MiRNAs Are Involved in Tall Cell Morphology in Papillary Thyroid Carcinoma.

PTEN TERT VEGF miRNA prognosis tall cell thyroid carcinoma

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
25 Jun 2019
Historique:
received: 17 05 2019
revised: 13 06 2019
accepted: 14 06 2019
entrez: 28 6 2019
pubmed: 28 6 2019
medline: 28 6 2019
Statut: epublish

Résumé

Five percent of papillary thyroid carcinomas (PTC) show an adverse clinical outcome (ACO). The tall cell variant of papillary thyroid carcinomas (TCV) is a good predictor of an ACO, however, the identification of tall-cells is subjective. Micro RNAs are short non-coding ribonucleic acids (miRNA). Their expression in PTC could be a powerful, more objective predictor of prognosis. Forty-four PTC underwent miRNA profiling, twenty-four of them were TCV. The miRNA dataset was validated by analysis of expression of known target proteins (vascular endothelial growth factor (VEGF) and phosphatase and tensin homolog (PTEN)) in 125 patients including 48 TCV and 57 with an ACO. One hundred and forty-nine miRNAs were significantly associated with an ACO, seventy-one of them with TC-morphology. Twenty-two miRNAs were identified as targets for VEGF and thirty-two as targets for PTEN. In univariate and multivariable analysis, reduced expression of PTEN and an increased expression of VEGF were associated with shorter relapse free survival. A classifier, including TC-morphology, pT-stage, VEGF, and PTEN, predicted relapse with an 80% accuracy. Some miRNAs predict outcome in PTC and are involved in TC-morphology in PTC. These miRNAs may serve as more objective indicators of an ACO than tall cell morphology. PTEN and VEGF protein expression are prognostically relevant and are at least partially regulated by miRNAs.

Identifiants

pubmed: 31242620
pii: cancers11060885
doi: 10.3390/cancers11060885
pmc: PMC6628239
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fondation pour la recherche Nuovo-Soldati
ID : NA
Organisme : Research Support Foundation
ID : NA
Organisme : Gertrud Hagmann Stiftung für Malignomforschung
ID : NA
Organisme : Berner Krebsliga
ID : NA

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Auteurs

Laura A Boos (LA)

Institute of Pathology, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. laurie.boos@googlemail.com.

Anja Schmitt (A)

Institute of Pathology, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. anja.schmitt@pathology.unibe.ch.

Holger Moch (H)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Rämistrasse 100, 8091 Zurich, Switzerland. holger.moch@usz.ch.

Paul Komminoth (P)

Institute of Surgical Pathology, Stadtspital Triemli, Birmensdorferstr. 497, 8063 Zürich, Switzerland. Paul.Komminoth@triemli.zuerich.ch.

Cedric Simillion (C)

Department of BioMedical Research, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. cedric.simillion@protonmail.ch.

Ilaria Marinoni (I)

Institute of Pathology, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. ilaria.marinoni@pathology.unibe.ch.

Yuri E Nikiforov (YE)

Department of Pathology and Laboratory Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA. nikiforovye@upmc.edu.

Marina N Nikiforova (MN)

Department of Pathology and Laboratory Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA. nikiforovamn@upmc.edu.

Aurel Perren (A)

Institute of Pathology, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. aurel.perren@pathology.unibe.ch.

Matthias S Dettmer (MS)

Institute of Pathology, University of Bern, Murtenstrasse 31, CH 3008 Bern, Switzerland. matthias.dettmer@pathology.unibe.ch.

Classifications MeSH