HCSGD entry for LGALS3
1. General information
Official gene symbol | LGALS3 |
---|---|
Entrez ID | 3958 |
Gene full name | lectin, galactoside-binding, soluble, 3 |
Other gene symbols | CBP35 GAL3 GALBP GALIG L31 LGALS2 MAC2 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

This gene isn't in PPI subnetwork.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0001501 | Skeletal system development | IEA | biological_process |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005578 | Proteinaceous extracellular matrix | IEA | cellular_component |
GO:0005634 | Nucleus | IDA IEA | cellular_component |
GO:0005681 | Spliceosomal complex | IEA | cellular_component |
GO:0005737 | Cytoplasm | IDA IEA | cellular_component |
GO:0005743 | Mitochondrial inner membrane | IDA | cellular_component |
GO:0005886 | Plasma membrane | TAS | cellular_component |
GO:0006397 | MRNA processing | IEA | biological_process |
GO:0008380 | RNA splicing | IEA | biological_process |
GO:0019863 | IgE binding | IEA | molecular_function |
GO:0030154 | Cell differentiation | IEA | biological_process |
GO:0030198 | Extracellular matrix organization | IEA | biological_process |
GO:0030246 | Carbohydrate binding | IEA | molecular_function |
GO:0031012 | Extracellular matrix | IDA | cellular_component |
GO:0045087 | Innate immune response | TAS | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.3314509365 | 0.5737212454 | 0.9999902473 | 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 | 0.0960146659 |
GSE13712_SHEAR | Down | -0.2725621666 |
GSE13712_STATIC | Down | -0.1502232074 |
GSE19018 | Up | 0.0133598344 |
GSE19899_A1 | Up | 0.0197011288 |
GSE19899_A2 | Down | -0.4152842459 |
PubMed_21979375_A1 | Up | 0.1512747121 |
PubMed_21979375_A2 | Up | 0.2504428038 |
GSE35957 | Down | -0.1384641842 |
GSE36640 | Up | 0.0169503910 |
GSE54402 | Down | -0.3737900220 |
GSE9593 | Up | 0.4931428499 |
GSE43922 | Down | -0.0638667374 |
GSE24585 | Up | 0.1995999962 |
GSE37065 | Up | 0.1693033743 |
GSE28863_A1 | Up | 0.0895387999 |
GSE28863_A2 | Up | 0.3727785190 |
GSE28863_A3 | Down | -0.3976156300 |
GSE28863_A4 | Up | 0.3010285255 |
GSE48662 | Up | 0.1447695372 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
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- Drugs
Name | Drug | Accession number |
---|---|---|
2,3,5,6-Tetrafluoro-4-Methoxy-Benzamide | DB01827 | EXPT00667 |
- MicroRNAs
- mirTarBase
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-424-3p | MIMAT0004749 | MIRT003969 | Northern blot//qRT-PCR//Western blot | Functional MTI | 17889671 |
hsa-miR-744-5p | MIMAT0004945 | MIRT037600 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
- mirRecord
MicroRNA name | mirBase ID | Target site number | MiRNA mature ID | Test method inter | MiRNA regulation site | Reporter target site | Pubmed ID |
---|---|---|---|---|---|---|---|
hsa-miR-424-3p | MIMAT0004749 | 1 | hsa-miR-424* | {Western blot} | {underexpression by 2'-O-Me antisense miRNA oligonucleotides} | 17889671 |
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6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26273429 | Senescent mesenchymal stem cells promote colorectal cancer cells growth via galectin-3 expression |
26273429 | Analysis of the factors secreted in the MSCs culture media determined that senescent MSCs expressed and secreted high levels of galectin-3 |
26273429 | Furthermore, the simultaneous addition of recombinant galectin-3 to the co-culture systems partially restored the tumor-promoting effect of the senescent AD-MSCs |
26273429 | Analysis of the mechanisms of senescent MSCs and galectin-3 on LoVo cells signal transduction determined that senescent MSCs and exogenous galectin-3 promoted cell growth by activating the mitogen-activated protein kinase (MAPK) (extracellular signal-regulated kinase [ERK]1/2) pathway |
26273429 | CONCLUSIONS: Senescent MSCs may alter the tissue microenvironment and affect nearby malignant cells via cytokine secretion, and galectin-3 is an important mediator of senescent AD-MSC-mediated stimulation of colon cancer cell growth |
19492299 | High-resolution two-dimensional electrophoresis of the MSC proteome, under conditions of in vitro self-renewal as well as osteogenic stimulation, identified several age-dependent proteins, including members of the calponin protein family as well as galectin-3 |
10694443 | In the LG1 strain of human diploid fibroblasts, galectin-3 could be found in both the nucleus and the cytoplasm of young, proliferating cells |
10694443 | Incubation of young cells with leptomycin B, a drug that disrupts the interaction between the leucine-rich nuclear export signal and its receptor, resulted in the accumulation of galectin-3 inside the nucleus |
10694443 | In senescent cells, galectin-3 staining remained cytoplasmic even in the presence of the drug, thus suggesting that the observed localization in the cytoplasm was due to a lack of nuclear import |
10694443 | In heterodikaryons derived from fusion of young and senescent LG1 cells, the predominant phenotype was galectin-3 in both nuclei |
10694443 | These results suggest that senescent LG1 cells might lack a factor(s) specifically required for galectin-3 nuclear import |
9439577 | The human LGALS3 (galectin-3) gene: determination of the gene structure and functional characterization of the promoter |
9439577 | Here we report the genomic organization of the human LGALS3 (galectin-3) gene and functional characterization of the promoter |
9439577 | Southern blot analysis of genomic DNA revealed that galectin-3 is coded by a single gene in the human genome |
9439577 | Because galectin-3 is an immediate-early gene whose expression is dependent on the proliferative state of the cell, this study provides the basis for determining the molecular mechanisms of transcriptional regulation in neoplasia or cellular senescence |
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