Cadherin-17 (CDH17) expression in human cancer: A tissue microarray study on 18,131 tumors
Cadherin-17 (CDH17) is a membranous cell adhesion protein predominantly expressed in intestinal epithelial cells. CDH17 is therefore considered a possible diagnostic and therapeutic target. This study was to comprehensively determine the expression of CDH17 in cancer and to further assess the diagno...
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creator | Jacobsen, Frank Pushpadevan, Ramesh Viehweger, Florian Freytag, Morton Schlichter, Ria Gorbokon, Natalia Büscheck, Franziska Luebke, Andreas M. Putri, Devita Kluth, Martina Hube-Magg, Claudia Hinsch, Andrea Höflmayer, Doris Fraune, Christoph Bernreuther, Christian Lebok, Patrick Sauter, Guido Minner, Sarah Steurer, Stefan Simon, Ronald Burandt, Eike Dum, David Lutz, Florian Marx, Andreas H. Krech, Till Clauditz, Till S. |
description | Cadherin-17 (CDH17) is a membranous cell adhesion protein predominantly expressed in intestinal epithelial cells. CDH17 is therefore considered a possible diagnostic and therapeutic target. This study was to comprehensively determine the expression of CDH17 in cancer and to further assess the diagnostic utility of CDH17 immunohistochemistry (IHC). A tissue microarray containing 14,948 interpretable samples from 150 different tumor types and subtypes as well as 76 different normal tissue types was analyzed by IHC. In normal tissues, a membranous CDH17 staining was predominantly seen in the epithelium of the intestine and pancreatic excretory ducts. In tumors, 53 of 150 analyzed categories showed CDH17 positivity including 26 categories with at least one strongly positive case. CDH17 positivity was most common in epithelial and neuroendocrine colorectal neoplasms (50.0%−100%), other gastrointestinal adenocarcinomas (42.7%−61.6%), mucinous ovarian cancer (61.1%), pancreatic acinar cell carcinoma (28.6%), cervical adenocarcinoma (52.6%), bilio-pancreatic adenocarcinomas (40.5–69.8%), and other neuroendocrine neoplasms (5.6%−100%). OnIy 9.9% of 182 pulmonary adenocarcinomas were CDH17 positive. In colorectal adenocarcinomas, reduced CDH17 staining was linked to high pT (p = 0.0147), nodal metastasis (p = 0.0041), V1 (p = 0.0025), L1 (p = 0.0054), location in the right colon (p = 0.0033), and microsatellite instability (p |
doi_str_mv | 10.1016/j.prp.2024.155175 |
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CDH17 is therefore considered a possible diagnostic and therapeutic target. This study was to comprehensively determine the expression of CDH17 in cancer and to further assess the diagnostic utility of CDH17 immunohistochemistry (IHC). A tissue microarray containing 14,948 interpretable samples from 150 different tumor types and subtypes as well as 76 different normal tissue types was analyzed by IHC. In normal tissues, a membranous CDH17 staining was predominantly seen in the epithelium of the intestine and pancreatic excretory ducts. In tumors, 53 of 150 analyzed categories showed CDH17 positivity including 26 categories with at least one strongly positive case. CDH17 positivity was most common in epithelial and neuroendocrine colorectal neoplasms (50.0%−100%), other gastrointestinal adenocarcinomas (42.7%−61.6%), mucinous ovarian cancer (61.1%), pancreatic acinar cell carcinoma (28.6%), cervical adenocarcinoma (52.6%), bilio-pancreatic adenocarcinomas (40.5–69.8%), and other neuroendocrine neoplasms (5.6%−100%). OnIy 9.9% of 182 pulmonary adenocarcinomas were CDH17 positive. In colorectal adenocarcinomas, reduced CDH17 staining was linked to high pT (p = 0.0147), nodal metastasis (p = 0.0041), V1 (p = 0.0025), L1 (p = 0.0054), location in the right colon (p = 0.0033), and microsatellite instability (p < 0.0001). The CDH17 expression level was unrelated to tumor phenotype in gastric and pancreatic cancer. In summary, our comprehensive overview on CDH17 expression in human tumors identified various tumor entities that might often benefit from anti-CDH17 therapies and suggest utility of CDH17 IHC for the distinction of metastatic gastrointestinal or bilio-pancreatic adenocarcinomas (often positive) from primary pulmonary adenocarcinomas (mostly negative).</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2024.155175</identifier><identifier>PMID: 38452580</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><ispartof>Pathology, research and practice, 2024-04, Vol.256, p.155175-155175, Article 155175</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier GmbH.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-7d28f50e490cadc3a9da860447deb66160834c1f4f1456c9a2fbfdfe7736c5e53</citedby><cites>FETCH-LOGICAL-c396t-7d28f50e490cadc3a9da860447deb66160834c1f4f1456c9a2fbfdfe7736c5e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.prp.2024.155175$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38452580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jacobsen, Frank</creatorcontrib><creatorcontrib>Pushpadevan, Ramesh</creatorcontrib><creatorcontrib>Viehweger, Florian</creatorcontrib><creatorcontrib>Freytag, Morton</creatorcontrib><creatorcontrib>Schlichter, Ria</creatorcontrib><creatorcontrib>Gorbokon, Natalia</creatorcontrib><creatorcontrib>Büscheck, Franziska</creatorcontrib><creatorcontrib>Luebke, Andreas M.