HCSGD entry for CASP9
1. General information
Official gene symbol | CASP9 |
---|---|
Entrez ID | 842 |
Gene full name | caspase 9, apoptosis-related cysteine peptidase |
Other gene symbols | APAF-3 APAF3 ICE-LAP6 MCH6 PPP1R56 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
![color bar](img/red_blue.jpg)
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0004197 | Cysteine-type endopeptidase activity | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005622 | Intracellular | IEA | cellular_component |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005739 | Mitochondrion | IEA | cellular_component |
GO:0005829 | Cytosol | IDA IEA TAS | cellular_component |
GO:0006508 | Proteolysis | IEA | biological_process |
GO:0006915 | Apoptotic process | IEA TAS | biological_process |
GO:0006919 | Activation of cysteine-type endopeptidase activity involved in apoptotic process | IEA | biological_process |
GO:0006974 | Cellular response to DNA damage stimulus | IDA IEA | biological_process |
GO:0007173 | Epidermal growth factor receptor signaling pathway | TAS | biological_process |
GO:0007568 | Aging | IEA | biological_process |
GO:0008047 | Enzyme activator activity | TAS | molecular_function |
GO:0008233 | Peptidase activity | IDA | molecular_function |
GO:0008543 | Fibroblast growth factor receptor signaling pathway | TAS | biological_process |
GO:0008630 | Intrinsic apoptotic signaling pathway in response to DNA damage | IMP | biological_process |
GO:0008635 | Activation of cysteine-type endopeptidase activity involved in apoptotic process by cytochrome c | TAS | biological_process |
GO:0009411 | Response to UV | IEA | biological_process |
GO:0017124 | SH3 domain binding | IDA | molecular_function |
GO:0019901 | Protein kinase binding | IDA | molecular_function |
GO:0030220 | Platelet formation | TAS | biological_process |
GO:0032025 | Response to cobalt ion | IEA | biological_process |
GO:0032355 | Response to estradiol | IEA | biological_process |
GO:0032496 | Response to lipopolysaccharide | IEA | biological_process |
GO:0034349 | Glial cell apoptotic process | IEA | biological_process |
GO:0034644 | Cellular response to UV | IDA | biological_process |
GO:0038095 | Fc-epsilon receptor signaling pathway | TAS | biological_process |
GO:0042770 | Signal transduction in response to DNA damage | IDA | biological_process |
GO:0042981 | Regulation of apoptotic process | IEA TAS | biological_process |
GO:0043065 | Positive regulation of apoptotic process | TAS | biological_process |
GO:0043293 | Apoptosome | IDA | cellular_component |
GO:0043525 | Positive regulation of neuron apoptotic process | IEA | biological_process |
GO:0045087 | Innate immune response | TAS | biological_process |
GO:0046677 | Response to antibiotic | IEA | biological_process |
GO:0048011 | Neurotrophin TRK receptor signaling pathway | TAS | biological_process |
GO:0048015 | Phosphatidylinositol-mediated signaling | TAS | biological_process |
GO:0071549 | Cellular response to dexamethasone stimulus | IEA | biological_process |
GO:0097193 | Intrinsic apoptotic signaling pathway | TAS | biological_process |
GO:2001020 | Regulation of response to DNA damage stimulus | IMP | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.1305199233 | 0.8921748870 | 0.7337494447 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.0857318879 |
GSE13712_SHEAR | Up | 0.3476060764 |
GSE13712_STATIC | Up | 0.3817753667 |
GSE19018 | Up | 0.1690628598 |
GSE19899_A1 | Up | 0.0325970199 |
GSE19899_A2 | Up | 0.6475398515 |
PubMed_21979375_A1 | Up | 0.6799438120 |
PubMed_21979375_A2 | Up | 0.2205824006 |
GSE35957 | Up | 0.0591891740 |
GSE36640 | Up | 0.0886573959 |
GSE54402 | Up | 0.1895777811 |
GSE9593 | Up | 0.0455671169 |
GSE43922 | Up | 0.2562374677 |
GSE24585 | Up | 0.3149713735 |
GSE37065 | Down | -0.0904077391 |
GSE28863_A1 | Down | -0.0193769948 |
GSE28863_A2 | Down | -0.0817272652 |
GSE28863_A3 | Down | -0.4443510297 |
GSE28863_A4 | Down | -0.1903336133 |
GSE48662 | Down | -0.3062615614 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-133a-3p | MIMAT0000427 | MIRT001986 | Luciferase reporter assay | Functional MTI | 17715156 |
hsa-let-7a-5p | MIMAT0000062 | MIRT005294 | Western blot | Non-Functional MTI | 18758960 |
hsa-miR-193b-3p | MIMAT0002819 | MIRT016408 | Microarray | Functional MTI (Weak) | 20304954 |
hsa-miR-7-5p | MIMAT0000252 | MIRT025767 | Microarray | Functional MTI (Weak) | 19073608 |
