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Links from GEO DataSets

Items: 20

1.

NUPR1 a new target in liver cancer: implication in controlling cell growth, migration, invasion and sorafenib resistance

(Submitter supplied) Sorafenib, an oral multikinase inhibitor, is the only approved agent for the treatment of advanced hepatocellular carcinoma (HCC). However, its benefits is modest, also because its mechanism of action remains elusive, therefore, a better understanding of its molecular action and molecular targets are needed. On the basis of our previous studies, here, we investigated the role of the nuclear protein 1 (NUPR1) in HCC and its role in the context of sorafenib treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
2 Samples
Download data: TXT
Series
Accession:
GSE73521
ID:
200073521
2.

The chromatin protein Nupr1 regulates RelB-dependent NF-kB events necessary for pancreatic cancer development

(Submitter supplied) The objective of this study was to elucidate the role of Nupr1 in pancreatic tumorigenesis. Using the Pdx-1-cre;LSL-KrasG12D mouse as model we discovered that, in contrast to KrasG12D pancreas that develop multiple foci of pancreatic intraepithelial neoplasia (PanIN), KrasG12D;Nupr1KO pancreas were free from such lesions, indicating that Nupr1 is pivotal for PanIN formation. In vitro, MiaPaCa2 cells activated Nupr1 expression in response to nutrient deprivation and this expression was necessary for cell survival. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
14 Samples
Download data: CEL
Series
Accession:
GSE35463
ID:
200035463
3.

Re-expression of fetal IGF2 as a target for hepatocellular carcinoma therapy

(Submitter supplied) Non-coding microRNAs (miRNAs) mainly regulate the expression of targeted genes by regulating mRNA degradation or repressing their protein translation. MiRNA microarray profiling was then performed on 218 human HCC tumors samples, 10 samples from adjacent cirrhotic non-tumoral tissue, 10 samples from healthy liver and 12 HCC cell lines. In this study we investigated which miRNAs were differentially expressed in HCC compared to cirrhotic non-tumoral tissue and healthy liver.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL14613
250 Samples
Download data: CEL
Series
Accession:
GSE74618
ID:
200074618
4.

Niclosamide ethanolamine reverses gene expression and inhibits growth of hepatocellular carcinoma in vitro and in vivo

(Submitter supplied) Hepatocellular carcinoma (HCC) is a fatal malignancy with a dismal prognosis. The recent advances in genomics and transcriptomics have led to large volumes of molecular data for HCC, providing an unprecedented opportunity to translate these data into more effective therapeutics. By creating HCC gene expression signatures and comparing with drug response signatures from multiple datasets, we identified four antihelminthics (from over 1000 FDA-approved drugs) that can reverse the HCC disease gene expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
9 Samples
Download data: TXT
Series
Accession:
GSE77322
ID:
200077322
5.

Combination of celecoxib and sorafenib provides synergistic antiproliferative and proapoptotic effects in human liver cancer cells

(Submitter supplied) Molecular targeted therapy has shown promise as a treatment for advanced hepatocellular carcinoma (HCC). Sorafenib, a multikinase inhibitor, recently received FDA approval for the treatment of advanced HCC. However, although sorafenib is well tolerated, concern for its safety has been expressed. Celecoxib (Celebrex®) is a selective cyclooxygenase-2 (COX-2) inhibitor wich exhibits antitumor effects in human HCC cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE45340
ID:
200045340
6.

Sorafenib induces variations of the DNA methylome in human hepatocellular carcinoma cells.

(Submitter supplied) Sorafenib is currently the standard treatment for advanced hepatocellular carcinoma (HCC). Epigenetic alterations such as DNA methylation, play a decisive role in the development and progression of HCC. To our knowledge, there are no studies that have analyzed the global DNA methylation changes in HCC cells treated with sorafenib. Using MeDip-chip technologies we analyzed sorafenib effects on the methylome of human HCC cells. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL5082
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE72257
ID:
200072257
7.

Identification of a mitochondrial defect gene signature reveals NUPR1 as a key regulator of liver cancer progression

(Submitter supplied) Many cancer cells require more glycolytic adenosine triphosphate production due to a mitochondrial respiratory defect. However, the roles of mitochondrial defects in cancer development and progression remain unclear. To address the role of transcriptomic regulation by mitochondrial defects in liver cancer cells, we performed gene expression profiling for three different cell models of mitochondrial defects: cells with chemical respiratory inhibition (rotenone, thenoyltrifluoroacetone, antimycin A, and oligomycin), cells with mitochondrial DNA depletion (Rho0), and liver cancer cells harboring mitochondrial defects (SNU354 and SNU423). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
15 Samples
Download data: TXT
Series
Accession:
GSE64505
ID:
200064505
8.

Single Cell Analysis Reveals NUPR1 Promotes Docetaxel Resistance in Prostate Cancer

(Submitter supplied) The majority of prostate cancer (PCa) patients treated with docetaxel develop resistance to it. In order to better understand the mechanism behind the acquisition of resistance, we conducted single cell total RNA sequencing (sctotal RNA-seq) of docetaxel sensitive and resistant variants of DU145 and PC3 PCa cell lines. Overall, sensitive and resistant cells clustered separately. However, for both cell lines we identified rare sensitive cells that clustered with the resistant cells indicating resistant cells pre-exist in the sensitive population. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL20301 GPL16791
324 Samples
Download data: TXT
Series
Accession:
GSE140440
ID:
200140440
9.

