Localization of tumor‐associated glycoprotein DF3 in normal, inflammatory, and neoplastic lesions of the colon
Background. The expression of DF3 was assessed by a monoclonal antibody in normal, inflammatory, and neoplastic conditions in the large bowel. Methods. Using immunohistochemistry, expression was examined in formalin‐fixed paraffin‐embedded biopsy and resection samples of 19 normal colonic mucosal sp...
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Veröffentlicht in: | Cancer 1993-12, Vol.72 (11), p.3185-3190 |
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description | Background. The expression of DF3 was assessed by a monoclonal antibody in normal, inflammatory, and neoplastic conditions in the large bowel.
Methods. Using immunohistochemistry, expression was examined in formalin‐fixed paraffin‐embedded biopsy and resection samples of 19 normal colonic mucosal specimens, 49 inflammatory lesions, 34 adenomas, and 38 primary colonic adenocarcinomas. In addition, Western blots of normal colonic mucosa and adenocarcinoma were examined.
Results. DF3 expression was detected in 84% of the adenocarcinomas with coarse membrane staining, intense positivity of luminal secretions, and focal cytoplasmic and intracytoplasmic vacuole staining. Nine of 32 areas of transitional mucosa revealed reactivity along apical membranes in crypt cells. Five adenomas containing carcinoma revealed DF3 positivity in the malignant areas only, whereas the remaining 29 were negative. Staining was membrane, luminal, and intracytoplasmic. Two examples of active ulcerative colitis revealed focal reactivity along the apical membrane of crypt cells. No other areas of staining were noted, including 12 cases containing dysplasia. Four of 10 other inflammatory lesions also revealed similar membrane reactivity in crypt cells. Normal colonic mucosa was nonreactive. Examples of normal colonic mucosa were negative for DF3 by Western blot analysis, whereas two carcinoma samples that reacted immunohistochemically were positive.
Conclusions. DF3 is not detectable in normal colonic tissues. It is expressed focally and predominantly along the apical membrane of crypt cells in some inflammatory lesions and in the transitional mucosa of primary adenocarcinomas. Most adenocarcinomas of the colon and adenomas with foci of invasive carcinoma demonstrate reactivity in the cytoplasm and luminal secretions. |
doi_str_mv | 10.1002/1097-0142(19931201)72:11<3185::AID-CNCR2820721109>3.0.CO;2-7 |
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Methods. Using immunohistochemistry, expression was examined in formalin‐fixed paraffin‐embedded biopsy and resection samples of 19 normal colonic mucosal specimens, 49 inflammatory lesions, 34 adenomas, and 38 primary colonic adenocarcinomas. In addition, Western blots of normal colonic mucosa and adenocarcinoma were examined.
Results. DF3 expression was detected in 84% of the adenocarcinomas with coarse membrane staining, intense positivity of luminal secretions, and focal cytoplasmic and intracytoplasmic vacuole staining. Nine of 32 areas of transitional mucosa revealed reactivity along apical membranes in crypt cells. Five adenomas containing carcinoma revealed DF3 positivity in the malignant areas only, whereas the remaining 29 were negative. Staining was membrane, luminal, and intracytoplasmic. Two examples of active ulcerative colitis revealed focal reactivity along the apical membrane of crypt cells. No other areas of staining were noted, including 12 cases containing dysplasia. Four of 10 other inflammatory lesions also revealed similar membrane reactivity in crypt cells. Normal colonic mucosa was nonreactive. Examples of normal colonic mucosa were negative for DF3 by Western blot analysis, whereas two carcinoma samples that reacted immunohistochemically were positive.
