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TROP-2 expression in papillary thyroid carcinoma: Potential Diagnostic Utility
TROP-2 is a type I transmembrane glycoprotein which is over-expressed in various malignancies, and is related to epithelial cell adhesion molecule (EpCAM), also called TROP-1, gp40, and KSA. In this study, we evaluated TROP-2 expression in papillary thyroid carcinoma (PTC) and compared it to other t...
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Published in: | Diagnostic cytopathology 2016-01, Vol.44 (1), p.26-31 |
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description | TROP-2 is a type I transmembrane glycoprotein which is over-expressed in various malignancies, and is related to epithelial cell adhesion molecule (EpCAM), also called TROP-1, gp40, and KSA. In this study, we evaluated TROP-2 expression in papillary thyroid carcinoma (PTC) and compared it to other thyroid neoplastic and non-neoplastic lesions. Immunohistochemical (IHC) evaluation for TROP-2 was performed on 137 thyroid fine needle aspiration (FNA) cell blocks (CB) which included classic PTC (64), follicular variant PTC (FVPTC) (10), anaplastic thyroid carcinoma (AC) (2), medullary carcinoma (MC) (8), follicular neoplasms (FN) (8), Hurthle cell neoplasms (HCN) (9), follicular lesion of uncertain significance (FLUS) (12), and benign thyroid nodule (BTN) (24). IHC for TROP-2 expression was also performed on 331 BTN and malignant tumor tissue sections in tissue microarray (TMA). Membranous staining in >5% of tumor cells was considered positive. TROP-2 stained 61 of 64 PTC CB, 7 of 10 FVPTC CB, and 9 of 12 FLUS CB. All other cases were negative for TROP-2. TROP-2 showed a sensitivity of 95.31% and specificity of 89% for classic PTC in FNA CB. In TMA samples, TROP-2 stained 54 of 60 classic PTC cases and hence showed a high sensitivity and specificity. All BTN in CB and TMA were negative. We conclude that TROP-2 is a highly sensitive and specific IHC marker for identifying classic PTC. TROP-2 may play an important role in diagnosing classic PTC, especially in equivocal cases. This study also identifies a strong role for TROP-2 in separating PTC from BTN. |
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In this study, we evaluated TROP-2 expression in papillary thyroid carcinoma (PTC) and compared it to other thyroid neoplastic and non-neoplastic lesions. Immunohistochemical (IHC) evaluation for TROP-2 was performed on 137 thyroid fine needle aspiration (FNA) cell blocks (CB) which included classic PTC (64), follicular variant PTC (FVPTC) (10), anaplastic thyroid carcinoma (AC) (2), medullary carcinoma (MC) (8), follicular neoplasms (FN) (8), Hurthle cell neoplasms (HCN) (9), follicular lesion of uncertain significance (FLUS) (12), and benign thyroid nodule (BTN) (24). IHC for TROP-2 expression was also performed on 331 BTN and malignant tumor tissue sections in tissue microarray (TMA). Membranous staining in >5% of tumor cells was considered positive. TROP-2 stained 61 of 64 PTC CB, 7 of 10 FVPTC CB, and 9 of 12 FLUS CB. All other cases were negative for TROP-2. TROP-2 showed a sensitivity of 95.31% and specificity of 89% for classic PTC in FNA CB. In TMA samples, TROP-2 stained 54 of 60 classic PTC cases and hence showed a high sensitivity and specificity. All BTN in CB and TMA were negative. We conclude that TROP-2 is a highly sensitive and specific IHC marker for identifying classic PTC. TROP-2 may play an important role in diagnosing classic PTC, especially in equivocal cases. This study also identifies a strong role for TROP-2 in separating PTC from BTN.