HCSGD entry for TGFA
1. General information
Official gene symbol | TGFA |
---|---|
Entrez ID | 7039 |
Gene full name | transforming growth factor, alpha |
Other gene symbols | TFGA |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

This gene isn't in Literature mining network.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000165 | MAPK cascade | IDA | biological_process |
GO:0000187 | Activation of MAPK activity | IDA | biological_process |
GO:0001525 | Angiogenesis | IEA | biological_process |
GO:0001948 | Glycoprotein binding | IEA | molecular_function |
GO:0004708 | MAP kinase kinase activity | IDA | molecular_function |
GO:0005154 | Epidermal growth factor receptor binding | IDA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005615 | Extracellular space | IDA | cellular_component |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005886 | Plasma membrane | NAS | cellular_component |
GO:0006468 | Protein phosphorylation | IDA | biological_process |
GO:0007173 | Epidermal growth factor receptor signaling pathway | IEA | biological_process |
GO:0008083 | Growth factor activity | IDA | molecular_function |
GO:0008152 | Metabolic process | IDA | biological_process |
GO:0008283 | Cell proliferation | TAS | biological_process |
GO:0009986 | Cell surface | IDA | cellular_component |
GO:0016021 | Integral component of membrane | IEA | cellular_component |
GO:0016310 | Phosphorylation | IDA | biological_process |
GO:0016323 | Basolateral plasma membrane | IDA | cellular_component |
GO:0031410 | Cytoplasmic vesicle | IDA | cellular_component |
GO:0042060 | Wound healing | IEA | biological_process |
GO:0042493 | Response to drug | IEA | biological_process |
GO:0043066 | Negative regulation of apoptotic process | IEA | biological_process |
GO:0045741 | Positive regulation of epidermal growth factor-activated receptor activity | IDA | biological_process |
GO:0045840 | Positive regulation of mitosis | IDA | biological_process |
GO:0048471 | Perinuclear region of cytoplasm | IDA | cellular_component |
GO:0050679 | Positive regulation of epithelial cell proliferation | IDA | biological_process |
GO:0051781 | Positive regulation of cell division | IEA | biological_process |
GO:0060749 | Mammary gland alveolus development | 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 |
---|---|---|---|
0.0492572509 | 0.9677161088 | 0.4882649813 | 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 | 0.5285817182 |
GSE13712_SHEAR | Down | -0.0433444251 |
GSE13712_STATIC | Up | 0.0678636530 |
GSE19018 | Up | 0.1557099417 |
GSE19899_A1 | Up | 0.1039870576 |
GSE19899_A2 | Up | 0.9518687496 |
PubMed_21979375_A1 | Up | 0.9943691899 |
PubMed_21979375_A2 | Up | 0.3043185052 |
GSE35957 | Down | -0.0774514197 |
GSE36640 | Up | 0.2981388551 |
GSE54402 | Up | 0.6075522254 |
GSE9593 | Down | -0.0738254464 |
GSE43922 | Up | 0.0175969219 |
GSE24585 | Up | 0.3375965165 |
GSE37065 | Up | 0.0014860211 |
GSE28863_A1 | Down | -0.3216558038 |
GSE28863_A2 | Up | 0.0445643034 |
GSE28863_A3 | Up | 0.1636551769 |
GSE28863_A4 | Up | 0.0709731596 |
GSE48662 | Up | 0.0868522402 |
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-152-3p | MIMAT0000438 | MIRT035552 | Luciferase reporter assay | Functional MTI | 23460133 |
hsa-miR-92a-3p | MIMAT0000092 | MIRT049451 | CLASH | Functional MTI (Weak) | 23622248 |
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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: 3 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
12593448 | The role of epidermal growth factors (EGF) and transforming growth factors (TGF) alpha and beta as autocrine factors in inducing senescence of cultured HMEC cells were also investigated |
12593448 | Supplementation of growth media by TGF-alpha induced significant increase in proliferation of target cells |
12593448 | Addition of epidermal growth factors receptor (EGFR) antibody to cells exposed to media devoid of EGF and media supplemented with TGF-alpha showed marked suppression of proliferation of target cells |
12593448 | The morphologic and phenotypic characteristics of target HMEC cells exposed to TGF-alpha were also found similar to those HMEC cells grown during primary culture, suggesting autocrine production of EGF and TGF-alpha by cultured HMEC cells during primary culture |
12593448 | Exposure of senescent cells to media supplemented with EGF and TGF-alpha could not induce their proliferation |
7778920 | This effect is most likely mediated by cytokines that stimulate keratinocyte growth, such as transforming growth factor alpha |
7778920 | In this study, transforming growth factor alpha gene expression in cultured foreskin keratinocytes from donors varying in age from 2 to 82 years was analyzed semiquantitatively by two separate methods, ie, Northern hybridization and competitive polymerase chain reaction |
7778920 | RESULTS: No pattern of decline in transforming growth factor alpha messenger RNA expression with increasing cellular age was observed by either analysis |
7778920 | CONCLUSION: The results indicate that expression of transforming growth factor alpha by cultured grafts may not be significantly affected by increasing cellular age and suggest that, even in the elderly, cultured autografts may be effective as pharmacologic agents for wound treatment |
8504493 | Autocrine production of TGF-alpha and TGF-beta during tumour progression of rat oral keratinocytes |
8504493 | This study describes a new technique to separate transforming growth factor-alpha (TGF-alpha) and transforming growth factor-beta (TGF-beta) from culture supernatants using ion exchange chromatography; assays of competitive inhibition of ligand binding were used to quantify the amount of growth factor |
8504493 | The autocrine production of TGF-alpha and TGF-beta was examined in oral keratinocyte cell lines derived from the palatal and lingual mucosa of rats painted with the carcinogen 4-nitroquinoline N-oxide (4NQO) |
8504493 | Escape from cellular senescence (immortality) was associated with a marked increase in TGF-alpha production (cell line R2P) but tumour progression, as reflected by the development of anchorage independence in agarose gels and tumorigenicity in athymic mice, did not result in a consistent increase or decrease of TGF-alpha production compared to normals |
8504493 | Four cell lines (R8AP, R1T, R3T, R1P), with different functional cellular phenotypes, produced two to three times more TGF-alpha than normals |
8504493 | TGF-alpha production was inversely correlated to epidermal growth factor cell surface receptor expression |
8504493 | The production of TGF-beta was unrelated to tumour progression, the expression of TGF-beta cell surface receptors or TGF-alpha production |
8504493 | The results indicate that the autocrine production of TGF-alpha and TGF-beta are not accurate markers of tumour progression in the rat 4NQO model of oral carcinogenesis |
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