Cytokeratin 13 (CK13) Expression in Cancer: A Tissue Microarray Study on 10,439 Tumors

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@article{dbb33890906c4628ba691c5ccb4317a7,
title = "Cytokeratin 13 (CK13) Expression in Cancer: A Tissue Microarray Study on 10,439 Tumors",
abstract = "Cytokeratin 13 (CK13) is a type I acidic low molecular weight cytokeratin, which is mainly expressed in urothelium and in the squamous epithelium of various sites of origin. Loss of CK13 has been implicated in the development and progression of squamous epithelial neoplasms. To comprehensively determine CK13 expression in normal and neoplastic tissues, a tissue microarray containing 10,439 samples from 131 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. CK13 immunostaining was detectable in 42 (32.1%) of the 131 tumor categories including 24 (18.3%) tumor types with at least one strongly positive case. The highest rate of positive staining was found in various urothelial neoplasms (52.1-92.3%) including Brenner tumor of the ovary (86.8%) and in squamous cell carcinomas from various sites of origin (39.1-77.6%), Warthin tumors of parotid glands (66.7%), adenosquamous carcinomas of the cervix (33.3%), thymomas (16.0%), and endometroid carcinomas of the ovary (15.3%). Twenty other epithelial or germ cell neoplasms showed - a usually weak - CK13 positivity in less than 15% of the cases. In bladder cancer, reduced CK13 expression was linked to high grade and advanced stage (p < 0.0001 each). In squamous cell carcinoma of the cervix, reduced CK13 immunostaining was related to high grade (p = 0.0295) and shortened recurrence-free (p = 0.0094) and overall survival (p = 0.0274). In a combined analysis of 1,151 squamous cell carcinomas from 11 different sites of origin, reduced CK13 staining was linked to high grade (p = 0.0050). Our data provide a comprehensive overview on CK13 expression in normal and neoplastic human tissues. CK13 expression predominates in urothelial neoplasms and in squamous cell carcinomas of different organs, and a loss of CK13 expression is associated with aggressive disease in these tumors.",
author = "Maximilian Lennartz and Ullmann, {Verena Sofia} and Natalia Gorbokon and Ria Uhlig and {Dwertmann Rico}, Sebastian and Simon Kind and Viktor Reiswich and Florian Viehweger and Martina Kluth and Claudia Hube-Magg and Christian Bernreuther and Franziska B{\"u}scheck and Devita Putri and Clauditz, {Till S} and Christoph Fraune and Andrea Hinsch and Frank Jacobsen and Till Krech and Patrick Lebock and Stefan Steurer and Eike Burandt and Sarah Minner and Marx, {Andreas H} and Ronald Simon and Guido Sauter and Anne Menz",
note = "This article is protected by copyright. All rights reserved.",
year = "2023",
month = feb,
doi = "10.1111/apm.13280",
language = "English",
volume = "131",
pages = "77--91",
journal = "APMIS",
issn = "0903-4641",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Cytokeratin 13 (CK13) Expression in Cancer: A Tissue Microarray Study on 10,439 Tumors

AU - Lennartz, Maximilian

AU - Ullmann, Verena Sofia

AU - Gorbokon, Natalia

AU - Uhlig, Ria

AU - Dwertmann Rico, Sebastian

AU - Kind, Simon

AU - Reiswich, Viktor

AU - Viehweger, Florian

AU - Kluth, Martina

AU - Hube-Magg, Claudia

AU - Bernreuther, Christian

AU - Büscheck, Franziska

AU - Putri, Devita

AU - Clauditz, Till S

AU - Fraune, Christoph

AU - Hinsch, Andrea

AU - Jacobsen, Frank

AU - Krech, Till

AU - Lebock, Patrick

AU - Steurer, Stefan

AU - Burandt, Eike

AU - Minner, Sarah

AU - Marx, Andreas H

AU - Simon, Ronald

AU - Sauter, Guido

AU - Menz, Anne

N1 - This article is protected by copyright. All rights reserved.