Conclusions. DF3 is not detectable in normal colonic tissues. It is expressed focally and predominantly along the apical membrane of crypt cells in some inflammatory lesions and in the transitional mucosa of primary adenocarcinomas. Most adenocarcinomas of the colon and adenomas with foci of invasive carcinoma demonstrate reactivity in the cytoplasm and luminal secretions.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19931201)72:11<3185::AID-CNCR2820721109>3.0.CO;2-7</identifier><identifier>PMID: 7694786</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>adenocarcinoma ; Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adenoma - metabolism ; Adenoma - pathology ; adenomas ; antibodies ; Antibodies, Monoclonal ; antigens ; Antigens, Neoplasm - analysis ; Biological and medical sciences ; Biomarkers, Tumor - analysis ; Blotting, Western ; Carcinoma - metabolism ; Carcinoma - pathology ; Cell Transformation, Neoplastic - pathology ; Colitis - metabolism ; Colitis - pathology ; Colitis, Ulcerative - metabolism ; Colitis, Ulcerative - pathology ; colon ; Colon - cytology ; Colon - metabolism ; Colonic Neoplasms - metabolism ; Colonic Neoplasms - pathology ; Gastroenterology. Liver. Pancreas. Abdomen ; gastrointestinal neoplasia ; Gene Expression Regulation, Neoplastic ; human milk fat globule ; Humans ; Medical sciences ; monoclonal ; neoplasm ; Neoplasm Invasiveness ; Staining and Labeling ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer, 1993-12, Vol.72 (11), p.3185-3190</ispartof><rights>Copyright © 1993 American Cancer Society</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4169-3ad8cba938da4b5279cb81fc6d3326d10d93ab715805b96e9a6cf13683e9d5b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3880874$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7694786$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andrews, Charles W.</creatorcontrib><creatorcontrib>Jessup, J. Milburn</creatorcontrib><creatorcontrib>Goldman, Harvey</creatorcontrib><creatorcontrib>Hayes, Daniel F.</creatorcontrib><creatorcontrib>Kufe, Donald W.</creatorcontrib><creatorcontrib>O'Hara, Carl J.</creatorcontrib><creatorcontrib>Steele, Glenn D.</creatorcontrib><title>Localization of tumor‐associated glycoprotein DF3 in normal, inflammatory, and neoplastic lesions of the colon</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Background. The expression of DF3 was assessed by a monoclonal antibody in normal, inflammatory, and neoplastic conditions in the large bowel.
Methods. Using immunohistochemistry, expression was examined in formalin‐fixed paraffin‐embedded biopsy and resection samples of 19 normal colonic mucosal specimens, 49 inflammatory lesions, 34 adenomas, and 38 primary colonic adenocarcinomas. In addition, Western blots of normal colonic mucosa and adenocarcinoma were examined.
Results. DF3 expression was detected in 84% of the adenocarcinomas with coarse membrane staining, intense positivity of luminal secretions, and focal cytoplasmic and intracytoplasmic vacuole staining. Nine of 32 areas of transitional mucosa revealed reactivity along apical membranes in crypt cells. Five adenomas containing carcinoma revealed DF3 positivity in the malignant areas only, whereas the remaining 29 were negative. Staining was membrane, luminal, and intracytoplasmic. Two examples of active ulcerative colitis revealed focal reactivity along the apical membrane of crypt cells. No other areas of staining were noted, including 12 cases containing dysplasia. Four of 10 other inflammatory lesions also revealed similar membrane reactivity in crypt cells. Normal colonic mucosa was nonreactive. Examples of normal colonic mucosa were negative for DF3 by Western blot analysis, whereas two carcinoma samples that reacted immunohistochemically were positive.
