کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2776017 | 1152357 | 2007 | 5 صفحه PDF | دانلود رایگان |
BackgroundThe increased expression of the fibroblast growth factor receptor 4 (FGFR4) has been identified in many human cancers. Recently, a single nucleotide polymorphism changing the sense codon 388 from glycine to arginine was identified in the FGFR4 gene. The FGFR4 Arg388 allele was found to be associated with a poor prognosis for positive node breast cancer, high-grade soft-tissue sarcoma, colon carcinoma, and head and neck squamous cell carcinoma (HNSCC).MethodsWe decided to verify the impact of the FGFR4 Arg388 allele on survival as well as its association with histoclinical data in 75 cases of HNSCC. The FGFR4 Arg388 allele was detected by PCR-RFLP and DNA sequencing.ResultsThe FGFR4 Arg388 allele was detected in 42.5% of the tumors (37% heterozygous Gly/Arg and 5.5% homozygous Arg/Arg). The presence of at least one Arg allele was significantly correlated with reduced overall survival after 24 months of follow-up. The cases involving the Arg allele presented an increased mortality risk of 2.2 if compared to the non-carrier cases.ConclusionThe FGFR4 Arg388 allele is associated with a shortened survival.
Journal: Experimental and Molecular Pathology - Volume 82, Issue 1, February 2007, Pages 53–57