Browse SNAI1

Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
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 Nucleus Cytoplasm. Note=Once phosphorylated (probably on Ser-107, Ser-111, Ser-115 and Ser-119) it is exported from the nucleus to the cytoplasm where subsequent phosphorylation of the destruction motif and ubiquitination involving BTRC occurs.
Domain -
Function

Involved in induction of the epithelial to mesenchymal transition (EMT), formation and maintenance of embryonic mesoderm, growth arrest, survival and cell migration. Binds to 3 E-boxes of the E-cadherin/CDH1 gene promoter and to the promoters of CLDN7 and KRT8 and, in association with histone demethylase KDM1A which it recruits to the promoters, causes a decrease in dimethylated H3K4 levels and represses transcription. During EMT, involved with LOXL2 in negatively regulating pericentromeric heterochromatin transcription (By similarity). SNAI1 recruits LOXL2 to pericentromeric regions to oxidize histone H3 and repress transcription which leads to release of heterochromatin component CBX5/HP1A, enabling chromatin reorganization and acquisition of mesenchymal traits (By similarity). Associates with EGR1 and SP1 to mediate tetradecanoyl phorbol acetate (TPA)-induced up-regulation of CDKN2B, possibly by binding to the CDKN2B promoter region 5'-TCACA-3. In addition, may also activate the CDKN2B promoter by itself.

> Gene Ontology
 
Biological Process GO:0001501 skeletal system development
GO:0001503 ossification
GO:0001649 osteoblast differentiation
GO:0001701 in utero embryonic development
GO:0001704 formation of primary germ layer
GO:0001707 mesoderm formation
GO:0001837 epithelial to mesenchymal transition
GO:0001890 placenta development
GO:0001892 embryonic placenta development
GO:0001942 hair follicle development
GO:0003002 regionalization
GO:0003007 heart morphogenesis
GO:0003197 endocardial cushion development
GO:0003198 epithelial to mesenchymal transition involved in endocardial cushion formation
GO:0003203 endocardial cushion morphogenesis
GO:0003272 endocardial cushion formation
GO:0006694 steroid biosynthetic process
GO:0006766 vitamin metabolic process
GO:0006775 fat-soluble vitamin metabolic process
GO:0007043 cell-cell junction assembly
GO:0007219 Notch signaling pathway
GO:0007369 gastrulation
GO:0007389 pattern specification process
GO:0007498 mesoderm development
GO:0007507 heart development
GO:0008202 steroid metabolic process
GO:0008544 epidermis development
GO:0008630 intrinsic apoptotic signaling pathway in response to DNA damage
GO:0009110 vitamin biosynthetic process
GO:0010717 regulation of epithelial to mesenchymal transition
GO:0010718 positive regulation of epithelial to mesenchymal transition
GO:0010894 negative regulation of steroid biosynthetic process
GO:0010957 negative regulation of vitamin D biosynthetic process
GO:0019216 regulation of lipid metabolic process
GO:0019218 regulation of steroid metabolic process
GO:0022404 molting cycle process
GO:0022405 hair cycle process
GO:0030330 DNA damage response, signal transduction by p53 class mediator
GO:0030335 positive regulation of cell migration
GO:0030656 regulation of vitamin metabolic process
GO:0031069 hair follicle morphogenesis
GO:0034329 cell junction assembly
GO:0034330 cell junction organization
GO:0040017 positive regulation of locomotion
GO:0042303 molting cycle
GO:0042359 vitamin D metabolic process
GO:0042362 fat-soluble vitamin biosynthetic process
GO:0042368 vitamin D biosynthetic process
GO:0042633 hair cycle
GO:0042770 signal transduction in response to DNA damage
GO:0043297 apical junction assembly
GO:0043516 regulation of DNA damage response, signal transduction by p53 class mediator
GO:0043518 negative regulation of DNA damage response, signal transduction by p53 class mediator
GO:0043588 skin development
GO:0044283 small molecule biosynthetic process
GO:0045216 cell-cell junction organization
GO:0045833 negative regulation of lipid metabolic process
GO:0045939 negative regulation of steroid metabolic process
GO:0045992 negative regulation of embryonic development
GO:0045995 regulation of embryonic development
GO:0046137 negative regulation of vitamin metabolic process
GO:0046890 regulation of lipid biosynthetic process
GO:0048332 mesoderm morphogenesis
GO:0048568 embryonic organ development
GO:0048608 reproductive structure development
GO:0048730 epidermis morphogenesis
GO:0048762 mesenchymal cell differentiation
GO:0050810 regulation of steroid biosynthetic process
GO:0051055 negative regulation of lipid biosynthetic process
GO:0051216 cartilage development
GO:0051272 positive regulation of cellular component movement
GO:0060021 palate development
GO:0060317 cardiac epithelial to mesenchymal transition
GO:0060485 mesenchyme development
GO:0060536 cartilage morphogenesis
GO:0060556 regulation of vitamin D biosynthetic process
GO:0060706 cell differentiation involved in embryonic placenta development
GO:0060707 trophoblast giant cell differentiation
GO:0060800 regulation of cell differentiation involved in embryonic placenta development
GO:0060806 negative regulation of cell differentiation involved in embryonic placenta development
GO:0060972 left/right pattern formation
GO:0061311 cell surface receptor signaling pathway involved in heart development
GO:0061314 Notch signaling involved in heart development
GO:0061448 connective tissue development
GO:0061458 reproductive system development
GO:0070830 bicellular tight junction assembly
GO:0072132 mesenchyme morphogenesis
GO:0072331 signal transduction by p53 class mediator
GO:0097193 intrinsic apoptotic signaling pathway
GO:0098773 skin epidermis development
GO:1901615 organic hydroxy compound metabolic process
GO:1901617 organic hydroxy compound biosynthetic process
GO:1901796 regulation of signal transduction by p53 class mediator
GO:1901797 negative regulation of signal transduction by p53 class mediator
GO:1901888 regulation of cell junction assembly
GO:1902229 regulation of intrinsic apoptotic signaling pathway in response to DNA damage
GO:1902230 negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage
GO:1902532 negative regulation of intracellular signal transduction
GO:2000147 positive regulation of cell motility
GO:2000241 regulation of reproductive process
GO:2000242 negative regulation of reproductive process
GO:2000810 regulation of bicellular tight junction assembly
GO:2001020 regulation of response to DNA damage stimulus
GO:2001021 negative regulation of response to DNA damage stimulus
GO:2001233 regulation of apoptotic signaling pathway
GO:2001234 negative regulation of apoptotic signaling pathway
GO:2001242 regulation of intrinsic apoptotic signaling pathway
GO:2001243 negative regulation of intrinsic apoptotic signaling pathway
Molecular Function GO:0000982 transcription factor activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0001078 transcriptional repressor activity, RNA polymerase II core promoter proximal region sequence-specific binding
GO:0001227 transcriptional repressor activity, RNA polymerase II transcription regulatory region sequence-specific binding
Cellular Component -
> KEGG and Reactome Pathway
 