</description><identifier>ISSN: 8755-1039</identifier><identifier>EISSN: 1097-0339</identifier><identifier>DOI: 10.1002/dc.23382</identifier><identifier>PMID: 26481593</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma, Follicular - diagnosis ; Adenocarcinoma, Follicular - genetics ; Adenocarcinoma, Follicular - pathology ; Antigens, Neoplasm - genetics ; Biomarkers, Tumor - genetics ; Biopsy, Fine-Needle ; Carcinoma - diagnosis ; Carcinoma - genetics ; Carcinoma - pathology ; Carcinoma, Medullary - diagnosis ; Carcinoma, Medullary - genetics ; Carcinoma, Medullary - pathology ; Carcinoma, Neuroendocrine - diagnosis ; Carcinoma, Neuroendocrine - genetics ; Carcinoma, Neuroendocrine - pathology ; Carcinoma, Papillary ; Cell Adhesion Molecules - genetics ; Diagnosis, Differential ; Gene Expression ; Humans ; Immunohistochemistry ; Retrospective Studies ; Sensitivity and Specificity ; Thyroid Carcinoma, Anaplastic - diagnosis ; Thyroid Carcinoma, Anaplastic - genetics ; Thyroid Carcinoma, Anaplastic - pathology ; Thyroid Neoplasms - diagnosis ; Thyroid Neoplasms - genetics ; Thyroid Neoplasms - pathology ; Thyroid Nodule - diagnosis ; Thyroid Nodule - genetics ; Thyroid Nodule - pathology ; Tissue Array Analysis</subject><ispartof>Diagnostic cytopathology, 2016-01, Vol.44 (1), p.26-31</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c244t-b53c5b90bba333607794997185e3f22c024993c5036b9db3a8ec5313b6efe76f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26481593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Simms, Anthony</creatorcontrib><creatorcontrib>Jacob, Reuben P</creatorcontrib><creatorcontrib>Cohen, Cynthia</creatorcontrib><creatorcontrib>Siddiqui, Momin T</creatorcontrib><title>TROP-2 expression in papillary thyroid carcinoma: Potential Diagnostic Utility</title><title>Diagnostic cytopathology</title><addtitle>Diagn Cytopathol</addtitle><description>TROP-2 is a type I transmembrane glycoprotein which is over-expressed in various malignancies, and is related to epithelial cell adhesion molecule (EpCAM), also called TROP-1, gp40, and KSA. In this study, we evaluated TROP-2 expression in papillary thyroid carcinoma (PTC) and compared it to other thyroid neoplastic and non-neoplastic lesions. Immunohistochemical (IHC) evaluation for TROP-2 was performed on 137 thyroid fine needle aspiration (FNA) cell blocks (CB) which included classic PTC (64), follicular variant PTC (FVPTC) (10), anaplastic thyroid carcinoma (AC) (2), medullary carcinoma (MC) (8), follicular neoplasms (FN) (8), Hurthle cell neoplasms (HCN) (9), follicular lesion of uncertain significance (FLUS) (12), and benign thyroid nodule (BTN) (24). IHC for TROP-2 expression was also performed on 331 BTN and malignant tumor tissue sections in tissue microarray (TMA). Membranous staining in >5% of tumor cells was considered positive. TROP-2 stained 61 of 64 PTC CB, 7 of 10 FVPTC CB, and 9 of 12 FLUS CB. All other cases were negative for TROP-2. TROP-2 showed a sensitivity of 95.31% and specificity of 89% for classic PTC in FNA CB. In TMA samples, TROP-2 stained 54 of 60 classic PTC cases and hence showed a high sensitivity and specificity. All BTN in CB and TMA were negative. We conclude that TROP-2 is a highly sensitive and specific IHC marker for identifying classic PTC. TROP-2 may play an important role in diagnosing classic PTC, especially in equivocal cases. This study also identifies a strong role for TROP-2 in separating PTC from BTN.