HCSGD entry for TGFBI


1. General information

Official gene symbolTGFBI
Entrez ID7045
Gene full nametransforming growth factor, beta-induced, 68kDa
Other gene symbolsBIGH3 CDB1 CDG2 CDGG1 CSD CSD1 CSD2 CSD3 EBMD LCD1
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0001525AngiogenesisIEPbiological_process
GO:0002062Chondrocyte differentiationIEAbiological_process
GO:0005178Integrin bindingTASmolecular_function
GO:0005576Extracellular regionTAScellular_component
GO:0005604Basement membraneIEAcellular_component
GO:0005615Extracellular spaceIEAcellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0007155Cell adhesionIEAbiological_process
GO:0007162Negative regulation of cell adhesionTASbiological_process
GO:0007601Visual perceptionIEAbiological_process
GO:0008283Cell proliferationTASbiological_process
GO:0030198Extracellular matrix organizationIEAbiological_process
GO:0031012Extracellular matrixIDA ISScellular_component
GO:0050840Extracellular matrix bindingIEAmolecular_function
GO:0050896Response to stimulusIEAbiological_process
GO:0070062Extracellular vesicular exosomeIDAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.26628848830.27170637510.96224317680.9968753136

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.0537910430
GSE13712_SHEARUp0.9383889728
GSE13712_STATICUp1.2534690860
GSE19018Up0.3272692728
GSE19899_A1Up0.2229731837
GSE19899_A2Down-0.3256183557
PubMed_21979375_A1Down-0.6045028847
PubMed_21979375_A2Down-0.0610174303
GSE35957Down-0.3709466650
GSE36640Up0.0499543058
GSE54402Down-0.1147883404
GSE9593Up0.1215259543
GSE43922Up0.1982831462
GSE24585Up0.0245385238
GSE37065Up0.0711706269
GSE28863_A1Down-0.2315957673
GSE28863_A2Down-0.0752595381
GSE28863_A3Down-0.0483286073
GSE28863_A4Down-0.4962540190
GSE48662Down-0.1971974079

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-21-5pMIMAT0000076MIRT001208Luciferase reporter assay//Western blotFunctional MTI19136465
hsa-miR-21-5pMIMAT0000076MIRT001208MicroarrayFunctional MTI (Weak)18591254
hsa-miR-9-5pMIMAT0000441MIRT006894In situ hybridization//Luciferase reporter assayFunctional MTI21720722
hsa-miR-30a-5pMIMAT0000087MIRT028431ProteomicsFunctional MTI (Weak)18668040
hsa-miR-26b-5pMIMAT0000083MIRT028995MicroarrayFunctional MTI (Weak)19088304
hsa-miR-16-5pMIMAT0000069MIRT031494ProteomicsFunctional MTI (Weak)18668040
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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: 1 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22695319The role of TGFBI in mesothelioma and breast cancer: association with tumor suppression
22695319BACKGROUND: Transforming growth factor beta induced (TGFBI) product, an extracellular matrix (ECM) protein, has been implicated as a putative tumor suppressor in recent studies
22695319Our previous findings revealed that expression of TGFBI gene is down-regulated in a variety of cancer cell lines and clinical tissue samples
22695319In this study, ectopic expression of TGFBI was used to ascertain its role as a tumor suppressor and to determine the underlying mechanism of mesothelioma and breast cancer
22695319Ectopic expression of TGFBI was quantified by using quantitative PCR and Western-blotting
22695319RESULTS: In this study, an ectopic expression of TGFBI in two types of cancer cell lines, a mesothelioma cell line NCI-H28 and a breast cancer cell line MDA-MB-231 was found to have reduced the cellular growth, plating efficiency, and anchorage-independent growth
22695319The tumorigenicity of these cancer cell lines as determined by subcutaneous inoculation in nude mice was similarly suppressed by TGFBI expression
22695319Likewise, TGFBI expression reduced the proportion of S-phase while increased the proportion of G1 phase in these cells
22695319The redistribution of cell cycle phase after re-expression of TGFBI was correspondent with transiently elevated expression of p21 and p53
22695319CONCLUSION: Collectively, these results imply that TGFBI plays a suppressive role in the development of mesothelioma and breast cancer cells, possibly through inhibitions of cell proliferation, delaying of G1-S phase transition, and induction of senescence
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