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E-cadherin immunohistochemical expression in invasive lobular carcinoma of the breast: correlation with morphology and CDH1 somatic alterations
E-cadherin (ECAD) immunohistochemical (IHC) expression is lost in ∼90% of invasive lobular carcinomas (ILCs) owing to genomic alterations of CDH1. We examined morphologic features and ECAD IHC expression in invasive breast carcinomas (BCs) with known CDH1 alterations. Between January 2014 and May 20...
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Published in: | Human pathology 2020-08, Vol.102, p.44-53 |
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description | E-cadherin (ECAD) immunohistochemical (IHC) expression is lost in ∼90% of invasive lobular carcinomas (ILCs) owing to genomic alterations of CDH1. We examined morphologic features and ECAD IHC expression in invasive breast carcinomas (BCs) with known CDH1 alterations. Between January 2014 and May 2018, 202 cases of BC with a CDH1 somatic alteration were identified. ECAD expression was lost in 77% (155/202) of cases and was retained in 23% (47/202) cases. Most (90%, 139/155) ECAD-negative cases were morphologically classified as ILC, while the remaining (10%, 16/155) were invasive mammary carcinoma with mixed ductal and lobular features (IMC). Of 47 cases with ECAD staining, 62% (29/47) were classified as ILC, 23% (11/47) were classified as IMC, and 15% (7/47) were classified as invasive ductal carcinoma (IDC). Of note, 51% (24/47) of ECAD-positive cases were initially diagnosed as IDC or IMC based on ECAD expression alone. For ECAD-negative BCs, 98% (152/155) of CDH1 alterations were truncating, and 2% (3/155) were variants of unknown significance (VUS). Truncating CDH1 alterations were identified in the majority of ECAD-positive BCs (72%, 34/47); however, VUS-type CDH1 alterations were more prevalent (28%, 13/47) in ECAD-positive BCs than in ECAD-negative BCs. Although 90% of ECAD-negative tumors were compatible with ILC in this study, 17% (29/168) of ILC cases were ECAD positive. In addition, CDH1 truncating alterations were seen in ECAD-positive ILC, supporting the notion of aberrant ECAD staining. Therefore, ECAD IHC expression must be interpreted in conjunction with morphology, and BC with classic histologic features of ILC should not be reclassified as IDC/IMC based solely on the status of ECAD IHC expression.
•Lobular breast tumors show CDH1 alterations that impact E-cadherin expression.•Defective cadherin-catenin complexes likely result in aberrant E-cadherin staining.•Morphologically unequivocal lobular tumors can show aberrant E-cadherin staining.•E-cadherin expression must be interpreted in conjunction with tumor morphology.•Breast cancer classification should not be based solely on E-cadherin expression. |
doi_str_mv | 10.1016/j.humpath.2020.06.002 |
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•Lobular breast tumors show CDH1 alterations that impact E-cadherin expression.•Defective cadherin-catenin complexes likely result in aberrant E-cadherin staining.•Morphologically unequivocal lobular tumors can show aberrant E-cadherin staining.•E-cadherin expression must be interpreted in conjunction with tumor morphology.•Breast cancer classification should not be based solely on E-cadherin expression.