Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We showed that FGFR4 expression is markedly increased in high-grade PanIN and PDAC compared with that in normal and low-grade PanIN, and that FGFR4 stimulation by FGF19 of PDAC cells contributes to tumor suppression by increasing cell adhesion to extracellular matrix.
|
21109934 |
2011 |
Carcinogenesis
|
0.040 |
AlteredExpression
|
phenotype |
BEFREE |
The changes in mRNA levels associated with transformation and tumorigenesis as a result of FGF19 administration were also evaluated.
|
21109934 |
2011 |
Pancreatic intraepithelial neoplasia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We showed that FGFR4 expression is markedly increased in high-grade PanIN and PDAC compared with that in normal and low-grade PanIN, and that FGFR4 stimulation by FGF19 of PDAC cells contributes to tumor suppression by increasing cell adhesion to extracellular matrix.
|
21109934 |
2011 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
0.010 |
Biomarker
|
disease |
BEFREE |
We showed that FGFR4 expression is markedly increased in high-grade PanIN and PDAC compared with that in normal and low-grade PanIN, and that FGFR4 stimulation by FGF19 of PDAC cells contributes to tumor suppression by increasing cell adhesion to extracellular matrix.
|
21109934 |
2011 |
Diabetes Mellitus
|
0.060 |
Biomarker
|
group |
BEFREE |
Mutations in Klotho/beta-Klotho or fgf19, -21, or -23 are associated with a number of human diseases, including autosomal dominant hypophosphatemic rickets, premature aging disorders, and diabetes.
|
21177529 |
2011 |
Diabetes
|
0.050 |
Biomarker
|
disease |
BEFREE |
Mutations in Klotho/beta-Klotho or fgf19, -21, or -23 are associated with a number of human diseases, including autosomal dominant hypophosphatemic rickets, premature aging disorders, and diabetes.
|
21177529 |
2011 |
Diarrhoea predominant irritable bowel syndrome
|
0.020 |
Biomarker
|
disease |
BEFREE |
The FGF19-FGFR4-KLB pathway links regulation of BA synthesis to colonic transit in IBS-D.
|
21396369 |
2011 |
Liver carcinoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Although it is widely assumed that CCND1 is the main driving oncogene of this common amplicon (15% frequency in HCC), both forward-transformation assays and RNAi-mediated inhibition in human HCC cells established that FGF19 is an equally important driver gene in HCC.
|
21397858 |
2011 |
Malignant neoplasm of liver
|
0.020 |
Biomarker
|
disease |
BEFREE |
Identification of a therapeutic strategy targeting amplified FGF19 in liver cancer by Oncogenomic screening.
|
21397858 |
2011 |
Adult Liver Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Identification of a therapeutic strategy targeting amplified FGF19 in liver cancer by Oncogenomic screening.
|
21397858 |
2011 |
Liver and Intrahepatic Biliary Tract Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Identification of a therapeutic strategy targeting amplified FGF19 in liver cancer by Oncogenomic screening.
|
21397858 |
2011 |
Non-alcoholic Fatty Liver Disease
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Soluble FGFR4 extracellular domain inhibits FGF19-induced activation of FGFR4 signaling and prevents nonalcoholic fatty liver disease.
|
21616061 |
2011 |
Steatohepatitis
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
FGFR4-ECD inhibited FGF19-induced activation of FGFR4 signaling and reduced steatosis of HepG2 induced by palmitic acid in vitro.
|
21616061 |
2011 |
Liver carcinoma
|
0.400 |
Biomarker
|
disease |
BEFREE |
Moreover, we found that the FGF19 recombinant protein could increase the proliferation (P < 0.01, n = 12) and invasion (P < 0.01, n = 6) capabilities of human hepatocellular carcinoma cell lines and inhibited their apoptosis (P < 0.01, n = 12).
|
22309595 |
2012 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Univariate and multivariate analyses revealed that the tumor FGF19 mRNA expression was an independent prognostic factor for overall and disease-free survival.
|
22309595 |
2012 |
Hepatocarcinogenesis
|
0.080 |
Biomarker
|
disease |
BEFREE |
Although fibroblast growth factor 19 (FGF19) can promote liver carcinogenesis in mice, its involvement in human hepatocellular carcinoma (HCC) has not been well investigated.
|
22309595 |
2012 |
Tumor Cell Invasion
|
0.070 |
Biomarker
|
phenotype |
BEFREE |
Moreover, we found that the FGF19 recombinant protein could increase the proliferation (P < 0.01, n = 12) and invasion (P < 0.01, n = 6) capabilities of human hepatocellular carcinoma cell lines and inhibited their apoptosis (P < 0.01, n = 12).
|
22309595 |
2012 |
Tumor Progression
|
0.050 |
Biomarker
|
phenotype |
BEFREE |
To test the role of the FGF19/FGFR4 system in tumor progression, we used recombinant FGF19 protein and small interfering RNA (siRNA) of FGF19 and FGFR4 to regulate their concentrations.
|
22309595 |
2012 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
Recent studies suggest that betaKlotho (KLB) and endocrine FGF19 and FGF21 redirect FGFR signaling to regulation of metabolic homeostasis and suppression of obesity and diabetes.
|
22442730 |
2012 |
Diabetes Mellitus
|
0.060 |
Biomarker
|
group |
BEFREE |
Recent studies suggest that betaKlotho (KLB) and endocrine FGF19 and FGF21 redirect FGFR signaling to regulation of metabolic homeostasis and suppression of obesity and diabetes.
|
22442730 |
2012 |
Diabetes
|
0.050 |
Biomarker
|
disease |
BEFREE |
Recent studies suggest that betaKlotho (KLB) and endocrine FGF19 and FGF21 redirect FGFR signaling to regulation of metabolic homeostasis and suppression of obesity and diabetes.
|
22442730 |
2012 |
Squamous cell carcinoma of esophagus
|
0.010 |
Biomarker
|
disease |
BEFREE |
Novel oncogenes identified within the 11q13 amplicon including FGF19 and SHANK2 may play important roles in ESCC tumorigenesis.
|
22761904 |
2012 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The miR-34a/βKL/FGF19 axis may present unique therapeutic targets for FGF19-related human diseases, including metabolic disorders and cancer.
|
22988100 |
2012 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
Aberrantly elevated microRNA-34a in obesity attenuates hepatic responses to FGF19 by targeting a membrane coreceptor β-Klotho.
|
22988100 |
2012 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
The miR-34a/βKL/FGF19 axis may present unique therapeutic targets for FGF19-related human diseases, including metabolic disorders and cancer.
|
22988100 |
2012 |