Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our study aims to identify how HSF1 confers chemoresistance through regulating metabolic pathway in hepatocellular carcinoma (HCC).
|
31815039 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
From the standpoint of therapeutic applications for hepatocellular carcinoma (HCC) treatment, HSF1 inhibition was shown to sensitize the antiproliferative effects of simvastatin in HCC cells.
|
31540279 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
However, the roles of HSF1 in the metabolic alteration of hepatocellular carcinoma (HCC) in tumor microenvironment remain elusive.
|
31497221 |
2019 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
By using the Cancer Genome Atlas (TCGA) dataset analysis, we investigated the prognosis value of HSF1 and HSF2 in HCC and identified HSF2 as a prediction factor of overall survival of HCC.
|
31497345 |
2019 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Subgroup analysis revealed that there was a significant association between HSF1 overexpression and poor prognosis in esophageal squamous cell carcinoma (ESCC) (HR=1.83; 95% CI: 1.21-2.77; <i>P</i>=0.004), breast cancer (BC) (HR=1.52; 95% CI: 1.24-2.86; <i>P</i><0.001), hepatocellular carcinoma (HR=3.02; 95% CI: 1.77-5.18; <i>P</i><0.001), non-small-cell lung cancer (HR=2.19; 95% CI: 1.20-3.99; <i>P</i>=0.01), and pancreatic cancer (HR=2.58; 95% CI: 1.11-6.03; <i>P</i>=0.03) but not in osteosarcoma (HR=1.58; 95% CI: 0.47-5.35; <i>P</i>=0.46).
|
29398920 |
2018 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
A previous study showed that HSF1 expression is associated with a poor prognosis in breast cancer and hepatocellular carcinoma; however, the prognostic significance of HSF1 in esophageal squamous cell carcinoma (ESCC) is unknown.
|
28454329 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Consequently, targeting HSF1 might represent a novel and effective therapeutic strategy for the treatment of HCC subsets with activated c-Myc signaling.
|
29207593 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Collectively, these results revealed that HSF1 elevates ATG4B via promoting its transcription, which alleviates the sensitivity of EPI in HCC cells through enhancing protective autophagy, suggesting that the "HSF1/ATG4B/protective autophagy" pathway may be a novel target for developing sensitizing strategy to HCC chemotherapy.
|
28889000 |
2017 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
In conclusion, HSF1 is an independent prognostic factor in liver cancer and might represent an innovative therapeutic target in HCC subsets characterized by activation of the AKT/mTOR pathway.
|
28903330 |
2017 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Glucose, but not 2D-glucose, can induce the phosphorylation of HSF1 at S326 and upregulate the expression of HSF1's downstream alpha B-crystallin and Hsp70 as well as the none-heat shock proteins CSK2 and RBM23 in two tested hepatocellular carcinoma cell lines (prl/prf5 and SMMC7721).
|
26010766 |
2015 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
In this study, we demonstrated that mitochondrial respiratory defects induced Cln-1 transcription via reactive oxygen species (ROS)-mediated heat shock factor 1 (HSF1) activation, which contributed to hepatoma invasiveness.
|
26157141 |
2015 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, we observed that heat shock transcription factor 1 (HSF1) directly activated miR-135b expression, consequently enhancing HCC cell motility and invasiveness.
|
25537516 |
2015 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Taken together, these data markedly support that HSF1 is a potential prognostic marker and therapeutic target for the treatment of HCC.
|
25199534 |
2014 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Chromatin immunoprecipitation (ChIP) assays demonstrated occupation of TTR promoter heat shock elements by HSF1 in APP23 hippocampi, primary murine hippocampal neurons, and SH-SY5Y cells, but not in mouse liver, cultured human hepatoma (HepG2) cells, or AC16 cultured human cardiomyocytes.
|
24849358 |
2014 |
Liver carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
To clarify the functional role of HSF1 in HCC, we established HSF1-knockdown (HSF1 KD) KYN2 HCC cells by stably expressing either small hairpin RNA (shRNA) against HSF1 (i.e.
|
24130164 |
2014 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
DNA-dependent protein kinase catalytic subunit, H2A histone family member X (H2AFX) and heat shock transcription factor-1 (HSF1) levels were assessed by immunohistochemistry and/or immunoblotting and qRT-PCR in a collection of human HCC.
|
24136149 |
2013 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Interestingly, HSF1 is highly expressed in hepatocellular carcinoma (HCC) patient samples and HCC is sensitive to combinational treatment, indicating a potential indication for the combinational treatment.
|
23615731 |
2013 |
Liver carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
We also observed that the APOBEC3B (A3B) cytidine deaminase was widely up-regulated in HCC tumor tissues; it also promoted the growth of neoplastic human HepG2 liver cells and up-regulated heat shock transcription factor1 (HSF1) expression.
|
17847074 |
2007 |