NOTCH/HES5 signaling exhibits distinct roles in MYC- and AKT-driven liver carcinogenesis

(Submitter supplied) Notch signaling plays a pivotal role in liver development and aberrant Notch signaling may lead to hepatocellular (HCC) or cholangiocellular carcinoma (CCA) development. Using whole exome sequencing of 54 human HCC samples, we discovered 19 somatic missense mutations in 15 different Notch pathway genes affecting 24.6% (14 of 57) of patients. Prediction of functional impact of these Notch pathway mutations revealed HES5-R31G to have high relevance.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25683
24 Samples
Download data: CEL
Series
Accession:
GSE121362
ID:
200121362
10.

Gene expression profiling of Notch1 knockout mouse liver samples and murine hepatic angiosarcoma cell lines.

(Submitter supplied) This work is part of the paper: Generation of a murine hepatic angiosarcoma cell line and reproducible mouse tumor model, Rothweiler S et al, Laboratory Investigation, 2014 Hepatic Angiosarcoma (AS) is a rare and highly aggressive tumor of endothelial origin with dismal prognosis. Studies of the molecular biology of AS and treatment options are limited since animal models are rare. We have previously shown that inducible knockout of Notch1 in mice leads to spontaneous formation of hepatic AS. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
9 Samples
Download data: CEL
Series
Accession:
GSE57655
ID:
200057655
11.

A high-throughput screen reveals SALL4-induced oxidative phosphorylation vulnerabilities in cancer

(Submitter supplied) Transcription factors are important drivers of cancer but the development of therapeutics against these factors has had limited success. We developed a stringent high-throughput chemical genetic screening platform to identify compounds that target oncogene SALL4 dependency in liver cancer. The platform comprises SALL4 low- and high-expressing endogenous cell lines, and engineered SALL4-low isogenic lines overexpressing SALL4. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
5 Samples
Download data: TXT
12.

NUPR1 maintains autolysosomal efflux by activating SNAP25 transcription in cancer cells

(Submitter supplied) In the advanced stages of cancer, autophagy is thought to promote tumor progression through its ability to mitigate various cellular stresses. However, the details of how autophagy is homeostatically regulated in such tumors are unknown. Here, we report that NUPR1 (nuclear protein 1, transcriptional regulator), a transcriptional coregulator, is aberrantly expressed in a subset of cancer cells and predicts low overall survival rates for lung cancer patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL10999 GPL11154
4 Samples
Download data: XLS
13.

ROS stress responses of primary human epidermal keratinocytes

(Submitter supplied) Primary human epidermal keratinocytes were exposed to in-vitro UVA-oxidized 1-palmitoyl-2-arachidonoyl-phosphatidylcholine or to UVA in presence and absence of a commercial UVA filter.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
15 Samples
Download data: CEL
Series
Accession:
GSE104870
ID:
200104870
14.

Effects of HIF2α in renal cancer metastasis and sensitivity to repurposed drugs

(Submitter supplied) Background: in clear cell renal cell carcinoma (ccRCC), 80% of cases have biallelic inactivation of VHL gene, leading to constitutive activation of both HIF1α and HIF2α. As HIF2α is the driver of the disease promoting tumour growth and metastasis, drugs targeting HIF2α have been developed. However, resistance is common, therefore new therapies are needed. Methods: we generated the 786-0 HIF2α knockout (KO) cell line and assessed the HIF2α antagonist PT2385 in several steps of tumour development. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
9 Samples
Download data: CSV
15.

Human cystatin D (CST5) locates in the nucleus at sites of active transcription and regulates gene expression

(Submitter supplied) Cystatin D (CST5) is an inhibitor of several proteases of the cathepsin family that inhibits cell proliferation, migration and invasion of colon carcinoma cells. Some of these effects are unrelated to its antiprotease activity. Here, we use genome-wide expression microarrays to show that cystatin D regulates gene expression (including that of genes encoding transcription factors such as RUNX1, RUNX2, or MEF2C) in HCT116 cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16987
4 Samples
Download data: CEL
Series
Accession:
GSE45904
ID:
200045904
16.

Cell cannibalism, a cell-death process driven by the Transforming Growth Factor-β and the Nuclear Protein 1, opposes to metastasis in pancreatic cancer

(Submitter supplied) Pancreatic adenocarcinoma (PDAC) is an extremely deadly disease for which all treatments available have failed to improve life expectancy significantly. This may be explained by the high metastatic potential of PDAC cells, which results from their physiological dedifferentiation towards a mesenchymal phenotype. Some PDAC present cell-in-cell structures but their origin and significance is currently unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE38772
ID:
200038772
17.

small RNA profiling of breast cancer cell lines [knockdowns]

(Submitter supplied) We performed small RNA sequencing in breast cancer cells treated with siRNA for Control, DCGR8, DROSHA, TARBP2, DICER
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
9 Samples
Download data: BED, CNT
Series
Accession:
GSE114773
ID:
200114773
18.

Discovery and annotation of intracellular and extracellular orphan non-coding RNAs in breast cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL11154 GPL20301
68 Samples
Download data: CNT, TXT
Series
Accession:
GSE114366
ID:
200114366
19.

small RNA profiling of breast cancer cell lines

(Submitter supplied) We performed small RNA sequencing in breast cancer cells as well as human mammary epithelial cells (HUMEC) in biological replicates.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL20301
23 Samples
Download data: CNT, TXT
Series
Accession:
GSE114330
ID:
200114330
20.

small RNA profiling of extracellular RNA from breast cancer cell lines [EV]

(Submitter supplied) We performed small RNA sequencing of exosomes and extracellular vesicles collected from breast cancer cells as well as human mammary epithelial cells (HUMEC) in biological replicates (using Norgen's cell culture media exosme purification and RNA isoaltion kits).
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL20301
18 Samples
Download data: BED, CNT
Series
Accession:
GSE114329
ID:
200114329
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