HCSGD entry for CTGF
1. General information
Official gene symbol | CTGF |
---|---|
Entrez ID | 1490 |
Gene full name | connective tissue growth factor |
Other gene symbols | CCN2 HCS24 IGFBP8 NOV2 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0001502 | Cartilage condensation | IEA | biological_process |
GO:0001503 | Ossification | IEA | biological_process |
GO:0001525 | Angiogenesis | IEA | biological_process |
GO:0001558 | Regulation of cell growth | IEA | biological_process |
GO:0001934 | Positive regulation of protein phosphorylation | IEA | biological_process |
GO:0001968 | Fibronectin binding | IEA | molecular_function |
GO:0005178 | Integrin binding | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005520 | Insulin-like growth factor binding | IEA | molecular_function |
GO:0005576 | Extracellular region | TAS | cellular_component |
GO:0005578 | Proteinaceous extracellular matrix | IEA | cellular_component |
GO:0005615 | Extracellular space | IEA | cellular_component |
GO:0005794 | Golgi apparatus | IDA | cellular_component |
GO:0005801 | Cis-Golgi network | IEA | cellular_component |
GO:0005829 | Cytosol | IEA | cellular_component |
GO:0005886 | Plasma membrane | TAS | cellular_component |
GO:0005938 | Cell cortex | IEA | cellular_component |
GO:0006260 | DNA replication | IEA | biological_process |
GO:0006367 | Transcription initiation from RNA polymerase II promoter | TAS | biological_process |
GO:0007160 | Cell-matrix adhesion | IEA | biological_process |
GO:0007229 | Integrin-mediated signaling pathway | IEA | biological_process |
GO:0008083 | Growth factor activity | IEA | molecular_function |
GO:0008201 | Heparin binding | IEA | molecular_function |
GO:0008284 | Positive regulation of cell proliferation | IEA | biological_process |
GO:0008543 | Fibroblast growth factor receptor signaling pathway | IEA | biological_process |
GO:0008544 | Epidermis development | TAS | biological_process |
GO:0009611 | Response to wounding | TAS | biological_process |
GO:0009749 | Response to glucose | IEA | biological_process |
GO:0010260 | Organ senescence | IEA | biological_process |
GO:0010467 | Gene expression | TAS | biological_process |
GO:0010628 | Positive regulation of gene expression | IEA | biological_process |
GO:0010629 | Negative regulation of gene expression | IEA | biological_process |
GO:0010942 | Positive regulation of cell death | IEA | biological_process |
GO:0016477 | Cell migration | IEA | biological_process |
GO:0030154 | Cell differentiation | IEA | biological_process |
GO:0030324 | Lung development | IEA | biological_process |
GO:0032330 | Regulation of chondrocyte differentiation | IEA | biological_process |
GO:0032355 | Response to estradiol | IEA | biological_process |
GO:0032967 | Positive regulation of collagen biosynthetic process | IEA | biological_process |
GO:0034059 | Response to anoxia | IEA | biological_process |
GO:0035556 | Intracellular signal transduction | IEA | biological_process |
GO:0035988 | Chondrocyte proliferation | IEA | biological_process |
GO:0043200 | Response to amino acid | IEA | biological_process |
GO:0043231 | Intracellular membrane-bounded organelle | IDA | cellular_component |
GO:0043280 | Positive regulation of cysteine-type endopeptidase activity involved in apoptotic process | IEA | biological_process |
GO:0043434 | Response to peptide hormone | IEA | biological_process |
GO:0044255 | Cellular lipid metabolic process | TAS | biological_process |
GO:0044281 | Small molecule metabolic process | TAS | biological_process |
GO:0045597 | Positive regulation of cell differentiation | IDA | biological_process |
GO:0046330 | Positive regulation of JNK cascade | IDA | biological_process |
GO:0048471 | Perinuclear region of cytoplasm | IEA | cellular_component |
GO:0050867 | Positive regulation of cell activation | IEA | biological_process |
GO:0051385 | Response to mineralocorticoid | IEA | biological_process |
GO:0051496 | Positive regulation of stress fiber assembly | IDA | biological_process |
GO:0060401 | Cytosolic calcium ion transport | IEA | biological_process |
GO:0060452 | Positive regulation of cardiac muscle contraction | IEA | biological_process |
GO:0060548 | Negative regulation of cell death | IEA | biological_process |
GO:0070278 | Extracellular matrix constituent secretion | IEA | biological_process |
GO:0070318 | Positive regulation of G0 to G1 transition | IEA | biological_process |
GO:0070374 | Positive regulation of ERK1 and ERK2 cascade | IDA | biological_process |
GO:0070542 | Response to fatty acid | IEA | biological_process |
GO:0072593 | Reactive oxygen species metabolic process | IEA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.8292028456 | 0.0042957790 | 0.9999902473 | 0.1334937426 |
- 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 | Down | -0.3987664600 |
GSE13712_SHEAR | Up | 0.6890184169 |
GSE13712_STATIC | Down | -0.0731687377 |
GSE19018 | Down | -0.2038056339 |
GSE19899_A1 | Down | -0.7568638950 |
GSE19899_A2 | Down | -1.0825106050 |
PubMed_21979375_A1 | Down | -1.4757457885 |
PubMed_21979375_A2 | Down | -0.9987206339 |