KEGG hsa04520 Adherens junction
Reactome -
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between SNAI1 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 SNAI1 and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
28574228CholangiocarcinomaInhibit immunityOur findings further indicated that CCA cells with EMT-like features appear to generate immunosuppressive natural T regulatory-like cluster of differentiation 4-positive (CD4+)CD25-cells rather than to increase CD4+CD25+natural T regulatory cells, in part by mediating T regulatory-inducible cytokines such as transforming growth factor β1 and interleukin 2.These results demonstrate that aPKC-ι promotes EMT and induces immunosuppression through the aPKC-ι/P-Sp1/Snail signaling pathway and may be a potential therapeutic target for CCA.
23509364Colorectal CarcinomaPromote immunityNK group 2, member D (NKG2D) is an NK cell-activating receptor crucially involved in cancer immunosurveillance. In this study, we show that induction of EMT by TGF-β stimulation of human keratinocytes, by glycogen synthase kinase-3β inhibition in several epithelial tumor cell lines, and by Snail1 overexpression in colorectal cancer cells strongly upregulated the expression of NKG2D ligands (NKG2DLs), MHC class I chain-related molecules A and B (MICA/B) and ULBP1-3.
29632713breast carcinomaInhibit immunityThe phagocytosis of EMT-activated cells was rescued by using CD47 blocking antibody or by genetic targeting of SNAI1, ZEB1 or CD47.
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
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 SNAI1 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
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
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 SNAI1 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.7470.172
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-1.3330.266
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.3230.749
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-1.010.0321
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.9610.399
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-1.0630.487
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.0510.924
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.1790.836
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.4740.575
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 481.1450.26
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 282.3670.0673
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.4210.009
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of SNAI1 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) 27730001
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27590001
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) 91606.2-6.21
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59011.1-11.11
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
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of SNAI1. 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
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of SNAI1. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by SNAI1.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of SNAI1. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of SNAI1 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between SNAI1 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolSNAI1
Namesnail family zinc finger 1
Aliases SNA; SLUGH2; SNAH; SNAIL1; SNAIL; snail 1 (drosophila homolog), zinc finger protein; snail homolog 1 (Drosop ......
Chromosomal Location20q13.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting SNAI1 collected from DrugBank database.
> Drugs from DrugBank database
 

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