Cadherin-17 (CDH17) expression in human cancer: A tissue microarray study on 18,131 tumors

钙粘蛋白 免疫组织化学 组织微阵列 癌症 腺癌 癌症研究 生物 病理 医学 细胞 遗传学 免疫学
作者
Frank Jacobsen,Ramesh Pushpadevan,Florian Viehweger,Morton Freytag,Ria Schlichter,Natalia Gorbokon,Franziska Büscheck,Andreas M. Luebke,Devita Putri,Martina Kluth,Claudia Hube‐Magg,Andrea Hinsch,Doris Höflmayer,Christoph Fraune,Christian Bernreuther,Patrick Lebok,Guido Sauter,Sarah Minner,Stefan Steurer,Ronald Simon
出处
期刊:Pathology Research and Practice [Elsevier BV]
卷期号:256: 155175-155175 被引量:16
标识
DOI:10.1016/j.prp.2024.155175
摘要

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. 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).
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