hsa-miR-26b-5p | MIMAT0000083 | MIRT029244 | Microarray | Functional MTI (Weak) | 19088304 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 12 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
27212655 | This resistance occurred via caspase-9 and caspase-3 rather than via caspase-8 |
26515130 | Ad5-CMV-CCN1 induced HSC apoptosis that was evident by proteolytic cleavage of caspase-12, caspase-9 and the executor caspase-3 and positive TUNEL stain |
25962658 | Quantitative analysis of the expression of caspase 3 and caspase 9 in different types of atherosclerotic lesions in the human aorta |
25962658 | This study was undertaken to evaluate the levels of the expression of key apoptosis-related genes, namely, caspase 3 (CASP3) and caspase 9 (CASP9) in the normal (non-atherosclerotic) intima of the human aorta in comparison with those in different types of atherosclerotic lesions |
25962658 | The study revealed that the expressions of CASP3 and CASP9 genes were changed in different types of atherosclerotic lesions in course of the progression of the disease, but not in a unanimous way |
25962658 | Our study provides novel quantitative data on the expression of CASP3 and CASP9 genes in different atherosclerotic lesions in the human aorta and thus, might assist in better understanding of the processes occurring during the development of lesions in human atherogenesis |
25852816 | Cell senescence was found to appear prematurely in DS cells as shown by SA-beta-Gal assay and p21 assessment, though not apoptosis, as neither p53 nor the proapoptotic proteins cytochrome c and caspase 9 were altered in T21F |
24782600 | Activation of egr-1, in turn, upregulates the dual specificity phosphatase, phosphatase and tensin homologue deleted on chromosome ten (PTEN) resulting in activation of pro-apoptotic caspase-3 and caspase-9 and reduced expression of the anti-apoptosis protein, survivin |
24535104 | In the present study, RC-6 induced cytotoxicity in NT2 cells (a human embryonal carcinoma cell line) and our studies showed that RC-6 can exert anticancer effects and induce caspase-9 and -3 activities |
23238821 | The apoptosis and senescence of NP cells was investigated by terminal deoxyribonucleotidyl transferase (TDT)-mediated dUTP-digoxigenin nick end labeling (TUNEL) assay, immunohistochemistry, and Western blot for caspase3, caspase8, caspase9, and p16lnk4A (increased in cellular senescence) |
22919441 | Both SIPS and senescent HDFs shared similar apoptotic changes such as increased Annexin V-FITC positive cells, increased cytochrome c release and increased activation of caspase-9 and caspase-3 (P < 0 |
22919441 | GTT treatment resulted in a significant reduction of Annexin V-FITC positive cells, inhibited cytochrome c release and decreased activation of caspase-9 and caspase-3 (P < 0 |
22919441 | These findings suggested that GTT inhibits apoptosis by modulating the upstream apoptosis cascade, causing the inhibition of cytochrome c release from the mitochondria with concomitant suppression of caspase-9 and caspase-3 activation |
18694296 | Both SAHA and MS-275 induced an arrest in the cell cycle along with the induction of apoptotic pathways as evidenced by flow cytometry, annexin assay, detection of activated caspase 9, and molecular analysis of Bax/Bcl-2 expression |
18313665 | Caspase 9 inhibition protected TRAIL-treated cells from senescence, whereas inhibition of caspases 1 and 8 increased the yield of SLP cells |
17145870 | Here, we report that IR induced caspase-9 and caspase-3 activation and subsequent apoptosis only in p21-deficient colon carcinoma cells, whereas similar treated wild-type cells were permanently arrested in the G(2)-M phase, correlating with the induction of cellular senescence |
17145870 | Interestingly, activation of the mitochondrial pathway, including caspase-2 processing, depolarization of the outer mitochondrial membrane, and cytochrome c release, was achieved by IR in both cell lines, indicating that p21 inhibits an event downstream of mitochondria but preceding caspase-9 activation |
17145870 | In addition, p21 did neither interact with caspase-3 or caspase-9, suggesting that these events are not required for the observed protection |
16325773 | Caspase-3 and caspase-9 activity was lower in Klotho-treated HUVEC than in control cells |
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