Article

Expression of major vault protein gene in osteosarcoma patients.

Department of Pediatrics, Instituto de Oncologia Pediátrica, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, Brazil, and Applied Molecular Oncology, Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada.
Journal of Orthopaedic Research (impact factor: 2.81). 07/2007; 25(7):958-63. DOI:10.1002/jor.20371 pp.958-63
Source: PubMed

ABSTRACT Osteosarcoma (OS) is a primary malignant tumor of bone. Despite the successful use of multiple chemotherapeutic agents in the treatment of OS, more than 30% of OS tumors remain resistant to treatment. Elucidation of cellular resistance mechanisms may lead to better treatments for cancer patients. In this study, we used the low-density expression cDNA array, GEArray Q Series Human Cancer Drug Resistance and Metabolism Gene Array to screen genes related to drug resistance in 15 OS tumors. Expression patterns of the MPV gene were validated by real time PCR on 45 OS patient tumor samples and correlated with clinical and pathological data. Major vault protein (MVP) expression was present in 24 (53%) tumor samples and absent in 21 (47%). Samples from surgery showed correlation between the expression of MVP, metastatic disease at diagnosis and event free survival (EFS). The MVP gene expression correlates with metastatic disease at diagnosis after neoadjuvant chemotherapy (p=0.048), and is also associated with worse EFS (p=0.036). These findings suggest that MVP expression is involved in one of the mechanisms of drug resistance in OS and is induced by chemotherapy.

0 0
 · 
0 Bookmarks
 · 
37 Views

Keywords

15 OS tumors
 
45 OS patient tumor samples
 
cancer patients
 
cellular resistance mechanisms
 
event free survival
 
Expression patterns
 
GEArray Q Series Human Cancer Drug Resistance
 
low-density expression cDNA array
 
Major vault protein
 
Metabolism Gene Array
 
MPV gene
 
MVP expression
 
MVP gene expression correlates
 
neoadjuvant chemotherapy
 
OS tumors
 
pathological data
 
primary malignant tumor
 
resistant
 
screen genes
 
successful use