date><risdate>2021</risdate><volume>12</volume><spage>737638</spage><epage>737638</epage><pages>737638-737638</pages><issn>1664-2392</issn><eissn>1664-2392</eissn><abstract>Early diagnosis and therapy of papillary thyroid carcinoma (PTC) is essential for reducing recurrence and improving the long-term survival. In this study, we aimed to investigate the proteome profile of plasma and screen unique proteins which could be used as a biomarker for predicting PTC.
Serum samples were collected from 29 PTC patients and 29 nodular goiter (NG) patients. Five PTC serum samples and five NG serum samples were selected for proteome profiles by proteomics. Eight proteins in PTC and NG serum samples were selected for confirmation by enzyme-linked immunosorbent assay analysis. Receiver operating characteristic curves was used to evaluate the diagnostic value of potential biomarkers.
Complement C4-A (C4A) and plasminogen (PLG) were significantly lower in serum samples of PTC patients compared with NG patients. C4A was observed to have excellent diagnostic accuracy for PTC, with a sensitivity of 91.67% and specificity of 83.33%. The diagnostic value of PLG for PTC was demonstrated by a sensitivity at 87.50% and specificity at 75.00%. The AUC for C4A and PLG was 0.97 ± 0.02 and 0.89 ± 0.05.
C4A and PLG appeared to be excellent potential biomarkers for the prediction of PTC.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>34803909</pmid><doi>10.3389/fendo.2021.737638</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult biomarker Biomarkers, Tumor - blood complement C4-A Complement C4a - metabolism Endocrinology Female Humans Male Middle Aged papillary thyroid carcinoma plasminogen Plasminogen - metabolism prediction Proteomics Sensitivity and Specificity Thyroid Cancer, Papillary - blood Thyroid Cancer, Papillary - diagnosis Thyroid Cancer, Papillary - pathology Thyroid Neoplasms - blood Thyroid Neoplasms - diagnosis Thyroid Neoplasms - pathology |
title | Complement C4-A and Plasminogen as Potential Biomarkers for Prediction of Papillary Thyroid Carcinoma |
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