[Urachal Cancer: an update of current molecular findings].

Das Urachuskarzinom: Ein Update aktueller molekularer Ergebnisse.

Journal

Der Pathologe
ISSN: 1432-1963
Titre abrégé: Pathologe
Pays: Germany
ID NLM: 8006541

Informations de publication

Date de publication:
Dec 2019
Historique:
pubmed: 11 11 2019
medline: 11 1 2020
entrez: 10 11 2019
Statut: ppublish

Résumé

Urachal cancer is a rare type of cancer, often following a clinically aggressive course. Due to its rarity, knowledge about its molecular background is still limited. In addition, no sufficiently reliable diagnostic markers are available. The aim of the present study is to give an overview of our recent molecular projects on urachal cancer and to connect it with current literature in the field. Three projects are introduced. The first project identified and validated diagnostic biomarkers in urachal adenocarcinomas compared to colorectal adenocarcinomas and primary adenocarcinomas of the bladder using various proteomic methods. In the second project, the most relevant differential diagnostic markers between urachal adenocarcinomas and colorectal adenocarcinomas compared to normal tissue (urachal remnants) were determined by analyzing a miRNA panel. Sequence analyses were performed in the third project. The focus was on molecular differences to colorectal adenocarcinomas and urothelial carcinomas. We detected potential biomarker candidates for the immunohistochemical differential-diagnosis and generated a miRNA-based diagnostic scoring system with a potentially high differential-diagnostic significance. The sequence analyses data confirm the molecular autonomy of the urachal adenocarcinomas compared to other entities.

Sections du résumé

BACKGROUND BACKGROUND
Urachal cancer is a rare type of cancer, often following a clinically aggressive course. Due to its rarity, knowledge about its molecular background is still limited. In addition, no sufficiently reliable diagnostic markers are available.
OBJECTIVES OBJECTIVE
The aim of the present study is to give an overview of our recent molecular projects on urachal cancer and to connect it with current literature in the field.
MATERIALS AND METHODS METHODS
Three projects are introduced. The first project identified and validated diagnostic biomarkers in urachal adenocarcinomas compared to colorectal adenocarcinomas and primary adenocarcinomas of the bladder using various proteomic methods. In the second project, the most relevant differential diagnostic markers between urachal adenocarcinomas and colorectal adenocarcinomas compared to normal tissue (urachal remnants) were determined by analyzing a miRNA panel. Sequence analyses were performed in the third project. The focus was on molecular differences to colorectal adenocarcinomas and urothelial carcinomas.
RESULTS AND CONCLUSIONS CONCLUSIONS
We detected potential biomarker candidates for the immunohistochemical differential-diagnosis and generated a miRNA-based diagnostic scoring system with a potentially high differential-diagnostic significance. The sequence analyses data confirm the molecular autonomy of the urachal adenocarcinomas compared to other entities.

Identifiants

pubmed: 31705235
doi: 10.1007/s00292-019-00689-4
pii: 10.1007/s00292-019-00689-4
doi:

Substances chimiques

Genetic Markers 0

Types de publication

Journal Article

Langues

ger

Sous-ensembles de citation

IM

Pagination

239-243

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Auteurs

H Reis (H)

Institut für Pathologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland. henning.reis@uk-essen.de.

F Mairinger (F)

Institut für Pathologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland.

S Ting (S)

Institut für Pathologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland.

N Nagy (N)

Klinik für Urologie, Semmelweis Universität, Budapest, Ungarn.

K E Witzke (KE)

Medizinisches Proteom Center, Ruhr-Universität Bochum, Bochum, Deutschland.

M Kohl (M)

Medizinisches Proteom Center, Ruhr-Universität Bochum, Bochum, Deutschland.

B Sitek (B)

Medizinisches Proteom Center, Ruhr-Universität Bochum, Bochum, Deutschland.

C Niedworok (C)

Klinik für Urologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland.

B Hadaschik (B)

Klinik für Urologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland.

P Nyirády (P)

Klinik für Urologie, Semmelweis Universität, Budapest, Ungarn.

T Szarvas (T)

Klinik für Urologie, Semmelweis Universität, Budapest, Ungarn.
Klinik für Urologie, Westdeutsches Tumorzentrum, Universitätsmedizin Essen, Universität Duisburg-Essen, Essen, Deutschland.

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Classifications MeSH