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2020.06.002</identifier><identifier>PMID: 32599083</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antigens, CD - biosynthesis ; Antigens, CD - genetics ; Biomarkers, Tumor - analysis ; Breast cancer ; Breast Neoplasms - diagnosis ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Cadherins - biosynthesis ; Cadherins - genetics ; Carcinoma, Lobular - diagnosis ; Carcinoma, Lobular - genetics ; Carcinoma, Lobular - pathology ; CDH1 ; Cell adhesion & migration ; Chromosomes ; Cloning ; E-cadherin ; Female ; Gene Expression Regulation, Neoplastic - physiology ; Genes ; Genomes ; Humans ; Immunohistochemistry ; Laboratories ; Lobular ; Morphology ; Mutation ; p120 ; Proteins ; Tumors</subject><ispartof>Human pathology, 2020-08, Vol.102, p.44-53</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495t-7bdd9752b6e257ac788aeb74b3972866f5eee0d9872c54d1eda30ce17e15f6d23</citedby><cites>FETCH-LOGICAL-c495t-7bdd9752b6e257ac788aeb74b3972866f5eee0d9872c54d1eda30ce17e15f6d23</cites><orcidid>0000-0003-4610-0149 ; 0000-0001-9670-1810 ; 0000-0001-8419-6167</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32599083$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grabenstetter, Anne</creatorcontrib><creatorcontrib>Mohanty, Abhinita S.</creatorcontrib><creatorcontrib>Rana, Satshil</creatorcontrib><creatorcontrib>Zehir, Ahmet</creatorcontrib><creatorcontrib>Brannon, A. Rose</creatorcontrib><creatorcontrib>D'Alfonso, Timothy M.</creatorcontrib><creatorcontrib>DeLair, Deborah F.</creatorcontrib><creatorcontrib>Tan, Lee K.</creatorcontrib><creatorcontrib>Ross, Dara S.</creatorcontrib><title>E-cadherin immunohistochemical expression in invasive lobular carcinoma of the breast: correlation with morphology and CDH1 somatic alterations</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>E-cadherin (ECAD) immunohistochemical (IHC) expression is lost in ∼90% of invasive lobular carcinomas (ILCs) owing to genomic alterations of CDH1. We examined morphologic features and ECAD IHC expression in invasive breast carcinomas (BCs) with known CDH1 alterations. Between January 2014 and May 2018, 202 cases of BC with a CDH1 somatic alteration were identified. ECAD expression was lost in 77% (155/202) of cases and was retained in 23% (47/202) cases. Most (90%, 139/155) ECAD-negative cases were morphologically classified as ILC, while the remaining (10%, 16/155) were invasive mammary carcinoma with mixed ductal and lobular features (IMC). Of 47 cases with ECAD staining, 62% (29/47) were classified as ILC, 23% (11/47) were classified as IMC, and 15% (7/47) were classified as invasive ductal carcinoma (IDC). Of note, 51% (24/47) of ECAD-positive cases were initially diagnosed as IDC or IMC based on ECAD expression alone. For ECAD-negative BCs, 98% (152/155) of CDH1 alterations were truncating, and 2% (3/155) were variants of unknown significance (VUS). Truncating CDH1 alterations were identified in the majority of ECAD-positive BCs (72%, 34/47); however, VUS-type CDH1 alterations were more prevalent (28%, 13/47) in ECAD-positive BCs than in ECAD-negative BCs. Although 90% of ECAD-negative tumors were compatible with ILC in this study, 17% (29/168) of ILC cases were ECAD positive. In addition, CDH1 truncating alterations were seen in ECAD-positive ILC, supporting the notion of aberrant ECAD staining. Therefore, ECAD IHC expression must be interpreted in conjunction with morphology, and BC with classic histologic features of ILC should not be reclassified as IDC/IMC based solely on the status of ECAD IHC expression.
