Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
Flow cytometry assay then determined that TCF over-expression helps HCC cell G1/S phase transition, and further research showed that TCF19 up-regulation inhibits p57Kip2, p21Cip1 and p27Kip1 cell cycle suppressors, enhances the expression of cyclin D1 expression and simulates retinoblastoma (Rb), FOXO1 and AKT phosphorylation.
|
30509085 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Importantly, by large-scale analyses, we identified a cluster of long noncoding RNAs, <i>GBAP1</i>, <i>MCM3AP-AS1</i>, <i>SLC16A1-AS1</i>, <i>C3P1</i>, <i>DIO3OS</i>, and <i>HNF4A-AS1</i> as candidate biomarkers for the diagnosis and prognosis of hepatocellular carcinoma, which will improve our understanding of competitive endogenous RNA-mediated regulatory mechanisms underlying hepatocellular carcinoma development and will provide novel therapeutic targets in the future.
|
31761783 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
These data demonstrate that HNF4α does not play a major role during β-catenin-driven HCC, thus revealing that the tumour suppressor role of HNF4α is far more complex and dependent probably on its temporal expression and tumour context.
|
30721564 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Using an inducible knockout model of the tumor-suppressive isoform of hepatocyte nuclear factor 4 alpha ("P1-HNF4α") in the liver in combination with prolonged high fat (HF) diet, we found that HCC developed equally in male and female mice as early as 38 weeks of age.
|
31575546 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Here, we report that the combination of hepatocyte nuclear factor 1A (HNF1A), HNF4A and forkhead box protein A3 (FOXA3) synergistically reprograms hepatocellular carcinoma (HCC) cells to hepatocyte-like cells (reprogrammed hepatocytes, rHeps).
|
30560924 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Liver cancer dedifferentiation markers (AFP, CD133, EPCAM, and KRT19) were found to be progressively increased while hepatocyte terminal differentiation markers (ALB, G6PC, CYP3A4, and HNF4A) were progressively decreased from HCC patients with low SOX signature scores to patients with high SOX signature scores.
|
31462277 |
2019 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
Dysregulation of HNF4α expression has been associated with many human diseases such as ulcerative colitis, colon cancer, maturity-onset diabetes of the young, liver cirrhosis, and hepatocellular carcinoma.
|
31435165 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Here we report that the human FBP1 gene is regulated by two liver-enriched transcription factors, CCAAT-enhancer binding protein-α (C/EBPα) and hepatocyte nuclear factor 4α (HNF4α) in human hepatoma HepG2 cells.
|
29566023 |
2018 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
These data suggest that manipulation of the circadian clock in HNF4α-positive HCC could be a tractable strategy to inhibit tumor growth and progression in the liver.
|
30341289 |
2018 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Several key molecules, such as hsa-miR-195, lncRNA MALAT1 and TFs TAF1 and HNF4α, may contribute to the progression of HCC.
|
30249878 |
2018 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
However, our present data demonstrated that single transduction of HNF4A or HNF1A had only a limited effect on suppression of HCC cell proliferation.
|
30220099 |
2018 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
Gadoxetic acid-enhanced magnetic resonance imaging reflects co-activation of β-catenin and hepatocyte nuclear factor 4α in hepatocellular carcinoma.
|
28488786 |
2018 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
circRNA_104075 stimulates YAP-dependent tumorigenesis through the regulation of HNF4a and may serve as a diagnostic marker in hepatocellular carcinoma.
|
30361504 |
2018 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
Moreover, we also found that miR-194/192 binds the 3'-UTR of these mRNAs. siRNA knockdown of HNF4α suppressed miR-194/192 expression in human hepatocellular carcinoma (HCC) cells and resulted in up-regulation of their mRNA targets.
|
28465351 |
2017 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
High P2-HNF4α expression was significantly associated with poor differentiation of HCC (<i>p</i> = 0.002) and vascular invasion (<i>p</i> = 0.017).
|
29051787 |
2017 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
This work suggested that OA increased PKM1/PKM2 ratio, resulting in HNF-4α activation and hepatoma differentiation.
|
28726775 |
2017 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Together, our results identify Exo70 as a novel transcriptional target of HNF4α to promote cell cycle progression in hepatoma, thus provide a basis for the development of therapeutic strategies for hepatocellular carcinoma.
|
26848864 |
2016 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
However, the role of HNF4α in Hepatitis C Virus (HCV)-related hepatocarcinoma has not been evaluated and remains controversial.
|
27477312 |
2016 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Multiple sets of genes and molecular biological processes involved during HCC development were identified from this integrative analysis: (i) Loss of liver cellular features due to the reduced HNF4A & PPAR signaling in the early stages of HCC, (ii) activated inflammatory and stress signals in the cirrhosis stages and (iii) highly activated cellular proliferation with the activated E2F-MYC oncogenic signaling with the gain of embryonic liver stem cell-like features in the advanced stage tumors.
|
27194100 |
2016 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
ASK1 expression was dramatically suppressed and correlated with HNF4α levels in HCC tissues.
|
27050273 |
2016 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Conditioned medium collected from in vitro MSC-HNF4α cultures significantly inhibited hepatoma cell growth and metastasis compared with controls.
|
27124543 |
2016 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
In summary, our results reveal a novel Hnf4α/miR-122/GALNT10 regulatory pathway that facilitates EGF miR-122 activation and hepatoma growth in HBV-associated hepatocarcinogenesis.
|
25422324 |
2015 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
However, we discovered that these discrete 351 transcripts and 304 proteins screened share extrusive significant-pathways/networks with a 77% overlap, including active TGF-β, RAS, NFκB, and Wnt, and inactive HNF4A, which are responsible for HCC metastasis.
|
25652264 |
2015 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Our findings show that: (I) HNF4 is a common potential transcription factor mediating the transcription of NAFLD progression genes (II) mice HCC derived from NAFLD co-cluster with a less aggressive human HCC subtype of differential prognosis and mixed etiology (III) the HCC survival signature is able to correctly classify 95% of the samples and gives Fgf20 and Tgfb1i1 as the most robust genes for prediction (IV) the expression values of genes composing the signature in an independent human HCC dataset revealed different HCC subtypes showing differences in survival time by a Logrank test.
|
25993042 |
2015 |
Liver carcinoma
|
0.300 |
AlteredExpression
|
disease |
BEFREE |
Ectopic overexpression of HBx in HepG2 cells inhibits HNF-4α expression, and HNF-4α levels were inversely correlated with viral proteins both in HBV-infected HepG2215 cells and as well as HBV positive HCC liver tissues.
|
25238230 |
2014 |