HER2 molecular subtype is a dominant subtype of mammary Paget's cells. An immunohistochemical study

Sek P, Zawrocki A, Biernat W & Piekarski J H
(2010) Histopathology57, 564–571
HER2 molecular subtype is a dominant subtype of mammary Paget’s cells. An immunohistochemical study Aims:  To test the hypothesis that the similarity of the molecular subtypes of Paget’s cells to the molecular subtypes...

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Veröffentlicht in:Histopathology 2010-10, Vol.57 (4), p.564-571
Hauptverfasser: Sek, Piotr, Zawrocki, Antoni, Biernat, Wojciech, Piekarski, Janusz H
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container_title Histopathology
container_volume 57
creator Sek, Piotr
Zawrocki, Antoni
Biernat, Wojciech
Piekarski, Janusz H
description Sek P, Zawrocki A, Biernat W & Piekarski J H
(2010) Histopathology57, 564–571
HER2 molecular subtype is a dominant subtype of mammary Paget’s cells. An immunohistochemical study Aims:  To test the hypothesis that the similarity of the molecular subtypes of Paget’s cells to the molecular subtypes of the underlying breast carcinomas favours the epidermotrophic theory of the origin of Paget’s cells. Methods and results:  The immunohistochemical expression of markers that define particular molecular subtypes of breast carcinomas were analysed. The whole analysis was performed by means of tissue microarrays in mammary Paget’s disease and in the underlying breast carcinoma(s). Human epidermal growth factor receptor type 2 (HER2)‐overexpression subtype [oestrogen receptor (ER−); HER2+] was a dominant molecular subtype of Paget’s cells (37 of 43 analysed cases; 86%). Luminal B (ER+; HER2+) and luminal A (ER+; HER−) subtypes were identified in 12% and 2% of cases, respectively. None of the analysed tumours presented a basal‐like phenotype. A similar distribution of molecular subtypes was identified in the underlying in situ breast carcinomas (HER2 subtype, 82%; luminal A, 6%; luminal B, 6%; basal‐like, 6% of cases) and in the invasive component (HER2 subtype, 84%; luminal A, 8%; luminal B, 8%; basal‐like, 0% of cases). Conclusions:  HER2 molecular subtype is the dominant, but not the sole subtype seen in Paget’s cells of the nipple. A similar distribution of molecular subtypes in both Paget’s cells and in the underlying carcinomas strongly suggests their common origin.
doi_str_mv 10.1111/j.1365-2559.2010.03665.x
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(2010) Histopathology57, 564–571
HER2 molecular subtype is a dominant subtype of mammary Paget’s cells. An immunohistochemical study Aims:  To test the hypothesis that the similarity of the molecular subtypes of Paget’s cells to the molecular subtypes of the underlying breast carcinomas favours the epidermotrophic theory of the origin of Paget’s cells. Methods and results:  The immunohistochemical expression of markers that define particular molecular subtypes of breast carcinomas were analysed. The whole analysis was performed by means of tissue microarrays in mammary Paget’s disease and in the underlying breast carcinoma(s). Human epidermal growth factor receptor type 2 (HER2)‐overexpression subtype [oestrogen receptor (ER−); HER2+] was a dominant molecular subtype of Paget’s cells (37 of 43 analysed cases; 86%). Luminal B (ER+; HER2+) and luminal A (ER+; HER−) subtypes were identified in 12% and 2% of cases, respectively. None of the analysed tumours presented a basal‐like phenotype. A similar distribution of molecular subtypes was identified in the underlying in situ breast carcinomas (HER2 subtype, 82%; luminal A, 6%; luminal B, 6%; basal‐like, 6% of cases) and in the invasive component (HER2 subtype, 84%; luminal A, 8%; luminal B, 8%; basal‐like, 0% of cases). Conclusions:  HER2 molecular subtype is the dominant, but not the sole subtype seen in Paget’s cells of the nipple. A similar distribution of molecular subtypes in both Paget’s cells and in the underlying carcinomas strongly suggests their common origin.