Published December 2013 | Version v1
Journal article

High RAB25 expression is associated with good clinical outcome in patients with locally advanced head and neck squamous cell carcinoma

  • 1. Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Barcelona (Spain)
  • 2. Grup d'Oncogènesi i Antitumorals (GOA), Institut d'Investigacions Biomèdiques Sant Pau (IIB-Sant Pau), Barcelona (Spain)
  • 3. Department of Otorhinolaryngology (ORL), Hospital de la Santa Creu i Sant Pau, Barcelona (Spain)
  • 4. Department of Pathology, Clínica Girona, Girona (Spain)
  • 5. Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona (Spain)
  • 6. Department of Pharmacy, IIB-Sant Pau, Hospital de la Santa Creu i Sant Pau, Barcelona (Spain)

Description

Currently there are no molecular markers able to predict clinical outcome in locally advanced head and neck squamous cell carcinoma (HNSCC). In a previous microarray study, RAB25 was identified as a potential prognostic marker. The aim of this study was to analyze the association between RAB25 expression and clinical outcome in patients with locally advanced HNSCC treated with standard therapy. In a retrospective immunohistochemical study (n = 97), we observed that RAB25-negative tumors had lower survival (log-rank, P = 0.01) than patients bearing positive tumors. In an independent prospective mRNA study (n = 117), low RAB25 mRNA expression was associated with poor prognosis. Using classification and regression tree analysis (CART) we established two groups of patients according to their RAB25 mRNA level and their risk of death. Low mRNA level was associated with poor local recurrence-free (log-rank, P = 0.005), progression-free (log-rank, P = 0.002) and cancer-specific (log-rank, P < 0.001) survival. Multivariate Cox model analysis showed that low expression of RAB25 was an independent poor prognostic factor for survival (hazard ratio: 3.84, 95% confidence interval: 1.93–7.62, P < 0.001). Patients whose tumors showed high RAB25 expression had a low probability of death after treatment. We also found lower RAB25 expression in tumors than in normal tissue (Mann–Whitney U, P < 0.001). Moreover, overexpression of RAB25 in the UM-SCC-74B HNSCC cell line increased cisplatin sensitivity, and reduced cell migration and invasion. Our findings support a tumor suppressor role for RAB25 in HNSCC and its potential use to identify locally advanced patients with a high probability of survival after genotoxic treatment

Availability note (English)

Available from http://dx.doi.org/10.1002/cam4.153; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892400

Additional details

Publishing Information

Journal Title
Cancer medicine
Journal Volume
2
Journal Issue
6
Journal Page Range
p. 950-963
ISSN
2045-7634

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46049608
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CARCINOMAS; CLASSIFICATION; DEATH; HAZARDS; HEAD; MIGRATION; NECK; PATIENTS; SENSITIVITY; THERAPY
Descriptors DEC
BODY; DISEASES; MEDICINE; NEOPLASMS

Optional Information

Copyright
Copyright (c) 2013 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.
Notes
PMCID: PMC3892400; PMID: 24403269; OAI: oai:pubmedcentral.nih.gov:3892400; Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.