Conclusions. DF3 is not detectable in normal colonic tissues. It is expressed focally and predominantly along the apical membrane of crypt cells in some inflammatory lesions and in the transitional mucosa of primary adenocarcinomas. Most adenocarcinomas of the colon and adenomas with foci of invasive carcinoma demonstrate reactivity in the cytoplasm and luminal secretions.</description><subject>adenocarcinoma</subject><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenoma - metabolism</subject><subject>Adenoma - pathology</subject><subject>adenomas</subject><subject>antibodies</subject><subject>Antibodies, Monoclonal</subject><subject>antigens</subject><subject>Antigens, Neoplasm - analysis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Blotting, Western</subject><subject>Carcinoma - metabolism</subject><subject>Carcinoma - pathology</subject><subject>Cell Transformation, Neoplastic - pathology</subject><subject>Colitis - metabolism</subject><subject>Colitis - pathology</subject><subject>Colitis, Ulcerative - metabolism</subject><subject>Colitis, Ulcerative - pathology</subject><subject>colon</subject><subject>Colon - cytology</subject><subject>Colon - metabolism</subject><subject>Colonic Neoplasms - metabolism</subject><subject>Colonic Neoplasms - pathology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>gastrointestinal neoplasia</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>human milk fat globule</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>monoclonal</subject><subject>neoplasm</subject><subject>Neoplasm Invasiveness</subject><subject>Staining and Labeling</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkd-K1DAUxoMo67r6CEIvRBS2Y07S5s8owtJxdWFwQBS8EMJpmq6VtBmbDjJe-Qg-o09ixhkH9ELw6pzwffn4OD9CFkBnQCl7AlTLnELBHoHWHBiFx5LNAZ5xUOV8fnG1yKvX1RumGJUMkvs5n9FZtXrKcnmDnB6_3ySnlFKVlwV_f5vcifFTekpW8hNyIoUupBKnZL0MFn33FacuDFlos2nTh_HHt-8YY7AdTq7Jrv3WhvUYJtcN2eKSZ2kMYezRn6e19dj3OIVxe57h0GSDC2uPceps5l1MqfFX7EeX2eDDcJfcatFHd-8wz8i7yxdvq1f5cvXyqrpY5rYAoXOOjbI1aq4aLOqSSW1rBa0VDedMNEAbzbGWUCpa1lo4jcK2wIXiTjdlTfkZebjPTcU_b1ycTN9F67zHVHATjRRUM2AiGT_sjXYMMY6uNeux63HcGqBmB8TsLmp2FzW_gRiZdjA7IMYkIOZPIIYbaqqVYUam-PuHHpu6d80x_EAg6Q8OOsZEoh1xsF082rhSVMki2a73ti-dd9v_rPjPhn8p_CcP2Ld0</recordid><startdate>19931201</startdate><enddate>19931201</enddate><creator>Andrews, Charles W.</creator><creator>Jessup, J. Milburn</creator><creator>Goldman, Harvey</creator><creator>Hayes, Daniel F.</creator><creator>Kufe, Donald W.</creator><creator>O'Hara, Carl J.</creator><creator>Steele, Glenn D.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><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>19931201</creationdate><title>Localization of tumor‐associated glycoprotein DF3 in normal, inflammatory, and neoplastic lesions of the colon</title><author>Andrews, Charles W. ; Jessup, J. Milburn ; Goldman, Harvey ; Hayes, Daniel F. ; Kufe, Donald W. ; O'Hara, Carl J. ; Steele, Glenn D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4169-3ad8cba938da4b5279cb81fc6d3326d10d93ab715805b96e9a6cf13683e9d5b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>adenocarcinoma</topic><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenoma - metabolism</topic><topic>Adenoma - pathology</topic><topic>adenomas</topic><topic>antibodies</topic><topic>Antibodies, Monoclonal</topic><topic>antigens</topic><topic>Antigens, Neoplasm - analysis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Blotting, Western</topic><topic>Carcinoma - metabolism</topic><topic>Carcinoma - pathology</topic><topic>Cell Transformation, Neoplastic - pathology</topic><topic>Colitis - metabolism</topic><topic>Colitis - pathology</topic><topic>Colitis, Ulcerative - metabolism</topic><topic>Colitis, Ulcerative - pathology</topic><topic>colon</topic><topic>Colon - cytology</topic><topic>Colon - metabolism</topic><topic>Colonic Neoplasms - metabolism</topic><topic>Colonic Neoplasms - pathology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>gastrointestinal neoplasia</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>human milk fat globule</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>monoclonal</topic><topic>neoplasm</topic><topic>Neoplasm Invasiveness</topic><topic>Staining and Labeling</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andrews, Charles W.</creatorcontrib><creatorcontrib>Jessup, J. Milburn</creatorcontrib><creatorcontrib>Goldman, Harvey</creatorcontrib><creatorcontrib>Hayes, Daniel F.</creatorcontrib><creatorcontrib>Kufe, Donald W.</creatorcontrib><creatorcontrib>O'Hara, Carl J.</creatorcontrib><creatorcontrib>Steele, Glenn D.</creatorcontrib><collection>Pascal-Francis</collection><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>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andrews, Charles W.</au><au>Jessup, J. Milburn</au><au>Goldman, Harvey</au><au>Hayes, Daniel F.</au><au>Kufe, Donald W.</au><au>O'Hara, Carl J.</au><au>Steele, Glenn D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localization of tumor‐associated glycoprotein DF3 in normal, inflammatory, and neoplastic lesions of the colon</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1993-12-01</date><risdate>1993</risdate><volume>72</volume><issue>11</issue><spage>3185</spage><epage>3190</epage><pages>3185-3190</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>Background. The expression of DF3 was assessed by a monoclonal antibody in normal, inflammatory, and neoplastic conditions in the large bowel.
