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Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors

INTRODUCTION: Trophoblast cell surface antigen 2 (TROP2) is the target of sacituzumab govitecan, an antibody-drug conjugate approved for treatment of triple negative breast cancer and urothelial carcinoma. METHODS: A tissue microarray containing 18,563 samples from 150 different tumor types and subt...

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Autores principales: Dum, David, Taherpour, Noushin, Menz, Anne, Höflmayer, Doris, Völkel, Cosima, Hinsch, Andrea, Gorbokon, Natalia, Lennartz, Maximilian, Hube-Magg, Claudia, Fraune, Christoph, Bernreuther, Christian, Lebok, Patrick, Clauditz, Till S., Jacobsen, Frank, Sauter, Guido, Uhlig, Ria, Wilczak, Waldemar, Steurer, Stefan, Minner, Sarah, Marx, Andreas H., Simon, Ronald, Burandt, Eike, Krech, Till, Luebke, Andreas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393818/
https://www.ncbi.nlm.nih.gov/pubmed/35477165
http://dx.doi.org/10.1159/000522206
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author Dum, David
Taherpour, Noushin
Menz, Anne
Höflmayer, Doris
Völkel, Cosima
Hinsch, Andrea
Gorbokon, Natalia
Lennartz, Maximilian
Hube-Magg, Claudia
Fraune, Christoph
Bernreuther, Christian
Lebok, Patrick
Clauditz, Till S.
Jacobsen, Frank
Sauter, Guido
Uhlig, Ria
Wilczak, Waldemar
Steurer, Stefan
Minner, Sarah
Marx, Andreas H.
Simon, Ronald
Burandt, Eike
Krech, Till
Luebke, Andreas M.
author_facet Dum, David
Taherpour, Noushin
Menz, Anne
Höflmayer, Doris
Völkel, Cosima
Hinsch, Andrea
Gorbokon, Natalia
Lennartz, Maximilian
Hube-Magg, Claudia
Fraune, Christoph
Bernreuther, Christian
Lebok, Patrick
Clauditz, Till S.
Jacobsen, Frank
Sauter, Guido
Uhlig, Ria
Wilczak, Waldemar
Steurer, Stefan
Minner, Sarah
Marx, Andreas H.
Simon, Ronald
Burandt, Eike
Krech, Till
Luebke, Andreas M.
author_sort Dum, David
collection PubMed
description INTRODUCTION: Trophoblast cell surface antigen 2 (TROP2) is the target of sacituzumab govitecan, an antibody-drug conjugate approved for treatment of triple negative breast cancer and urothelial carcinoma. METHODS: A tissue microarray containing 18,563 samples from 150 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by TROP2 immunohistochemistry. RESULTS: TROP2 positivity was found in 109 tumor categories, including squamous cell carcinomas of various origins, urothelial, breast, prostate, pancreatic, and ovarian cancers (>95% positive). High TROP2 expression was linked to advanced stage (p = 0.0069) and nodal metastasis (p < 0.0001) in colorectal cancer as well as to nodal metastasis in gastric adenocarcinoma (p = 0.0246) and papillary thyroid cancer (p = 0.0013). Low TROP2 expression was linked to advanced stage in urothelial carcinoma (p < 0.0001), high pT (p = 0.0024), and high grade (p < 0.0001) in breast cancer, as well as with high Fuhrmann grade (p < 0.0001) and pT stage (p = 0.0009) in papillary renal cell carcinomas. CONCLUSION: TROP2 is expressed in many epithelial neoplasms. TROP2 deregulation can be associated with cancer progression in a tumor-type dependent manner. Since anti-TROP2 cancer drugs have demonstrated efficiency, they may be applicable to a broad range of tumor entities in the future.
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spelling pubmed-93938182022-09-23 Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors Dum, David Taherpour, Noushin Menz, Anne Höflmayer, Doris Völkel, Cosima Hinsch, Andrea Gorbokon, Natalia Lennartz, Maximilian Hube-Magg, Claudia Fraune, Christoph Bernreuther, Christian Lebok, Patrick Clauditz, Till S. Jacobsen, Frank Sauter, Guido Uhlig, Ria Wilczak, Waldemar Steurer, Stefan Minner, Sarah Marx, Andreas H. Simon, Ronald Burandt, Eike Krech, Till Luebke, Andreas M. Pathobiology Research Article INTRODUCTION: Trophoblast cell surface antigen 2 (TROP2) is the target of sacituzumab govitecan, an antibody-drug conjugate approved for treatment of triple negative breast cancer and urothelial carcinoma. METHODS: A tissue microarray containing 18,563 samples from 150 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by TROP2 immunohistochemistry. RESULTS: TROP2 positivity was found in 109 tumor categories, including squamous cell carcinomas of various origins, urothelial, breast, prostate, pancreatic, and ovarian cancers (>95% positive). High TROP2 expression was linked to advanced stage (p = 0.0069) and nodal metastasis (p < 0.0001) in colorectal cancer as well as to nodal metastasis in gastric adenocarcinoma (p = 0.0246) and papillary thyroid cancer (p = 0.0013). Low TROP2 expression was linked to advanced stage in urothelial carcinoma (p < 0.0001), high pT (p = 0.0024), and high grade (p < 0.0001) in breast cancer, as well as with high Fuhrmann grade (p < 0.0001) and pT stage (p = 0.0009) in papillary renal cell carcinomas. CONCLUSION: TROP2 is expressed in many epithelial neoplasms. TROP2 deregulation can be associated with cancer progression in a tumor-type dependent manner. Since anti-TROP2 cancer drugs have demonstrated efficiency, they may be applicable to a broad range of tumor entities in the future. S. Karger AG 2022-04-27 /pmc/articles/PMC9393818/ /pubmed/35477165 http://dx.doi.org/10.1159/000522206 Text en The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
spellingShingle Research Article
Dum, David
Taherpour, Noushin
Menz, Anne
Höflmayer, Doris
Völkel, Cosima
Hinsch, Andrea
Gorbokon, Natalia
Lennartz, Maximilian
Hube-Magg, Claudia
Fraune, Christoph
Bernreuther, Christian
Lebok, Patrick
Clauditz, Till S.
Jacobsen, Frank
Sauter, Guido
Uhlig, Ria
Wilczak, Waldemar
Steurer, Stefan
Minner, Sarah
Marx, Andreas H.
Simon, Ronald
Burandt, Eike
Krech, Till
Luebke, Andreas M.
Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title_full Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title_fullStr Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title_full_unstemmed Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title_short Trophoblast Cell Surface Antigen 2 Expression in Human Tumors: A Tissue Microarray Study on 18,563 Tumors
title_sort trophoblast cell surface antigen 2 expression in human tumors: a tissue microarray study on 18,563 tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393818/
https://www.ncbi.nlm.nih.gov/pubmed/35477165
http://dx.doi.org/10.1159/000522206
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