</creatorcontrib><creatorcontrib>Putri, Devita</creatorcontrib><creatorcontrib>Kluth, Martina</creatorcontrib><creatorcontrib>Hube-Magg, Claudia</creatorcontrib><creatorcontrib>Hinsch, Andrea</creatorcontrib><creatorcontrib>Höflmayer, Doris</creatorcontrib><creatorcontrib>Fraune, Christoph</creatorcontrib><creatorcontrib>Bernreuther, Christian</creatorcontrib><creatorcontrib>Lebok, Patrick</creatorcontrib><creatorcontrib>Sauter, Guido</creatorcontrib><creatorcontrib>Minner, Sarah</creatorcontrib><creatorcontrib>Steurer, Stefan</creatorcontrib><creatorcontrib>Simon, Ronald</creatorcontrib><creatorcontrib>Burandt, Eike</creatorcontrib><creatorcontrib>Dum, David</creatorcontrib><creatorcontrib>Lutz, Florian</creatorcontrib><creatorcontrib>Marx, Andreas H.</creatorcontrib><creatorcontrib>Krech, Till</creatorcontrib><creatorcontrib>Clauditz, Till S.</creatorcontrib><title>Cadherin-17 (CDH17) expression in human cancer: A tissue microarray study on 18,131 tumors</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>Cadherin-17 (CDH17) is a membranous cell adhesion protein predominantly expressed in intestinal epithelial cells. CDH17 is therefore considered a possible diagnostic and therapeutic target. This study was to comprehensively determine the expression of CDH17 in cancer and to further assess the diagnostic utility of CDH17 immunohistochemistry (IHC). A tissue microarray containing 14,948 interpretable samples from 150 different tumor types and subtypes as well as 76 different normal tissue types was analyzed by IHC. In normal tissues, a membranous CDH17 staining was predominantly seen in the epithelium of the intestine and pancreatic excretory ducts. In tumors, 53 of 150 analyzed categories showed CDH17 positivity including 26 categories with at least one strongly positive case. CDH17 positivity was most common in epithelial and neuroendocrine colorectal neoplasms (50.0%−100%), other gastrointestinal adenocarcinomas (42.7%−61.6%), mucinous ovarian cancer (61.1%), pancreatic acinar cell carcinoma (28.6%), cervical adenocarcinoma (52.6%), bilio-pancreatic adenocarcinomas (40.5–69.8%), and other neuroendocrine neoplasms (5.6%−100%). OnIy 9.9% of 182 pulmonary adenocarcinomas were CDH17 positive. In colorectal adenocarcinomas, reduced CDH17 staining was linked to high pT (p = 0.0147), nodal metastasis (p = 0.0041), V1 (p = 0.0025), L1 (p = 0.0054), location in the right colon (p = 0.0033), and microsatellite instability (p < 0.0001). The CDH17 expression level was unrelated to tumor phenotype in gastric and pancreatic cancer. 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CDH17 is therefore considered a possible diagnostic and therapeutic target. This study was to comprehensively determine the expression of CDH17 in cancer and to further assess the diagnostic utility of CDH17 immunohistochemistry (IHC). A tissue microarray containing 14,948 interpretable samples from 150 different tumor types and subtypes as well as 76 different normal tissue types was analyzed by IHC. In normal tissues, a membranous CDH17 staining was predominantly seen in the epithelium of the intestine and pancreatic excretory ducts. In tumors, 53 of 150 analyzed categories showed CDH17 positivity including 26 categories with at least one strongly positive case. CDH17 positivity was most common in epithelial and neuroendocrine colorectal neoplasms (50.0%−100%), other gastrointestinal adenocarcinomas (42.7%−61.6%), mucinous ovarian cancer (61.1%), pancreatic acinar cell carcinoma (28.6%), cervical adenocarcinoma (52.6%), bilio-pancreatic adenocarcinomas (40.5–69.8%), and other neuroendocrine neoplasms (5.6%−100%). OnIy 9.9% of 182 pulmonary adenocarcinomas were CDH17 positive. In colorectal adenocarcinomas, reduced CDH17 staining was linked to high pT (p = 0.0147), nodal metastasis (p = 0.0041), V1 (p = 0.0025), L1 (p = 0.0054), location in the right colon (p = 0.0033), and microsatellite instability (p < 0.0001). The CDH17 expression level was unrelated to tumor phenotype in gastric and pancreatic cancer. In summary, our comprehensive overview on CDH17 expression in human tumors identified various tumor entities that might often benefit from anti-CDH17 therapies and suggest utility of CDH17 IHC for the distinction of metastatic gastrointestinal or bilio-pancreatic adenocarcinomas (often positive) from primary pulmonary adenocarcinomas (mostly negative).</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>38452580</pmid><doi>10.1016/j.prp.2024.155175</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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title | Cadherin-17 (CDH17) expression in human cancer: A tissue microarray study on 18,131 tumors |
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