</description><subject>Adenocarcinoma, Follicular - diagnosis</subject><subject>Adenocarcinoma, Follicular - genetics</subject><subject>Adenocarcinoma, Follicular - pathology</subject><subject>Antigens, Neoplasm - genetics</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biopsy, Fine-Needle</subject><subject>Carcinoma - diagnosis</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma, Medullary - diagnosis</subject><subject>Carcinoma, Medullary - genetics</subject><subject>Carcinoma, Medullary - pathology</subject><subject>Carcinoma, Neuroendocrine - diagnosis</subject><subject>Carcinoma, Neuroendocrine - genetics</subject><subject>Carcinoma, Neuroendocrine - pathology</subject><subject>Carcinoma, Papillary</subject><subject>Cell Adhesion Molecules - genetics</subject><subject>Diagnosis, Differential</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Retrospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Thyroid Carcinoma, Anaplastic - diagnosis</subject><subject>Thyroid Carcinoma, Anaplastic - genetics</subject><subject>Thyroid Carcinoma, Anaplastic - pathology</subject><subject>Thyroid Neoplasms - diagnosis</subject><subject>Thyroid Neoplasms - genetics</subject><subject>Thyroid Neoplasms - pathology</subject><subject>Thyroid Nodule - diagnosis</subject><subject>Thyroid Nodule - genetics</subject><subject>Thyroid Nodule - pathology</subject><subject>Tissue Array Analysis</subject><issn>8755-1039</issn><issn>1097-0339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpFkF1LwzAUhoMobk7BXyC59KYzyWnaxjvZ_ILhhmzXJUlTjbRNTTJw_96qU68OBx5e3vdB6JySKSWEXVV6ygAKdoDGlIg8IQDiEI2LnPOEEhAjdBLCGyFEMJodoxHL0oJyAWP0tH5erhKGzUfvTQjWddh2uJe9bRrpdzi-7ryzFdbSa9u5Vl7jlYumi1Y2eG7lS-dCtBpvom1s3J2io1o2wZzt7wRt7m7Xs4dksbx_nN0sEs3SNCaKg-ZKEKUkAGQkz0UqRE4LbqBmTBM2vANCIFOiUiALozlQUJmpTZ7VMEGXP7m9d-9bE2LZ2qDN0LkzbhtKmqciGxYW9B_V3oXgTV323rbDtpKS8steWeny296AXuxTt6o11R_4qws-AYDHaTM</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Simms, Anthony</creator><creator>Jacob, Reuben P</creator><creator>Cohen, Cynthia</creator><creator>Siddiqui, Momin T</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>7X8</scope></search><sort><creationdate>201601</creationdate><title>TROP-2 expression in papillary thyroid carcinoma: Potential Diagnostic Utility</title><author>Simms, Anthony ; Jacob, Reuben P ; Cohen, Cynthia ; Siddiqui, Momin T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c244t-b53c5b90bba333607794997185e3f22c024993c5036b9db3a8ec5313b6efe76f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenocarcinoma, Follicular - diagnosis</topic><topic>Adenocarcinoma, Follicular - genetics</topic><topic>Adenocarcinoma, Follicular - pathology</topic><topic>Antigens, Neoplasm - genetics</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biopsy, Fine-Needle</topic><topic>Carcinoma - diagnosis</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma, Medullary - diagnosis</topic><topic>Carcinoma, Medullary - genetics</topic><topic>Carcinoma, Medullary - pathology</topic><topic>Carcinoma, Neuroendocrine - diagnosis</topic><topic>Carcinoma, Neuroendocrine - genetics</topic><topic>Carcinoma, Neuroendocrine - pathology</topic><topic>Carcinoma, Papillary</topic><topic>Cell Adhesion Molecules - genetics</topic><topic>Diagnosis, Differential</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Retrospective Studies</topic><topic>Sensitivity and Specificity</topic><topic>Thyroid Carcinoma, Anaplastic - diagnosis</topic><topic>Thyroid Carcinoma, Anaplastic - genetics</topic><topic>Thyroid Carcinoma, Anaplastic - pathology</topic><topic>Thyroid Neoplasms - diagnosis</topic><topic>Thyroid Neoplasms - genetics</topic><topic>Thyroid Neoplasms - pathology</topic><topic>Thyroid Nodule - diagnosis</topic><topic>Thyroid Nodule - genetics</topic><topic>Thyroid Nodule - pathology</topic><topic>Tissue