Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
A causal link has been determined between angiotensin II (Ang-II) and HCC.
|
31367864 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
To investigate the effects of angiotensin II (Ang II) and tumor necrosis factor-α (TNF-α) on the biological characteristics of hepatocellular carcinoma (HCC) cells and the associated changes in G protein-coupled receptor kinase 2 (GRK2) expression.
|
30712649 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
This study aimed to investigate the role of angiotensin II and NF-kB pathway in liver hepatocellular carcinoma cell line (HepG2) proliferation by using azilsartan (as a novel Ag II antagonist) and Bay 11-7082 (as NF-kB inhibitor).
|
29710494 |
2018 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Comparative effectiveness of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers in chemoprevention of hepatocellular carcinoma: a nationwide high-risk cohort study.
|
29631561 |
2018 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The objective of this study was to investigate the effect of RAS inhibitor (RASi) treatment (angiotensin-converting enzyme inhibitors or angiotensin-II-receptor blockers) on survival of patients with hepatocellular carcinoma (HCC).
|
29163965 |
2017 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
We recently confirmed that angiotensin II (Ang II) type 1 receptor (AT1R) was overexpressed in hepatocellular carcinoma tissue using a murine hepatoma model.
|
26225830 |
2015 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
The interaction between Angiotensin II (AngII) and angiotensin type 1 receptor (AT1R) may have a pivotal role in hepatocellular carcinoma (HCC) and therefore, AT1R blocker and angiotensin I-converting enzyme (ACE) inhibitors may have therapeutic potential in the treatment of hepatic cancer.
|
24391821 |
2013 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The close relationship between aflatoxins and 249ser TP53 gene mutation (AGG to AGT, Arg to Ser) in hepatocellular carcinoma (HCC) makes this mutation an indirect indicator of dietary contamination with this toxin.
|
23649769 |
2013 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Although its metabolites bind at several positions in TP53, a mutation at codon 249 (AGG to AGT, arginine to serine, p.R249S) accounts for 90% of TP53 mutations in AFB(1)-related HCC.
|
20538734 |
2010 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
To investigate whether human angiotensinogen protects against tumor progression in vivo, we established an original bitransgenic model in which transgenic mice expressing human angiotensinogen (Hu-AGT-TG mice) were crossed with a transgenic mouse model of hepatocellular carcinoma (HCC-TG mice).
|
19318581 |
2009 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In this study, we assessed whether the angiotensin II AT2 receptor interacting protein (ATIP)/mitochondrial tumor suppressor gene (MTUS1), a gene newly identified at position 8p22, may be a candidate tumor suppressor gene mutated in HCC.
|
16650523 |
2006 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Since a crosstalk between AGE and angiotensin II (Ang II) has been proposed in the pathogenesis of accelerated atherosclerosis in diabetes, we examined here whether and how telmisartan, a unique Ang II type 1 receptor blocker (ARB) with peroxisome proliferator-activated receptor-gamma (PPAR-gamma)-modulating activity, could inhibit AGE-induced CRP expression in a human hepatoma cell line, Hep3B cells.
|
17004092 |
2006 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Hepatocellular carcinoma (HCC) from regions with high dietary exposure to aflatoxins and endemic for hepatitis B virus (HBV) often contain a specific mutation at codon 249 in TP53 (249(ser); AGG to AGT, Arg to Ser).
|
16007211 |
2005 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
A selective mutation in TP53 (AGG-->AGT at codon 249, Arg-->Ser) has been identified as a hotspot in HCCs from such areas, reflecting DNA damage caused by aflatoxin metabolites.
|
15095302 |
2004 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
AGG to AGT transversion in codon 249 of exon 7 of the p53 gene occurs in over 50% of HCC from endemic regions, where both chronic infection with the hepatitis B virus (HBV) and exposure to carcinogens such as aflatoxin B1 (AFB1) prevail.
|
10856831 |
2000 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The most frequent mutation of the p53 gene in HCC is an AGG(Arg) to AGT(Ser) missense mutation at codon 249 of exon 7.
|
10738214 |
2000 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
We also show that transcriptional activity of reporter constructs containing human angiotensinogen gene promoter with nucleoside A at -20 is increased on cotransfection of an expression vector containing human estrogen receptor-alpha coding sequence in human hepatoma cells (HepG2) followed by estrogen treatment.
|
9931090 |
1999 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
In the present study, we analyzed the human angiotensinogen proximal promoter region by means of Chloramphenicol acetyltransferase assays, and suggested that the region from -106 to +44 is sufficient for hepatoma cell line (HepG2)-specific expression.
|
9266849 |
1997 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
AGG to AGT mutations in codon 249 of the p53 tumor-suppressor gene are frequently observed in hepatocellular carcinomas (HCC) from areas where exposure to aflatoxin B1 (AFB) occurs.
|
8895534 |
1996 |
Liver carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Fifty-eight percent of hepatocellular carcinomas (HCCs) from Qidong, China, contain an AGG to AGT mutation at codon 249 of the p53 tumor suppressor gene, a mutation that is rarely seen in HCCs from Western countries.
|
8191284 |
1994 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Our results indicate that angiotensinogen mRNA is present in human hepatoma (HepG2) cells and its levels are decreased when treated with hepatocyte stimulating factor.
|
2824952 |
1987 |