Article

The correlations between the expression of FGFR4 protein and clinicopathological parameters as well as prognosis of gastric cancer patients.

Department of Gastrointestinal Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou, Henan Province, China. .
Journal of Surgical Oncology (impact factor: 2.1). 05/2012; DOI:10.1002/jso.23153
Source: PubMed

ABSTRACT BACKGROUND: Fibroblast growth factor receptor 4 (FGFR4) was seldom investigated in gastric cancer (GC). The purpose of the study was to elucidate the expression of FGFR4 protein in GC and related clinical significance. METHODS: Ninety-four paraffin-embedded tumor specimens were obtained from Cancer Hospital, Fudan University. The expression of FGFR4 as well as p53, p21, EGFR, neu, c-myc, and PCNA were detected by immunohistochemical method. Then, correlation analysis and survival analysis were performed. RESULTS: The expression rate of FGFR4 protein in GC tissues and normal stomach tissues was 93.6% and 30.8%, respectively (P = 0.000). The expression of FGFR4 was positively correlated with the expression of p21, neu and PCNA (P-value was 0.009, 0.012, and 0.018, respectively). Subgroup analysis showed that compared to low expression group, the prognosis of patients with III/IV stage and negative expression of p21 in high expression group of FGFR4 were worse (P = 0.048, 0.041, respectively). Multivariate analysis showed that TNM stage was the independent prognostic factor in high expression group (HR, 11.593; 95% CI, 3.532-18.058; P = 0.000). CONCLUSIONS: High expression of FGFR4 protein, accelerating the progression of advanced GC, might be associated with a poor prognosis in patients with advanced FC. J. Surg. Oncol © 2012 Wiley Periodicals, Inc.

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Keywords

Cancer Hospital
 
clinical significance
 
correlation analysis
 
expression rate
 
FGFR4
 
FGFR4 protein
 
Fibroblast growth factor receptor 4
 
gastric cancer
 
GC tissues
 
independent prognostic factor
 
J. Surg
 
low expression group
 
Multivariate analysis
 
negative expression
 
normal stomach tissues
 
Oncol © 2012 Wiley Periodicals
 
paraffin-embedded tumor specimens
 
poor prognosis
 
Subgroup analysis
 
survival analysis