PY - 2023/2

Y1 - 2023/2

N2 - Cytokeratin 13 (CK13) is a type I acidic low molecular weight cytokeratin, which is mainly expressed in urothelium and in the squamous epithelium of various sites of origin. Loss of CK13 has been implicated in the development and progression of squamous epithelial neoplasms. To comprehensively determine CK13 expression in normal and neoplastic tissues, a tissue microarray containing 10,439 samples from 131 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. CK13 immunostaining was detectable in 42 (32.1%) of the 131 tumor categories including 24 (18.3%) tumor types with at least one strongly positive case. The highest rate of positive staining was found in various urothelial neoplasms (52.1-92.3%) including Brenner tumor of the ovary (86.8%) and in squamous cell carcinomas from various sites of origin (39.1-77.6%), Warthin tumors of parotid glands (66.7%), adenosquamous carcinomas of the cervix (33.3%), thymomas (16.0%), and endometroid carcinomas of the ovary (15.3%). Twenty other epithelial or germ cell neoplasms showed - a usually weak - CK13 positivity in less than 15% of the cases. In bladder cancer, reduced CK13 expression was linked to high grade and advanced stage (p < 0.0001 each). In squamous cell carcinoma of the cervix, reduced CK13 immunostaining was related to high grade (p = 0.0295) and shortened recurrence-free (p = 0.0094) and overall survival (p = 0.0274). In a combined analysis of 1,151 squamous cell carcinomas from 11 different sites of origin, reduced CK13 staining was linked to high grade (p = 0.0050). Our data provide a comprehensive overview on CK13 expression in normal and neoplastic human tissues. CK13 expression predominates in urothelial neoplasms and in squamous cell carcinomas of different organs, and a loss of CK13 expression is associated with aggressive disease in these tumors.

AB - Cytokeratin 13 (CK13) is a type I acidic low molecular weight cytokeratin, which is mainly expressed in urothelium and in the squamous epithelium of various sites of origin. Loss of CK13 has been implicated in the development and progression of squamous epithelial neoplasms. To comprehensively determine CK13 expression in normal and neoplastic tissues, a tissue microarray containing 10,439 samples from 131 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. CK13 immunostaining was detectable in 42 (32.1%) of the 131 tumor categories including 24 (18.3%) tumor types with at least one strongly positive case. The highest rate of positive staining was found in various urothelial neoplasms (52.1-92.3%) including Brenner tumor of the ovary (86.8%) and in squamous cell carcinomas from various sites of origin (39.1-77.6%), Warthin tumors of parotid glands (66.7%), adenosquamous carcinomas of the cervix (33.3%), thymomas (16.0%), and endometroid carcinomas of the ovary (15.3%). Twenty other epithelial or germ cell neoplasms showed - a usually weak - CK13 positivity in less than 15% of the cases. In bladder cancer, reduced CK13 expression was linked to high grade and advanced stage (p < 0.0001 each). In squamous cell carcinoma of the cervix, reduced CK13 immunostaining was related to high grade (p = 0.0295) and shortened recurrence-free (p = 0.0094) and overall survival (p = 0.0274). In a combined analysis of 1,151 squamous cell carcinomas from 11 different sites of origin, reduced CK13 staining was linked to high grade (p = 0.0050). Our data provide a comprehensive overview on CK13 expression in normal and neoplastic human tissues. CK13 expression predominates in urothelial neoplasms and in squamous cell carcinomas of different organs, and a loss of CK13 expression is associated with aggressive disease in these tumors.

U2 - 10.1111/apm.13280

DO - 10.1111/apm.13280

M3 - SCORING: Journal article

C2 - 36269681

VL - 131

SP - 77

EP - 91

JO - APMIS

JF - APMIS

SN - 0903-4641

IS - 2

ER -