Methods. Using immunohistochemistry, expression was examined in formalin‐fixed paraffin‐embedded biopsy and resection samples of 19 normal colonic mucosal specimens, 49 inflammatory lesions, 34 adenomas, and 38 primary colonic adenocarcinomas. In addition, Western blots of normal colonic mucosa and adenocarcinoma were examined.
Results. DF3 expression was detected in 84% of the adenocarcinomas with coarse membrane staining, intense positivity of luminal secretions, and focal cytoplasmic and intracytoplasmic vacuole staining. Nine of 32 areas of transitional mucosa revealed reactivity along apical membranes in crypt cells. Five adenomas containing carcinoma revealed DF3 positivity in the malignant areas only, whereas the remaining 29 were negative. Staining was membrane, luminal, and intracytoplasmic. Two examples of active ulcerative colitis revealed focal reactivity along the apical membrane of crypt cells. No other areas of staining were noted, including 12 cases containing dysplasia. Four of 10 other inflammatory lesions also revealed similar membrane reactivity in crypt cells. Normal colonic mucosa was nonreactive. Examples of normal colonic mucosa were negative for DF3 by Western blot analysis, whereas two carcinoma samples that reacted immunohistochemically were positive.
Conclusions. DF3 is not detectable in normal colonic tissues. It is expressed focally and predominantly along the apical membrane of crypt cells in some inflammatory lesions and in the transitional mucosa of primary adenocarcinomas. Most adenocarcinomas of the colon and adenomas with foci of invasive carcinoma demonstrate reactivity in the cytoplasm and luminal secretions.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7694786</pmid><doi>10.1002/1097-0142(19931201)72:11<3185::AID-CNCR2820721109>3.0.CO;2-7</doi><tpages>6</tpages></addata></record> |
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subjects | adenocarcinoma Adenocarcinoma - metabolism Adenocarcinoma - pathology Adenoma - metabolism Adenoma - pathology adenomas antibodies Antibodies, Monoclonal antigens Antigens, Neoplasm - analysis Biological and medical sciences Biomarkers, Tumor - analysis Blotting, Western Carcinoma - metabolism Carcinoma - pathology Cell Transformation, Neoplastic - pathology Colitis - metabolism Colitis - pathology Colitis, Ulcerative - metabolism Colitis, Ulcerative - pathology colon Colon - cytology Colon - metabolism Colonic Neoplasms - metabolism Colonic Neoplasms - pathology Gastroenterology. Liver. Pancreas. Abdomen gastrointestinal neoplasia Gene Expression Regulation, Neoplastic human milk fat globule Humans Medical sciences monoclonal neoplasm Neoplasm Invasiveness Staining and Labeling Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
title | Localization of tumor‐associated glycoprotein DF3 in normal, inflammatory, and neoplastic lesions of the colon |
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