Expression of vimentin (VIM) and metastasis-associated 1 (MTA1) protein in laryngeal squamous cell carcinoma are associated with prognostic outcome of patients.
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor
/ genetics
Female
Gene Expression
Humans
Immunohistochemistry
Laryngeal Neoplasms
/ diagnosis
Male
Middle Aged
Prognosis
Receptor, Notch1
/ genetics
Repressor Proteins
/ genetics
Squamous Cell Carcinoma of Head and Neck
/ diagnosis
Survival Rate
Trans-Activators
/ genetics
Vimentin
/ genetics
Head and neck cancer
Laryngeal cancer
Prognostic tumor biomarker
Journal
American journal of otolaryngology
ISSN: 1532-818X
Titre abrégé: Am J Otolaryngol
Pays: United States
ID NLM: 8000029
Informations de publication
Date de publication:
Historique:
received:
23
03
2019
revised:
30
03
2019
accepted:
02
04
2019
pubmed:
14
4
2019
medline:
21
12
2019
entrez:
14
4
2019
Statut:
ppublish
Résumé
Laryngeal squamous cell carcinoma (LSCC), a common type of head and neck cancer, is associated with high rates of metastasis and recurrence. In this study, we investigated the potential combinatorial prognostic value of NOTCH1, Vimentin (VIM), and Metastasis-associated 1 (MTA1) protein in LSCC, using immunohistochemistry. Tissue specimens from 69 patients with LSCC were immunohistochemically evaluated for the protein expression of NOTCH1, VIM, and MTA1. Then, biostatistical analysis was performed, in order to assess the prognostic value of the expression of each one of these proteins. NOTCH1 expression status was not a significant prognosticator in LSCC, as shown in Kaplan-Meier survival analysis. On the contrary, both VIM and MTA1 seem to have an important prognostic potential, independently of TNM staging and histological grade of the tumor. In fact, positive VIM expression was shown to predict patients' relapse and poor outcome regarding patients' overall survival, in contrast with MTA1, the positive expression of which predicts higher disease-free survival (DFS) and overall survival (OS) rates in LSCC. VIM and MTA1 constitute potential tumor biomarkers in LSCC and could be integrated into a multiparametric prognostic model. Undoubtedly, their prognostic value needs further validation in larger cohorts of LSCC patients.
Identifiants
pubmed: 30979652
pii: S0196-0709(19)30256-X
doi: 10.1016/j.amjoto.2019.04.002
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
MTA1 protein, human
0
NOTCH1 protein, human
0
Receptor, Notch1
0
Repressor Proteins
0
Trans-Activators
0
Vimentin
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
487-493Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.