HCSGD entry for GLB1
1. General information
Official gene symbol | GLB1 |
---|---|
Entrez ID | 2720 |
Gene full name | galactosidase, beta 1 |
Other gene symbols | EBP ELNR1 MPS4B |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0004553 | Hydrolase activity, hydrolyzing O-glycosyl compounds | IEA | molecular_function |
GO:0004565 | Beta-galactosidase activity | IEA TAS | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005764 | Lysosome | IEA | cellular_component |
GO:0005975 | Carbohydrate metabolic process | IEA TAS | biological_process |
GO:0006027 | Glycosaminoglycan catabolic process | TAS | biological_process |
GO:0006665 | Sphingolipid metabolic process | TAS | biological_process |
GO:0006687 | Glycosphingolipid metabolic process | TAS | biological_process |
GO:0016936 | Galactoside binding | IEA | molecular_function |
GO:0019388 | Galactose catabolic process | IEA | biological_process |
GO:0030203 | Glycosaminoglycan metabolic process | TAS | biological_process |
GO:0042339 | Keratan sulfate metabolic process | TAS | biological_process |
GO:0042340 | Keratan sulfate catabolic process | TAS | biological_process |
GO:0043202 | Lysosomal lumen | TAS | cellular_component |
GO:0044281 | Small molecule metabolic process | TAS | biological_process |
GO:0048471 | Perinuclear region of cytoplasm | IEA | cellular_component |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.9455874131 | 0.4124713309 | 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 | - | - |
GSE13712_SHEAR | - | - |
GSE13712_STATIC | - | - |
GSE19018 | - | - |
GSE19899_A1 | - | - |
GSE19899_A2 | - | - |
PubMed_21979375_A1 | - | - |
PubMed_21979375_A2 | - | - |
GSE35957 | - | - |
GSE36640 | - | - |
GSE54402 | - | - |
GSE9593 | - | - |
GSE43922 | - | - |
GSE24585 | - | - |
GSE37065 | - | - |
GSE28863_A1 | Up | 0.2837861270 |
GSE28863_A2 | Up | 0.0207793049 |
GSE28863_A3 | Down | -0.5049431232 |
GSE28863_A4 | Down | -0.3376282443 |
GSE48662 | Up | 0.1902698334 |
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-155-5p | MIMAT0000646 | MIRT020509 | Proteomics | Functional MTI (Weak) | 18668040 |
hsa-let-7b-5p | MIMAT0000063 | MIRT032234 | Proteomics | Functional 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: 6 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26391655 | Tissue-specific deletion of the essential autophagy gene Atg7 in murine VSMCs (atg7-/- VSMCs) caused accumulation of SQSTM1/p62 and accelerated the development of stress-induced premature senescence as shown by cellular and nuclear hypertrophy, CDKN2A-RB-mediated G1 proliferative arrest and senescence-associated GLB1 activity |
26391655 | Lesions of VSMC-specific atg7 knockout mice were characterized by increased total collagen deposition, nuclear hypertrophy, CDKN2A upregulation, RB hypophosphorylation, and GLB1 activity, all features typical of cellular senescence |
25876105 | Lysosomal-beta-galactosidase (GLB1) hydrolyzes beta-galactose from glycoconjugates and is the origin of senescence-associated beta-gal activity (SA-beta-gal) |
25876105 | Using a new GLB1 antibody, senescence biology was investigated in prostate cancer (PCa) tissues |
25876105 | EXPERIMENTAL DESIGN: In vitro characterization of GLB1 was determined in primary prostate epithelial cell cultures passaged to replicative senescence and in therapy-induced senescence in PCa lines using chemotherapeutic agents |
25876105 | FFPE tissue microarrays were subjected to immunofluorescent staining for GLB1, Ki67 and HP1gamma and automated quantitative imaging initially using AQUA in exploratory samples and Vectra in a validation series |
25876105 | RESULTS: GLB1 expression accumulates in replicative and induced senescence and correlates with senescent morphology and P16 (CDKN2) expression |
25876105 | In tissue arrays, quantitative imaging detects increased GLB1 expression in high-grade prostatic intraepithelial neoplasia (HGPIN), known to contain senescent cells, and cancer compared to benign prostate tissues (p<0 |
25876105 | Within primary tumors, elevated GLB1 associates with lower T stage (p=0 |
25876105 | Increased GLB1 stratifies better PSA-free survival in intermediate grade PCa (0 |
25876105 | Tissues that elaborate higher GLB1 display increased uniformity of expression |
25876105 | CONCLUSION: Increased GLB1 is a valuable marker in formalin-fixed paraffin-embedded (FFPE) tissues for the senescence-like phenotype and associates with improved cancer outcomes |
23989658 | Combined treatment of MTOR inhibitor and radiation induce heterochromatin formation, an irreversible growth arrest and an increase of senescence-associated GLB1 (beta-galactosidase) activity, which appear to result from a constant activation of TP53 and a restoration in the activity of retinoblastoma 1 protein (RB1)-E2F1 |
22911222 | The increased expression of the senescence-related proteins Glb1, the cyclin-dependent kinase inhibitor p27(Kip1) and chromatin-regulating heterochromatin protein 1gamma (HP1gamma) were detected in LNCaP cells after AD in vitro by immunoblot and immunofluorescence microscopy |
22911222 | Immunohistochemical analysis of human prostate tumors removed after AD shows similar induction of Glb1, HP1gamma and decreased KI-67 |
21749859 | Our results show that GAPDH-depleted cells establish senescence phenotype, as revealed by proliferation arrest, changes in morphology, SA-beta-galactosidase staining, and more than 2-fold up-regulation of senescence-associated genes DEC1 and GLB1 |
16626397 | We demonstrate here that SA-beta-gal activity is expressed from GLB1, the gene encoding lysosomal beta-D-galactosidase, the activity of which is typically measured at acidic pH 4 |
16626397 | In addition, late passage normal fibroblasts expressing small-hairpin interfering RNA that depleted GLB1 mRNA underwent senescence but failed to express SA-beta-gal |
16626397 | GLB1 mRNA depletion also prevented expression of SA-beta-gal activity in HeLa cervical carcinoma cells induced to enter a senescent state by repression of their endogenous human papillomavirus E7 oncogene |
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