</description><identifier>ISSN: 0309-0167</identifier><identifier>EISSN: 1365-2559</identifier><identifier>DOI: 10.1111/j.1365-2559.2010.03665.x</identifier><identifier>PMID: 20955381</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Breast Neoplasms - classification ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Carcinoma, Ductal, Breast - classification ; Carcinoma, Ductal, Breast - genetics ; Carcinoma, Ductal, Breast - metabolism ; CK5/6 ; Diseases of the osteoarticular system ; Female ; HER2 ; Humans ; Immunohistochemistry ; Investigative techniques, diagnostic techniques (general aspects) ; mammary Paget's disease ; Medical sciences ; molecular subtype ; Osteoporosis. Osteomalacia. Paget disease ; Paget's Disease, Mammary - classification ; Paget's Disease, Mammary - genetics ; Paget's Disease, Mammary - metabolism ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Receptor, ErbB-2 - biosynthesis ; Receptor, ErbB-2 - genetics ; Receptors, Estrogen - biosynthesis ; Receptors, Estrogen - genetics ; Tissue Array Analysis ; tissue microarrays</subject><ispartof>Histopathology, 2010-10, Vol.57 (4), p.564-571</ispartof><rights>2010 Blackwell Publishing Limited</rights><rights>2015 INIST-CNRS</rights><rights>2010 Blackwell Publishing Limited.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5865-d962821d152b50bc0ba0a0816e2cf0c79fada1b81d89051cc181e0f1a22dd25e3</citedby><cites>FETCH-LOGICAL-c5865-d962821d152b50bc0ba0a0816e2cf0c79fada1b81d89051cc181e0f1a22dd25e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2559.2010.03665.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2559.2010.03665.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23351719$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20955381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00586993$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sek, Piotr</creatorcontrib><creatorcontrib>Zawrocki, Antoni</creatorcontrib><creatorcontrib>Biernat, Wojciech</creatorcontrib><creatorcontrib>Piekarski, Janusz H</creatorcontrib><title>HER2 molecular subtype is a dominant subtype of mammary Paget's cells. An immunohistochemical study</title><title>Histopathology</title><addtitle>Histopathology</addtitle><description>Sek P, Zawrocki A, Biernat W &amp; Piekarski J H
(2010) Histopathology57, 564–571
HER2 molecular subtype is a dominant subtype of mammary Paget’s cells. An immunohistochemical study Aims:  To test the hypothesis that the similarity of the molecular subtypes of Paget’s cells to the molecular subtypes of the underlying breast carcinomas favours the epidermotrophic theory of the origin of Paget’s cells. Methods and results:  The immunohistochemical expression of markers that define particular molecular subtypes of breast carcinomas were analysed. The whole analysis was performed by means of tissue microarrays in mammary Paget’s disease and in the underlying breast carcinoma(s). Human epidermal growth factor receptor type 2 (HER2)‐overexpression subtype [oestrogen receptor (ER−); HER2+] was a dominant molecular subtype of Paget’s cells (37 of 43 analysed cases; 86%). Luminal B (ER+; HER2+) and luminal A (ER+; HER−) subtypes were identified in 12% and 2% of cases, respectively. None of the analysed tumours presented a basal‐like phenotype. A similar distribution of molecular subtypes was identified in the underlying in situ breast carcinomas (HER2 subtype, 82%; luminal A, 6%; luminal B, 6%; basal‐like, 6% of cases) and in the invasive component (HER2 subtype, 84%; luminal A, 8%; luminal B, 8%; basal‐like, 0% of cases). Conclusions:  HER2 molecular subtype is the dominant, but not the sole subtype seen in Paget’s cells of the nipple. A similar distribution of molecular subtypes in both Paget’s cells and in the underlying carcinomas strongly suggests their common origin.</description><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - classification</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Carcinoma, Ductal, Breast - classification</subject><subject>Carcinoma, Ductal, Breast - genetics</subject><subject>Carcinoma, Ductal, Breast - metabolism</subject><subject>CK5/6</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>HER2</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>mammary Paget's disease</subject><subject>Medical sciences</subject><subject>molecular subtype</subject><subject>Osteoporosis. Osteomalacia. 