•Lobular breast tumors show CDH1 alterations that impact E-cadherin expression.•Defective cadherin-catenin complexes likely result in aberrant E-cadherin staining.•Morphologically unequivocal lobular tumors can show aberrant E-cadherin staining.•E-cadherin expression must be interpreted in conjunction with tumor morphology.•Breast cancer classification should not be based solely on E-cadherin expression.</description><subject>Antigens, CD - biosynthesis</subject><subject>Antigens, CD - genetics</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Cadherins - biosynthesis</subject><subject>Cadherins - genetics</subject><subject>Carcinoma, Lobular - diagnosis</subject><subject>Carcinoma, Lobular - genetics</subject><subject>Carcinoma, Lobular - pathology</subject><subject>CDH1</subject><subject>Cell adhesion & migration</subject><subject>Chromosomes</subject><subject>Cloning</subject><subject>E-cadherin</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic - physiology</subject><subject>Genes</subject><subject>Genomes</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Laboratories</subject><subject>Lobular</subject><subject>Morphology</subject><subject>Mutation</subject><subject>p120</subject><subject>Proteins</subject><subject>Tumors</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkc9u1DAQhyMEokvhEUCWuHBJ8N844QBC20KRKnGBs-XYk8arJF5sZ6FPwSvXYZcKuCBZ8mG-33jGX1E8J7gimNSvd9WwTHudhopiiitcVxjTB8WGCEbLhrX0YbHBmNdlQ6Q8K57EuMOYEMHF4-KMUdG2uGGb4udlabQdILgZuWlaZj-4mLwZYHJGjwh-7APE6Hwur-egozsAGn23jDogo4Nxs5808j1KA6AugI7pDTI-BBh1WoPfXRrQ5MN-8KO_uUV6tmh7cUVQzMHkDNJjgvCLjU-LR70eIzw73efF1w-XX7ZX5fXnj5-2769Lw1uRStlZ20pBuxqokNrIptHQSd6xVtKmrnsBANi2jaRGcEvAaoYNEAlE9LWl7Lx4e-y7X7oJrIE5BT2qfXCTDrfKa6f-rsxuUDf-oCRvOOdrg1enBsF_WyAmNbloYBz1DH6JinLS4pbVjGf05T_ozi9hzutlisnsiok6U-JImeBjDNDfD0OwWpWrnTopV6tyhWuVlefciz83uU_9dpyBd0cA8n8eHAQVjYPZgHUBTFLWu_88cQcwRsRu</recordid><startdate>20200801</startdate><enddate>20200801</enddate><creator>Grabenstetter, Anne</creator><creator>Mohanty, Abhinita S.</creator><creator>Rana, Satshil</creator><creator>Zehir, Ahmet</creator><creator>Brannon, A. Rose</creator><creator>D'Alfonso, Timothy M.</creator><creator>DeLair, Deborah F.</creator><creator>Tan, Lee K.</creator><creator>Ross, Dara S.</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4610-0149</orcidid><orcidid>https://orcid.org/0000-0001-9670-1810</orcidid><orcidid>https://orcid.org/0000-0001-8419-6167</orcidid></search><sort><creationdate>20200801</creationdate><title>E-cadherin immunohistochemical expression in invasive lobular carcinoma of the breast: correlation with morphology and CDH1 somatic alterations</title><author>Grabenstetter, Anne ; Mohanty, Abhinita S. ; Rana, Satshil ; Zehir, Ahmet ; Brannon, A. Rose ; D'Alfonso, Timothy M. ; DeLair, Deborah F. ; Tan, Lee K. ; Ross, Dara S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c495t-7bdd9752b6e257ac788aeb74b3972866f5eee0d9872c54d1eda30ce17e15f6d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antigens, CD - biosynthesis</topic><topic>Antigens, CD - genetics</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Cadherins - biosynthesis</topic><topic>Cadherins - genetics</topic><topic>Carcinoma, Lobular - diagnosis</topic><topic>Carcinoma, Lobular - genetics</topic><topic>Carcinoma, Lobular - pathology</topic><topic>CDH1</topic><topic>Cell adhesion & migration</topic><topic>Chromosomes</topic><topic>Cloning</topic><topic>E-cadherin</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic - physiology</topic><topic>Genes</topic><topic>Genomes</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Laboratories</topic><topic>Lobular</topic><topic>Morphology</topic><topic>Mutation</topic><topic>p120</topic><topic>Proteins</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grabenstetter, Anne</creatorcontrib><creatorcontrib>Mohanty, Abhinita S.</creatorcontrib><creatorcontrib>Rana, Satshil</creatorcontrib><creatorcontrib>Zehir, Ahmet</creatorcontrib><creatorcontrib>Brannon, A. Rose</creatorcontrib><creatorcontrib>D'Alfonso, Timothy M.