Immunohistochemical localization of c-erbB-2 protein and epidermal growth factor receptor in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary

The c-erbB-2 (HER-2/neu) protein is a membrane glycoprotein growth factor receptor showing molecular homology with the epidermal growth factor receptor (EGFR). We examined the immunohistochemical reactivity of monoclonal antibodies against both of these proteins in normal surface epithelium, surface...

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Veröffentlicht in:Virchows Archiv A Pathological Anatomy and Histopathology 1992-09, Vol.421 (5), p.393-400
Hauptverfasser: Wang, D P, Konishi, I, Koshiyama, M, Nanbu, Y, Iwai, T, Nonogaki, H, Mori, T, Fujii, S
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container_issue 5
container_start_page 393
container_title Virchows Archiv A Pathological Anatomy and Histopathology
container_volume 421
creator Wang, D P
Konishi, I
Koshiyama, M
Nanbu, Y
Iwai, T
Nonogaki, H
Mori, T
Fujii, S
description The c-erbB-2 (HER-2/neu) protein is a membrane glycoprotein growth factor receptor showing molecular homology with the epidermal growth factor receptor (EGFR). We examined the immunohistochemical reactivity of monoclonal antibodies against both of these proteins in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary. The ovarian tumours were classified as benign (16), borderline malignant (2), and malignant (19). Normal surface ovarian epithelium was weakly positive for both c-erbB-2 protein and EGFR. In surface inclusion cysts, however, the epithelial cells lining the lumen exhibited stronger staining for c-erbB-2 protein, but no staining for EGFR. All 16 benign ovarian tumours and the 2 borderline malignant ovarian tumours were positive for c-erbB-2 protein and negative for EGFR. Of the ovarian carcinomas, 13 of the 19 (68.4%) were positive for c-erbB-2 protein and negative for EGFR, while 4 showed positivity for both c-erbB-2 protein and EGFR. Two cases were negative for both proteins. Expression of both c-erbB-2 protein and EGFR was found in endometrioid carcinoma with squamous differentiation and in clinically advanced poorly differentiated serous carcinomas. Expression of c-erbB-2 protein appears to be increased and that of EGFR is reduced in the early stage of epithelial ovarian oncogenesis. The expression of EGFR with c-erbB-2 protein in ovarian carcinoma is related both to histological differentiation and/or advanced clinical stage.
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We examined the immunohistochemical reactivity of monoclonal antibodies against both of these proteins in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary. The ovarian tumours were classified as benign (16), borderline malignant (2), and malignant (19). Normal surface ovarian epithelium was weakly positive for both c-erbB-2 protein and EGFR. In surface inclusion cysts, however, the epithelial cells lining the lumen exhibited stronger staining for c-erbB-2 protein, but no staining for EGFR. All 16 benign ovarian tumours and the 2 borderline malignant ovarian tumours were positive for c-erbB-2 protein and negative for EGFR. Of the ovarian carcinomas, 13 of the 19 (68.4%) were positive for c-erbB-2 protein and negative for EGFR, while 4 showed positivity for both c-erbB-2 protein and EGFR. Two cases were negative for both proteins. Expression of both c-erbB-2 protein and EGFR was found in endometrioid carcinoma with squamous differentiation and in clinically advanced poorly differentiated serous carcinomas. Expression of c-erbB-2 protein appears to be increased and that of EGFR is reduced in the early stage of epithelial ovarian oncogenesis. 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The expression of EGFR with c-erbB-2 protein in ovarian carcinoma is related both to histological differentiation and/or advanced clinical stage.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies, Monoclonal</subject><subject>Carcinoma - chemistry</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma - ultrastructure</subject><subject>Cell Transformation, Neoplastic - metabolism</subject><subject>Cell Transformation, Neoplastic - pathology</subject><subject>Epithelium - chemistry</subject><subject>Epithelium - pathology</subject><subject>Epithelium - ultrastructure</subject><subject>ErbB Receptors - analysis</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Middle Aged</subject><subject>Ovarian Cysts - chemistry</subject><subject>Ovarian Cysts - pathology</subject><subject>Ovarian Cysts - ultrastructure</subject><subject>Ovarian Neoplasms - chemistry</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Ovarian Neoplasms - ultrastructure</subject><subject>Ovary - chemistry</subject><subject>Ovary - pathology</subject><subject>Ovary - ultrastructure</subject><subject>Proto-Oncogene Proteins - analysis</subject><subject>Receptor, ErbB-2</subject><issn>0174-7398</issn><issn>1432-2307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUtv3SAQhVHVKrlJu-k-EqsuorgZjG3sZRPlJUXqpllbXBh6qYy55dEq-Wv5c8G5eWwYdObjMHAI-crgOwMQp2eXwDroBsY-kBVreF3VHMRHsgImmkrwod8nBzH-AWhb1rd7ZI_xDkQNK_J441ye_cbG5NUGnVVyopMvq32QyfqZekNVhWF9VtV0G3xCO1M5a4pbqzG4gv8O_n_aUCNV8oEGVLhdNoWb_TMQcyhNXI6kDU42u5M3zc5qynG5SN3HFE-evZV3riivfLFI2fkc4jJNkaj_J8P9Z_LJyCnil5d6SO4uL36dX1e3P69uzn_cVqru61TJbqg1mB6l5qbpOzQatAG9FqY1YAxXvVD9wFCgaXkj-BqULhKI8nO8afkh-bbzLc__mzGm0dmocJrkjD7HUXBei34YCni8A1XwMQY04zZYVyYdGYxLUuN7UgU-enHNa4f6Hd1Fw58A4hCTVQ</recordid><startdate>199209</startdate><enddate>199209</enddate><creator>Wang, D