Cytokeratin 10 (CK10) expression in cancer: A tissue microarray study on 11,021 tumors.


Journal

Annals of diagnostic pathology
ISSN: 1532-8198
Titre abrégé: Ann Diagn Pathol
Pays: United States
ID NLM: 9800503

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 17 08 2022
accepted: 18 08 2022
pubmed: 28 8 2022
medline: 19 10 2022
entrez: 27 8 2022
Statut: ppublish

Résumé

Cytokeratin 10 (CK10) is a type I acidic low molecular weight cytokeratin which is mainly expressed in keratinizing squamous epithelium of the skin. Variable levels of CK10 protein have been described in squamous carcinomas of different sites and in some other epithelial neoplasms. To comprehensively determine the prevalence of CK10 expression in normal and neoplastic tissues, a tissue microarray containing 11,021 samples from 131 different tumor types and subtypes was analyzed by immunohistochemistry. CK10 immunostaining was detectable in 41 (31.3 %) of 131 tumor categories, including 18 (13.7 %) tumor types with at least one strongly positive case. The highest rate of positive staining was found in squamous cell carcinomas from various sites of origin (positive in 18.6 %-66.1 %) and in Warthin tumors of salivary glands (47.8 %), followed by various tumor entities known to potentially exhibit areas with squamous cell differentiation such as teratomas (33.3 %), basal cell carcinomas of the skin (14.3 %), adenosquamous carcinomas of the cervix (11.1 %), and several categories of urothelial neoplasms (3.1 %-16.8 %). In a combined analysis of 956 squamous cell carcinomas from 11 different sites of origin, reduced CK10 staining was linked to high grade (p < 0.0001) and advanced stage (p = 0.0015) but unrelated to HPV infection. However, CK10 staining was not statistically related to grade (p = 0.1509) and recurrence-free (p = 0.5247) or overall survival (p = 0.5082) in 176 cervical squamous cell carcinomas. In the urinary bladder, CK10 staining occurred more commonly in muscle-invasive (17.7 %) than in non-invasive urothelial carcinomas (4.0 %-6.0 %; p < 0.0001). In summary, our data corroborate a role of CK10 as a suitable marker for mature, keratinizing squamous cell differentiation in epithelial tissues. CK10 immunohistochemistry may thus be instrumental for a more objective evaluation of the clinical significance of focal squamous differentiation in cancer.

Identifiants

pubmed: 36029589
pii: S1092-9134(22)00131-9
doi: 10.1016/j.anndiagpath.2022.152029
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Keratins 68238-35-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152029

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The monoclonal mouse CK10 antibody, clone MSVA-610M was provided from MS Validated Antibodies GmbH (owned by a family member of GS).

Auteurs

Ria Uhlig (R)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Moussa Abboud (M)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Natalia Gorbokon (N)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Maximilian Lennartz (M)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Sebastian Dwertmann Rico (S)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Simon Kind (S)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Viktor Reiswich (V)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Florian Viehweger (F)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Martina Kluth (M)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Claudia Hube-Magg (C)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Christian Bernreuther (C)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Franziska Büscheck (F)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Till S Clauditz (TS)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Christoph Fraune (C)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Andrea Hinsch (A)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Frank Jacobsen (F)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Till Krech (T)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Institute of Pathology, Clinical Center Osnabrueck, Osnabrueck, Germany.

Patrick Lebok (P)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Institute of Pathology, Clinical Center Osnabrueck, Osnabrueck, Germany.

Stefan Steurer (S)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Eike Burandt (E)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Sarah Minner (S)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Andreas Marx (A)

Department of Pathology, Academic Hospital Fuerth, Fuerth, Germany.

Ronald Simon (R)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: R.Simon@uke.de.

Guido Sauter (G)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Anne Menz (A)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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