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An immunohistochemical study</title><author>Sek, Piotr ; Zawrocki, Antoni ; Biernat, Wojciech ; Piekarski, Janusz H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5865-d962821d152b50bc0ba0a0816e2cf0c79fada1b81d89051cc181e0f1a22dd25e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biological and medical sciences</topic><topic>Breast Neoplasms - classification</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Carcinoma, Ductal, Breast - classification</topic><topic>Carcinoma, Ductal, Breast - genetics</topic><topic>Carcinoma, Ductal, Breast - metabolism</topic><topic>CK5/6</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>HER2</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>mammary Paget's disease</topic><topic>Medical sciences</topic><topic>molecular subtype</topic><topic>Osteoporosis. 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An immunohistochemical study</atitle><jtitle>Histopathology</jtitle><addtitle>Histopathology</addtitle><date>2010-10</date><risdate>2010</risdate><volume>57</volume><issue>4</issue><spage>564</spage><epage>571</epage><pages>564-571</pages><issn>0309-0167</issn><eissn>1365-2559</eissn><abstract>Sek P, Zawrocki A, Biernat W &amp; Piekarski J H
(2010) Histopathology57, 564–571
HER2 molecular subtype is a dominant subtype of mammary Paget’s cells. An immunohistochemical study Aims:  To test the hypothesis that the similarity of the molecular subtypes of Paget’s cells to the molecular subtypes of the underlying breast carcinomas favours the epidermotrophic theory of the origin of Paget’s cells. Methods and results:  The immunohistochemical expression of markers that define particular molecular subtypes of breast carcinomas were analysed. The whole analysis was performed by means of tissue microarrays in mammary Paget’s disease and in the underlying breast carcinoma(s). Human epidermal growth factor receptor type 2 (HER2)‐overexpression subtype [oestrogen receptor (ER−); HER2+] was a dominant molecular subtype of Paget’s cells (37 of 43 analysed cases; 86%). Luminal B (ER+; HER2+) and luminal A (ER+; HER−) subtypes were identified in 12% and 2% of cases, respectively. None of the analysed tumours presented a basal‐like phenotype. A similar distribution of molecular subtypes was identified in the underlying in situ breast carcinomas (HER2 subtype, 82%; luminal A, 6%; luminal B, 6%; basal‐like, 6% of cases) and in the invasive component (HER2 subtype, 84%; luminal A, 8%; luminal B, 8%; basal‐like, 0% of cases). Conclusions:  HER2 molecular subtype is the dominant, but not the sole subtype seen in Paget’s cells of the nipple. A similar distribution of molecular subtypes in both Paget’s cells and in the underlying carcinomas strongly suggests their common origin.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20955381</pmid><doi>10.1111/j.1365-2559.2010.03665.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Biological and medical sciences
Breast Neoplasms - classification
Breast Neoplasms - genetics
Breast Neoplasms - metabolism
Carcinoma, Ductal, Breast - classification
Carcinoma, Ductal, Breast - genetics
Carcinoma, Ductal, Breast - metabolism
CK5/6
Diseases of the osteoarticular system
Female
HER2
Humans
Immunohistochemistry
Investigative techniques, diagnostic techniques (general aspects)
mammary Paget's disease
Medical sciences
molecular subtype
Osteoporosis. Osteomalacia. Paget disease
Paget's Disease, Mammary - classification
Paget's Disease, Mammary - genetics
Paget's Disease, Mammary - metabolism
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Receptor, ErbB-2 - biosynthesis
Receptor, ErbB-2 - genetics
Receptors, Estrogen - biosynthesis
Receptors, Estrogen - genetics
Tissue Array Analysis
tissue microarrays
title HER2 molecular subtype is a dominant subtype of mammary Paget's cells. An immunohistochemical study
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