</creatorcontrib><creatorcontrib>DeLair, Deborah F.</creatorcontrib><creatorcontrib>Tan, Lee K.</creatorcontrib><creatorcontrib>Ross, Dara S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grabenstetter, Anne</au><au>Mohanty, Abhinita S.</au><au>Rana, Satshil</au><au>Zehir, Ahmet</au><au>Brannon, A. Rose</au><au>D'Alfonso, Timothy M.</au><au>DeLair, Deborah F.</au><au>Tan, Lee K.</au><au>Ross, Dara S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>E-cadherin immunohistochemical expression in invasive lobular carcinoma of the breast: correlation with morphology and CDH1 somatic alterations</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2020-08-01</date><risdate>2020</risdate><volume>102</volume><spage>44</spage><epage>53</epage><pages>44-53</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>E-cadherin (ECAD) immunohistochemical (IHC) expression is lost in ∼90% of invasive lobular carcinomas (ILCs) owing to genomic alterations of CDH1. We examined morphologic features and ECAD IHC expression in invasive breast carcinomas (BCs) with known CDH1 alterations. Between January 2014 and May 2018, 202 cases of BC with a CDH1 somatic alteration were identified. ECAD expression was lost in 77% (155/202) of cases and was retained in 23% (47/202) cases. Most (90%, 139/155) ECAD-negative cases were morphologically classified as ILC, while the remaining (10%, 16/155) were invasive mammary carcinoma with mixed ductal and lobular features (IMC). Of 47 cases with ECAD staining, 62% (29/47) were classified as ILC, 23% (11/47) were classified as IMC, and 15% (7/47) were classified as invasive ductal carcinoma (IDC). Of note, 51% (24/47) of ECAD-positive cases were initially diagnosed as IDC or IMC based on ECAD expression alone. For ECAD-negative BCs, 98% (152/155) of CDH1 alterations were truncating, and 2% (3/155) were variants of unknown significance (VUS). Truncating CDH1 alterations were identified in the majority of ECAD-positive BCs (72%, 34/47); however, VUS-type CDH1 alterations were more prevalent (28%, 13/47) in ECAD-positive BCs than in ECAD-negative BCs. Although 90% of ECAD-negative tumors were compatible with ILC in this study, 17% (29/168) of ILC cases were ECAD positive. In addition, CDH1 truncating alterations were seen in ECAD-positive ILC, supporting the notion of aberrant ECAD staining. Therefore, ECAD IHC expression must be interpreted in conjunction with morphology, and BC with classic histologic features of ILC should not be reclassified as IDC/IMC based solely on the status of ECAD IHC expression.
•Lobular breast tumors show CDH1 alterations that impact E-cadherin expression.•Defective cadherin-catenin complexes likely result in aberrant E-cadherin staining.•Morphologically unequivocal lobular tumors can show aberrant E-cadherin staining.•E-cadherin expression must be interpreted in conjunction with tumor morphology.•Breast cancer classification should not be based solely on E-cadherin expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32599083</pmid><doi>10.1016/j.humpath.2020.06.002</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4610-0149</orcidid><orcidid>https://orcid.org/0000-0001-9670-1810</orcidid><orcidid>https://orcid.org/0000-0001-8419-6167</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, CD - biosynthesis Antigens, CD - genetics Biomarkers, Tumor - analysis Breast cancer Breast Neoplasms - diagnosis Breast Neoplasms - genetics Breast Neoplasms - pathology Cadherins - biosynthesis Cadherins - genetics Carcinoma, Lobular - diagnosis Carcinoma, Lobular - genetics Carcinoma, Lobular - pathology CDH1 Cell adhesion & migration Chromosomes Cloning E-cadherin Female Gene Expression Regulation, Neoplastic - physiology Genes Genomes Humans Immunohistochemistry Laboratories Lobular Morphology Mutation p120 Proteins Tumors |
title | E-cadherin immunohistochemical expression in invasive lobular carcinoma of the breast: correlation with morphology and CDH1 somatic alterations |
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