Large-scale human tissue analysis identifies Uroplakin 1a as a putative diagnostic marker for urothelial cancer.


Journal

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

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 31 03 2022
revised: 12 07 2022
accepted: 16 07 2022
pubmed: 26 7 2022
medline: 26 10 2022
entrez: 25 7 2022
Statut: ppublish

Résumé

Uroplakin 1A (Upk1a) protein is relevant for stabilizing and strengthening urothelial cells and helps to prevent them from rupturing during bladder distension. Based on RNA expression data Upk1a is expressed in a limited number of normal tissues and tumors. To comprehensively evaluate the potential diagnostic and prognostic utility of Upk1a immunohistochemistry, a tissue microarray containing 6929 samples from 115 different tumor types and subtypes and 608 samples of 76 different normal tissue types was analyzed. Upk1a positivity was found in 34 (29.6 %) different tumor types including 9 (7.8 %) tumor types with at least one strongly positive case. The highest rates of Upk1a positivity were seen in various subtypes of urothelial neoplasms (42.6-98 %) including Brenner tumors of the ovary (64.9 %) followed by neoplasms of the thyroid (10.4-33.3 %). In urothelial tumors, Upk1a staining predominated at the cell membranes and staining intensity was often moderate to strong. In thyroidal neoplasms the staining was mostly purely cytoplasmic and of low to moderate intensity. Upk1a positivity was also seen in up to 15 % of cases in 25 additional tumor categories but the staining intensity was often cytoplasmic and the intensity was usually judged as weak and only rarely as moderate. Within non-invasive (pTa) tumors, the Upk1a positivity rate decreased from 94 % in pTa G2 (low grade) to 90.1 % in pTa G3 (p = 0.012) and was even lower in muscle-invasive carcinomas (41.5 %; p < 0.0001 vs pTaG3). Within muscle invasive carcinomas, Upk1a expression was unrelated to nodal metastasis (p > 0.05) and patient outcome (p > 0.05). In conclusion, Upk1a immunohistochemistry is a potentially useful and specific diagnostic marker for the distinction of urothelial carcinomas from other neoplasms. However, its sensitivity is less than 50 % in muscle-invasive cancers because Upk1a expression decreases during grade and stage progression.

Identifiants

pubmed: 35872365
pii: S0344-0338(22)00272-2
doi: 10.1016/j.prp.2022.154028
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
RNA 63231-63-0
Uroplakin Ia 0
UPK1A protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

154028

Informations de copyright

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

Déclaration de conflit d'intérêts

Declaration of Competing Interest The Uroplakin 1A antibody clone MSVA-735M was provided from MS Validated Antibodies GmbH (owned by a family member of GS).

Auteurs

Viktor Reiswich (V)

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

Steffi Könemann (S)

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

Maximilian Lennartz (M)

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

Doris Höflmayer (D)

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

Anne Menz (A)

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

Viktoria Chirico (V)

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

Claudia Hube-Magg (C)

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

Christoph Fraune (C)

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

Christian Bernreuther (C)

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

Ronald Simon (R)

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

Till S Clauditz (TS)

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

Guido Sauter (G)

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

Andrea Hinsch (A)

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

Simon Kind (S)

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

Frank Jacobsen (F)

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

Stefan Steurer (S)

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

Sarah Minner (S)

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

Franziska Büscheck (F)

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

Eike Burandt (E)

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

Andreas H Marx (AH)

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Pathology, Academic Hospital Fuerth, Fuerth, Germany.

Patrick Lebok (P)

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

Till Krech (T)

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

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH