Browse SDCBP

Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Basic function annotation.
> Subcellular Location, Domain and Function
> Gene Ontology
> KEGG and Reactome Pathway
> Subcellular Location, Domain and Function
 
Subcellular Location Cell junction, focal adhesion Cell junction, adherens junction Cell membrane Peripheral membrane protein Endoplasmic reticulum membrane Peripheral membrane protein Nucleus Melanosome Cytoplasm, cytosol Cytoplasm, cytoskeleton Secreted, exosome Membrane raft Note=Mainly membrane-associated. Localized to adherens junctions, focal adhesions and endoplasmic reticulum. Colocalized with actin stress fibers. Also found in the nucleus. Identified by mass spectrometry in melanosome fractions from stage I to stage IV. Associated to the plasma membrane in the presence of FZD7 and phosphatidylinositol 4,5-bisphosphate (PIP2) (PubMed:27386966).
Domain PF00595 PDZ domain (Also known as DHR or GLGF)
Function

Multifunctional adapter protein involved in diverse array of functions including trafficking of transmembrane proteins, neuro and immunomodulation, exosome biogenesis, and tumorigenesis (PubMed:26291527). Positively regulates TGFB1-mediated SMAD2/3 activation and TGFB1-induced epithelial-to-mesenchymal transition (EMT) and cell migration in various cell types. May increase TGFB1 signaling by enhancing cell-surface expression of TGFR1 by preventing the interaction between TGFR1 and CAV1 and subsequent CAV1-dependent internalization and degradation of TGFR1 (PubMed:25893292). In concert with SDC1/4 and PDCD6IP, regulates exosome biogenesis (PubMed:22660413). Regulates migration, growth, proliferation, and cell cycle progression in a variety of cancer types (PubMed:26539120). In adherens junctions may function to couple syndecans to cytoskeletal proteins or signaling components. Seems to couple transcription factor SOX4 to the IL-5 receptor (IL5RA) (PubMed:11498591). May also play a role in vesicular trafficking (PubMed:11179419). Seems to be required for the targeting of TGFA to the cell surface in the early secretory pathway (PubMed:10230395).

> Gene Ontology
 
Biological Process GO:0001558 regulation of cell growth
GO:0001837 epithelial to mesenchymal transition
GO:0002090 regulation of receptor internalization
GO:0002091 negative regulation of receptor internalization
GO:0006612 protein targeting to membrane
GO:0006887 exocytosis
GO:0006898 receptor-mediated endocytosis
GO:0006929 substrate-dependent cell migration
GO:0006930 substrate-dependent cell migration, cell extension
GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
GO:0007179 transforming growth factor beta receptor signaling pathway
GO:0007254 JNK cascade
GO:0007265 Ras protein signal transduction
GO:0007346 regulation of mitotic cell cycle
GO:0009894 regulation of catabolic process
GO:0009895 negative regulation of catabolic process
GO:0010498 proteasomal protein catabolic process
GO:0010717 regulation of epithelial to mesenchymal transition
GO:0010718 positive regulation of epithelial to mesenchymal transition
GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
GO:0016049 cell growth
GO:0016050 vesicle organization
GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
GO:0017157 regulation of exocytosis
GO:0030031 cell projection assembly
GO:0030100 regulation of endocytosis
GO:0030307 positive regulation of cell growth
GO:0030335 positive regulation of cell migration
GO:0030511 positive regulation of transforming growth factor beta receptor signaling pathway
GO:0031098 stress-activated protein kinase signaling cascade
GO:0031329 regulation of cellular catabolic process
GO:0031330 negative regulation of cellular catabolic process
GO:0031623 receptor internalization
GO:0032434 regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0032435 negative regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0032872 regulation of stress-activated MAPK cascade
GO:0032874 positive regulation of stress-activated MAPK cascade
GO:0040017 positive regulation of locomotion
GO:0042176 regulation of protein catabolic process
GO:0042177 negative regulation of protein catabolic process
GO:0043112 receptor metabolic process
GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process
GO:0043410 positive regulation of MAPK cascade
GO:0044089 positive regulation of cellular component biogenesis
GO:0045806 negative regulation of endocytosis
GO:0045861 negative regulation of proteolysis
GO:0045921 positive regulation of exocytosis
GO:0045927 positive regulation of growth
GO:0046328 regulation of JNK cascade
GO:0046330 positive regulation of JNK cascade
GO:0048013 ephrin receptor signaling pathway
GO:0048259 regulation of receptor-mediated endocytosis
GO:0048261 negative regulation of receptor-mediated endocytosis
GO:0048762 mesenchymal cell differentiation
GO:0051047 positive regulation of secretion
GO:0051051 negative regulation of transport
GO:0051272 positive regulation of cellular component movement
GO:0051403 stress-activated MAPK cascade
GO:0060389 pathway-restricted SMAD protein phosphorylation
GO:0060393 regulation of pathway-restricted SMAD protein phosphorylation
GO:0060485 mesenchyme development
GO:0060627 regulation of vesicle-mediated transport
GO:0061136 regulation of proteasomal protein catabolic process
GO:0070302 regulation of stress-activated protein kinase signaling cascade
GO:0070304 positive regulation of stress-activated protein kinase signaling cascade
GO:0071559 response to transforming growth factor beta
GO:0071560 cellular response to transforming growth factor beta stimulus
GO:0071971 extracellular exosome assembly
GO:0072657 protein localization to membrane
GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
GO:0090100 positive regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
GO:0090150 establishment of protein localization to membrane
GO:0090287 regulation of cellular response to growth factor stimulus
GO:1901799 negative regulation of proteasomal protein catabolic process
GO:1902115 regulation of organelle assembly
GO:1902117 positive regulation of organelle assembly
GO:1903050 regulation of proteolysis involved in cellular protein catabolic process
GO:1903051 negative regulation of proteolysis involved in cellular protein catabolic process
GO:1903362 regulation of cellular protein catabolic process
GO:1903363 negative regulation of cellular protein catabolic process
GO:1903532 positive regulation of secretion by cell
GO:1903541 regulation of exosomal secretion
GO:1903543 positive regulation of exosomal secretion
GO:1903551 regulation of extracellular exosome assembly
GO:1903553 positive regulation of extracellular exosome assembly
GO:1903844 regulation of cellular response to transforming growth factor beta stimulus
GO:1903846 positive regulation of cellular response to transforming growth factor beta stimulus
GO:1990182 exosomal secretion
GO:2000147 positive regulation of cell motility
Molecular Function GO:0001664 G-protein coupled receptor binding
GO:0001948 glycoprotein binding
GO:0005109 frizzled binding
GO:0005126 cytokine receptor binding
GO:0005137 interleukin-5 receptor binding
GO:0008022 protein C-terminus binding
GO:0008093 cytoskeletal adaptor activity
GO:0019838 growth factor binding
GO:0030674 protein binding, bridging
GO:0042043 neurexin family protein binding
GO:0045296 cadherin binding
GO:0045545 syndecan binding
GO:0046875 ephrin receptor binding
GO:0046982 protein heterodimerization activity
GO:0047485 protein N-terminus binding
GO:0050839 cell adhesion molecule binding
GO:0060090 binding, bridging
GO:0070851 growth factor receptor binding
GO:0098631 protein binding involved in cell adhesion
GO:0098632 protein binding involved in cell-cell adhesion
GO:0098641 cadherin binding involved in cell-cell adhesion
Cellular Component GO:0005895 interleukin-5 receptor complex
GO:0005913 cell-cell adherens junction
GO:0005924 cell-substrate adherens junction
GO:0005925 focal adhesion
GO:0030055 cell-substrate junction
GO:0042470 melanosome
GO:0043235 receptor complex
GO:0045121 membrane raft
GO:0048770 pigment granule
GO:0072562 blood microparticle
GO:0098589 membrane region
GO:0098802 plasma membrane receptor complex
GO:0098857 membrane microdomain
> KEGG and Reactome Pathway
 
KEGG -
Reactome R-HSA-422475: Axon guidance
R-HSA-1266738: Developmental Biology
R-HSA-2682334: EPH-Ephrin signaling
R-HSA-3928664: Ephrin signaling
R-HSA-168256: Immune System
R-HSA-168249: Innate Immune System
R-HSA-373760: L1CAM interactions
R-HSA-447043: Neurofascin interactions
R-HSA-6798695: Neutrophil degranulation
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between SDCBP and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells.
> Text Mining
 
  Literatures describing the relation between SDCBP and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
29845474Triple-Negative Breast CarcinomaInhibit immunitySyntenin1/MDA-9 (SDCBP) induces immune evasion in triple-negative breast cancer by upregulating PD-L1. Western blot and flow cytometry analyses demonstrated that syntenin1 induced CD8+ T cell apoptosis in vitro and in vivo through upregulating PD-L1.
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets.
> High-throughput Screening
  Statistical results of SDCBP in screening data sets for detecting immune reponses.
PMID Screening System Cancer Type Cell Line Data Set Statistical Results Relation to immunity
29301958CRISPR-Cas9 melanomaB16F10Pmel-1 T cell NA/NSNA/NS
29301958CRISPR-Cas9 melanomaB16F10OT-1 T cell NA/NSNA/NS
28783722CRISPR-Cas9 melanomaMel6242CT-CRISPR NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX+Anti-PD1 NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX NA/NSNA/NS
25691366RNAiBreast cancerMCF7Luc-CTL assay NA/NSNA/NS
24476824shRNAmelanomaB16Primary screen NA/NSNA/NS
24476824shRNAmelanomaB16Secondary screen NA/NSNA/NS
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets.
> Expression difference between responders and non-responders
> Mutation difference between responders and non-responders
> Expression difference between responders and non-responders
 
Points in the above scatter plot represent the expression difference of SDCBP in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.0760.863
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.1150.977
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.0410.988
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.1730.696
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.7320.687
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.5320.814
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.3730.54
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.7270.792
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.1020.975
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.7230.736
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 281.1850.729
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 682300.0750.37
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of SDCBP in various data sets.
No PMID Cancer type Group Drug # Res # NRes % Mut/Res % Mut/NRes % Diff (R vs NR) Pval Anno
125765070Non-small cell lung cancer (NSCLC)allAnti-PD-1 (pembrolizumab) 14170001
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 1030001
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 4140001
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 27737.407.40.0709
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27597.407.40.096
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)211705.9-5.90.447
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)131109.1-9.10.458
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38270001
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22130001
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 16140001
1629301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 11130001
1729301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 610001
1829301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 5120001
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of SDCBP. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene.
> Lymphocyte
 
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of SDCBP. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by SDCBP.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of SDCBP. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of SDCBP expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between SDCBP and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolSDCBP
Namesyndecan binding protein (syntenin)
Aliases SYCL; MDA-9; MDA9; ST1; TACIP18; melanoma differentiation associated protein-9; melanoma differentiation-ass ......
Chromosomal Location8q12.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting SDCBP collected from DrugBank database.
> Drugs from DrugBank database
 

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