GSE35957 | Up | 0.7636726258 |
GSE36640 | Up | 0.1024311880 |
GSE54402 | Down | -1.4327168174 |
GSE9593 | Up | 0.6360869542 |
GSE43922 | Down | -0.6364210912 |
GSE24585 | Up | 0.0324808887 |
GSE37065 | Down | -0.5047901287 |
GSE28863_A1 | Down | -0.2910762417 |
GSE28863_A2 | Down | -0.1550348956 |
GSE28863_A3 | Up | 0.4032655182 |
GSE28863_A4 | Down | -0.4094894163 |
GSE48662 | Down | -0.1828207457 |
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-124-3p | MIMAT0000422 | MIRT002604 | Microarray | Functional MTI (Weak) | 15685193 |
hsa-miR-124-3p | MIMAT0000422 | MIRT002604 | Microarray | Functional MTI (Weak) | 18668037 |
hsa-miR-18a-5p | MIMAT0000072 | MIRT004174 | Western blot//Microarray//Northern blot//Luciferase reporter assay | Functional MTI | 16331254 |
hsa-miR-18a-5p | MIMAT0000072 | MIRT004174 | Luciferase reporter assay | Functional MTI | 19233176 |
hsa-miR-26a-5p | MIMAT0000082 | MIRT004338 | Western blot | Non-Functional MTI | 18713946 |
hsa-miR-205-5p | MIMAT0000266 | MIRT006936 | Western blot | Functional MTI | 23056551 |
hsa-miR-145-5p | MIMAT0000437 | MIRT007247 | Luciferase reporter assay | Functional MTI | 23390502 |
hsa-miR-375 | MIMAT0000728 | MIRT019692 | Microarray | Functional MTI (Weak) | 20215506 |
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- mirRecord
MicroRNA name | mirBase ID | Target site number | MiRNA mature ID | Test method inter | MiRNA regulation site | Reporter target site | Pubmed ID |
---|---|---|---|---|---|---|---|
hsa-miR-19a-3p | MIMAT0000073 | NA | hsa-miR-19a | 20305691 | |||
hsa-miR-19b-3p | MIMAT0000074 | NA | hsa-miR-19b | 20305691 |
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6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 6 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
23155386 | Expression of apolipoprotein J (Apo J), connective tissue growth factor (CTGF), fibronectin, and laminin were examined by real-time PCR, western blot, or ELISA experiments |
23155386 | Exposure to 8% of CSE markedly increased the number of SA-ss-Gal positive cells to up to 82%, and the mRNA expression of Apo J, CTGF, and fibronectin by approximately 3-4 fold |
23155386 | Treatment with 8% of CSE also increased the protein expression of Apo J and CTGF and the secretion of fibronectin and laminin |
22319624 | Omega-6 increased fibronectin and connective tissue growth factor synthesis, as well as the amount of secreted fibronectin |
22319624 | H(2)O(2) stimulation of plasminogen activator inhibitor 1 and connective tissue growth factor was repressed by both fatty acids |
19730126 | Postinfarct cardiac remodeling was associated with increased atrial natriuretic peptide, interleukin-6 and connective tissue growth factor mRNA expressions, as well as three-fold increased cardiomyocyte senescence, measured as cardiac p16 mRNA expression |
19730126 | Levosimendan also ameliorated MI-induced atrial natriuretic peptide, IL-6, and connective tissue growth factor overexpression as well as MI-induced disturbances in calcium-handling proteins (SERCA2, Na-Ca exchanger) without changes in diabetic status or systemic blood pressure |
19171648 | Expression of senescence-associated genes (apolipoprotein J [Apo J], connective tissue growth factor [CTGF], fibronectin, and SM22) was examined by real-time PCR and induction of signal transduction proteins (p21, p16, and pRb) by Western blot analysis |
19171648 | RESULTS: H(2)O(2) markedly increased the number of SA-beta-Gal-positive cells to up to 89% and the expression of Apo J, CTGF, fibronectin, and SM22 by approximately three to fourfold |
15610763 | Pyruvate dehydrogenase kinase 3 (Pdk3) and connective tissue growth factor (Ctgf) were up-regulated and hyaluronan synthase 3 (Has3) down-regulated under both conditions |
15147944 | Expression of connective tissue growth factor, a biomarker in senescence of human diploid fibroblasts, is up-regulated by a transforming growth factor-beta-mediated signaling pathway |
15147944 | Proteome analysis data demonstrated that connective tissue growth factor (CTGF) is an age-associated protein |
15147944 | Up-regulation of CTGF expression in senescent cells was further confirmed by Western blotting and RT-PCR |
15147944 | We postulate that CTGF expression is controlled, in part, by transforming growth factor-beta (TGF-beta), in view of the high levels of TGF-beta isoforms as well as type I and II receptors detected only in late PDL of HDF cells |
15147944 | As expected, CTGF expression and Smad protein phosphorylation were dramatically increased up to observed levels in normal replicative senescent cells |
15147944 | In vivo experiments disclosed that CTGF, pSmad, and p53 were constitutively expressed at basal levels in up to 18-month-old rat liver, and expression was significantly up-regulated in 24-month-old rat tissue |
15147944 | In view of both in vitro and in vivo data, we propose that the TGF-beta/Smad pathway functions in the induction of CTGF, a novel biomarker protein of cellular senescence in human fibroblasts |
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