An invited review following the soujinkai young investigator award : Heat shock factor 1 could be a promising new therapeutic target for melanoma
        The bulletin of the Yamaguchi Medical School Volume 63 Issue 1-2
        Page 1-4
        
    published_at 2016
            Title
        
        An invited review following the soujinkai young investigator award : Heat shock factor 1 could be a promising new therapeutic target for melanoma
        
        
    
        
            Source Identifiers
        
                    [PISSN] 0513-1812
                    [NCID] AA00594272
    
    
            Creator Keywords
        
            human melanoma
            heat shock factor 1 (hsf1)
            proliferation
            migration
            invasion
    Heat shock factor 1 (HSF1) has recently been reported to promote malignant transformation and growth. Furthermore, HSF1 was identified as a potent proinvasion oncogene in human melanomas. However, the biological functions of HSF1 in human melanoma remain poorly understood. In this study, we found that silencing HSF1 suppressed proliferation, migration and invasiveness of human melanoma cells in vitro and HSF1 is required for melanoma invasion and metastasis, as well as tumorigenic potential in vivo. Furthermore, we demonstrated that these decreased functions by HSF1 knockdown were restored by overexpression of wild-type HSF1 both in vitro and vivo. Our findings suggest that HSF1 could be a promising new therapeutic target for melanoma.This article is an invited review by the awardee of the Soujinkai Young Investigator Award, based on his original paper published in Cancer Letters in 2014.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        departmental bulletin paper
    
    
        
            Publishers
        
            Yamaguchi University School of Medicine
    
    
        
            Date Issued
        
        2016
    
    
        
            File Version
        
        Version of Record
    
    
        
            Access Rights
        
        open access
    
    
            Relations
        
            
                
                
                [ISSN]0513-1812
            
            
                
                
                [NCID]AA00594272
            
    
