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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
Main Authors: 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.
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creator Grabenstetter, Anne
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Tan, Lee K.
Ross, Dara S.
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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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><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 &amp; 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. 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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. 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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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source ScienceDirect Freedom Collection 2022-2024
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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