Array Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simms, Anthony</creatorcontrib><creatorcontrib>Jacob, Reuben P</creatorcontrib><creatorcontrib>Cohen, Cynthia</creatorcontrib><creatorcontrib>Siddiqui, Momin T</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><jtitle>Diagnostic cytopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simms, Anthony</au><au>Jacob, Reuben P</au><au>Cohen, Cynthia</au><au>Siddiqui, Momin T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TROP-2 expression in papillary thyroid carcinoma: Potential Diagnostic Utility</atitle><jtitle>Diagnostic cytopathology</jtitle><addtitle>Diagn Cytopathol</addtitle><date>2016-01</date><risdate>2016</risdate><volume>44</volume><issue>1</issue><spage>26</spage><epage>31</epage><pages>26-31</pages><issn>8755-1039</issn><eissn>1097-0339</eissn><abstract>TROP-2 is a type I transmembrane glycoprotein which is over-expressed in various malignancies, and is related to epithelial cell adhesion molecule (EpCAM), also called TROP-1, gp40, and KSA. In this study, we evaluated TROP-2 expression in papillary thyroid carcinoma (PTC) and compared it to other thyroid neoplastic and non-neoplastic lesions. Immunohistochemical (IHC) evaluation for TROP-2 was performed on 137 thyroid fine needle aspiration (FNA) cell blocks (CB) which included classic PTC (64), follicular variant PTC (FVPTC) (10), anaplastic thyroid carcinoma (AC) (2), medullary carcinoma (MC) (8), follicular neoplasms (FN) (8), Hurthle cell neoplasms (HCN) (9), follicular lesion of uncertain significance (FLUS) (12), and benign thyroid nodule (BTN) (24). IHC for TROP-2 expression was also performed on 331 BTN and malignant tumor tissue sections in tissue microarray (TMA). Membranous staining in >5% of tumor cells was considered positive. TROP-2 stained 61 of 64 PTC CB, 7 of 10 FVPTC CB, and 9 of 12 FLUS CB. All other cases were negative for TROP-2. TROP-2 showed a sensitivity of 95.31% and specificity of 89% for classic PTC in FNA CB. In TMA samples, TROP-2 stained 54 of 60 classic PTC cases and hence showed a high sensitivity and specificity. All BTN in CB and TMA were negative. We conclude that TROP-2 is a highly sensitive and specific IHC marker for identifying classic PTC. TROP-2 may play an important role in diagnosing classic PTC, especially in equivocal cases. This study also identifies a strong role for TROP-2 in separating PTC from BTN.</abstract><cop>United States</cop><pmid>26481593</pmid><doi>10.1002/dc.23382</doi><tpages>6</tpages></addata></record> |
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subjects | Adenocarcinoma, Follicular - diagnosis Adenocarcinoma, Follicular - genetics Adenocarcinoma, Follicular - pathology Antigens, Neoplasm - genetics Biomarkers, Tumor - genetics Biopsy, Fine-Needle Carcinoma - diagnosis Carcinoma - genetics Carcinoma - pathology Carcinoma, Medullary - diagnosis Carcinoma, Medullary - genetics Carcinoma, Medullary - pathology Carcinoma, Neuroendocrine - diagnosis Carcinoma, Neuroendocrine - genetics Carcinoma, Neuroendocrine - pathology Carcinoma, Papillary Cell Adhesion Molecules - genetics Diagnosis, Differential Gene Expression Humans Immunohistochemistry Retrospective Studies Sensitivity and Specificity Thyroid Carcinoma, Anaplastic - diagnosis Thyroid Carcinoma, Anaplastic - genetics Thyroid Carcinoma, Anaplastic - pathology Thyroid Neoplasms - diagnosis Thyroid Neoplasms - genetics Thyroid Neoplasms - pathology Thyroid Nodule - diagnosis Thyroid Nodule - genetics Thyroid Nodule - pathology Tissue Array Analysis |
title | TROP-2 expression in papillary thyroid carcinoma: Potential Diagnostic Utility |
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