Desmoglein 3 (Dsg3) expression in cancer: A tissue microarray study on 15,869 tumors.


Journal

Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 16 08 2022
revised: 03 11 2022
accepted: 04 11 2022
pubmed: 15 11 2022
medline: 7 12 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

Desmoglein-3 (Dsg3) is a transmembrane glycoprotein which is preferably found in desmosomes of keratinocytes in squamous epithelium. Both loss and upregulation of Dsg3 have been implicated in cancer progression. To comprehensively evaluate Dsg3 expression in normal and neoplastic tissues, a tissue microarray containing 15,869 samples from 137 different tumor types and subtypes as well as 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. Dsg3 immunostaining was detectable in 47 (34.3 %) tumor categories including 15 (10.9 %) tumor types with at least one strongly positive case. The highest rate of Dsg3 positivity was found in squamous cell carcinomas from various sites (71.2-97.3 %), basal cell carcinomas of the skin (41.9 %), various tumors from salivary glands (12.9-38.9 %), and in urothelial neoplasms (2.1-20.7 %). Dsg3 positivity in less than 10 % of cases was seen in 23 additional cancer categories. Dsg3 staining was almost always weak and rarely moderate in these tumors. High Dsg3 expression was linked to invasive growth in urothelial carcinoma (p < 0.0001), as well as to advanced pT stage (p = 0.0102), nodal metastasis (p = 0.0162), blood vessel infiltration (p = 0.0189) and lymph vessel infiltration (p = 0.0151) in colorectal cancer. Reduced Dsg3 expression was linked to high grade in a cohort of 599 squamous cell carcinomas from 11 different sites of origin (p < 0.0001). Associations between Dsg3 immunostaining and clinicopathological features were not found in invasive breast cancer of no special type, ductal adenocarcinomas of the pancreas and in gastric adenocarcinomas. In summary, Dsg3 expression predominates in squamous cell carcinomas and loss of Dsg3 immunostaining goes along with dedifferentiation of these tumors. The identification of focal squamous differentiation in other neoplasms may constitute a diagnostic application of Dsg3 immunohistochemistry.

Identifiants

pubmed: 36375372
pii: S0344-0338(22)00444-7
doi: 10.1016/j.prp.2022.154200
pii:
doi:

Substances chimiques

Desmoglein 3 0
DSG3 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

154200

Informations de copyright

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

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The Dsg3 antibody clone MSVA-543M was provided from MS Validated Antibodies GmbH (owned by a family member of GS). Conflict of interests The Dsg3 antibody clone MSVA-543M was provided from MS Validated Antibodies GmbH (owned by a family member of GS).

Auteurs

Florian Viehweger (F)

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

Ahmad Azem (A)

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

Natalia Gorbokon (N)

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

Ria Uhlig (R)

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.

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.

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 H Marx (AH)

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.

Andrea Hinsch (A)

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

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Classifications MeSH