P</creator><creator>Konishi, I</creator><creator>Koshiyama, M</creator><creator>Nanbu, Y</creator><creator>Iwai, T</creator><creator>Nonogaki, H</creator><creator>Mori, T</creator><creator>Fujii, S</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>199209</creationdate><title>Immunohistochemical localization of c-erbB-2 protein and epidermal growth factor receptor in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary</title><author>Wang, D P ; Konishi, I ; Koshiyama, M ; Nanbu, Y ; Iwai, T ; Nonogaki, H ; Mori, T ; Fujii, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-a692d0f8ead3f486efd0df0db7f5f0ff3c87c891e7ef53473b0cd87c077393453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies, Monoclonal</topic><topic>Carcinoma - chemistry</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma - ultrastructure</topic><topic>Cell Transformation, Neoplastic - metabolism</topic><topic>Cell Transformation, Neoplastic - pathology</topic><topic>Epithelium - chemistry</topic><topic>Epithelium - pathology</topic><topic>Epithelium - ultrastructure</topic><topic>ErbB Receptors - analysis</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Middle Aged</topic><topic>Ovarian Cysts - chemistry</topic><topic>Ovarian Cysts - pathology</topic><topic>Ovarian Cysts - ultrastructure</topic><topic>Ovarian Neoplasms - chemistry</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Ovarian Neoplasms - ultrastructure</topic><topic>Ovary - chemistry</topic><topic>Ovary - pathology</topic><topic>Ovary - ultrastructure</topic><topic>Proto-Oncogene Proteins - analysis</topic><topic>Receptor, ErbB-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, D P</creatorcontrib><creatorcontrib>Konishi, I</creatorcontrib><creatorcontrib>Koshiyama, M</creatorcontrib><creatorcontrib>Nanbu, Y</creatorcontrib><creatorcontrib>Iwai, T</creatorcontrib><creatorcontrib>Nonogaki, H</creatorcontrib><creatorcontrib>Mori, T</creatorcontrib><creatorcontrib>Fujii, 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>MEDLINE - Academic</collection><jtitle>Virchows Archiv A Pathological Anatomy and Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, D P</au><au>Konishi, I</au><au>Koshiyama, M</au><au>Nanbu, Y</au><au>Iwai, T</au><au>Nonogaki, H</au><au>Mori, T</au><au>Fujii, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical localization of c-erbB-2 protein and epidermal growth factor receptor in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary</atitle><jtitle>Virchows Archiv A Pathological Anatomy and Histopathology</jtitle><addtitle>Virchows Arch A Pathol Anat Histopathol</addtitle><date>1992-09</date><risdate>1992</risdate><volume>421</volume><issue>5</issue><spage>393</spage><epage>400</epage><pages>393-400</pages><issn>0174-7398</issn><eissn>1432-2307</eissn><abstract>The c-erbB-2 (HER-2/neu) protein is a membrane glycoprotein growth factor receptor showing molecular homology with the epidermal growth factor receptor (EGFR). We examined the immunohistochemical reactivity of monoclonal antibodies against both of these proteins in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary. The ovarian tumours were classified as benign (16), borderline malignant (2), and malignant (19). Normal surface ovarian epithelium was weakly positive for both c-erbB-2 protein and EGFR. In surface inclusion cysts, however, the epithelial cells lining the lumen exhibited stronger staining for c-erbB-2 protein, but no staining for EGFR. All 16 benign ovarian tumours and the 2 borderline malignant ovarian tumours were positive for c-erbB-2 protein and negative for EGFR. Of the ovarian carcinomas, 13 of the 19 (68.4%) were positive for c-erbB-2 protein and negative for EGFR, while 4 showed positivity for both c-erbB-2 protein and EGFR. Two cases were negative for both proteins. Expression of both c-erbB-2 protein and EGFR was found in endometrioid carcinoma with squamous differentiation and in clinically advanced poorly differentiated serous carcinomas. Expression of c-erbB-2 protein appears to be increased and that of EGFR is reduced in the early stage of epithelial ovarian oncogenesis. The expression of EGFR with c-erbB-2 protein in ovarian carcinoma is related both to histological differentiation and/or advanced clinical stage.</abstract><cop>Germany</cop><pmid>1360720</pmid><doi>10.1007/BF01606911</doi><tpages>8</tpages></addata></record>
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ispartof Virchows Archiv A Pathological Anatomy and Histopathology, 1992-09, Vol.421 (5), p.393-400
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal
Carcinoma - chemistry
Carcinoma - pathology
Carcinoma - ultrastructure
Cell Transformation, Neoplastic - metabolism
Cell Transformation, Neoplastic - pathology
Epithelium - chemistry
Epithelium - pathology
Epithelium - ultrastructure
ErbB Receptors - analysis
Female
Humans
Immunohistochemistry
Middle Aged
Ovarian Cysts - chemistry
Ovarian Cysts - pathology
Ovarian Cysts - ultrastructure
Ovarian Neoplasms - chemistry
Ovarian Neoplasms - pathology
Ovarian Neoplasms - ultrastructure
Ovary - chemistry
Ovary - pathology
Ovary - ultrastructure
Proto-Oncogene Proteins - analysis
Receptor, ErbB-2
title Immunohistochemical localization of c-erbB-2 protein and epidermal growth factor receptor in normal surface epithelium, surface inclusion cysts, and common epithelial tumours of the ovary
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