Browse C10orf54

Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
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 membrane Single-pass type I membrane protein
Domain PF07686 Immunoglobulin V-set domain
Function

Immunoregulatory receptor which inhibits the T-cell response (PubMed:24691993). May promote differentiation of embryonic stem cells, by inhibiting BMP4 signaling (By similarity). May stimulate MMP14-mediated MMP2 activation (PubMed:20666777).

> Gene Ontology
 
Biological Process -
Molecular Function -
Cellular Component -
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between C10orf54 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 C10orf54 and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
25964334Colon CarcinomaInhibit immunity (T cell function)A combinatorial blockade using monoclonal antibodies specific for VISTA and PD-L1 achieved optimal tumor-clearing therapeutic efficacy.
25267631MelanomaInhibit immunity (T cell function)Taken together, our data suggest that VISTA is a negative checkpoint regulator whose loss of function lowers the threshold for T-cell activation, allowing for an enhanced proinflammatory phenotype and an increase in the frequency and intensity of autoimmunity under susceptible conditions.
28346412Prostate CarcinomaInhibit immunityTo identify additional immune-inhibitory pathways in the prostate-tumor microenvironment, we evaluated untreated and ipilimumab-treated tumors from patients in a presurgical clinical trial. Levels of the PD-L1 and VISTA inhibitory molecules increased on independent subsets of macrophages in treated tumors. Our data suggest that VISTA represents another compensatory inhibitory pathway in prostate tumors after ipilimumab therapy.
24691994MelanomaInhibit immunity (T cell function)VISTA monoclonal antibody (mAb) treatment increased the number of tumor-specific T cells in the periphery and enhanced the infiltration, proliferation, and effector function of tumor-reactive T cells within the TME. VISTA blockade altered the suppressive feature of the TME by decreasing the presence of monocytic myeloid-derived suppressor cells and increasing the presence of activated dendritic cells within the tumor microenvironment. In addition, VISTA blockade impaired the suppressive function and reduced the emergence of tumor-specific Foxp3(+)CD4(+) regulatory T cells. Consequently, VISTA mAb administration as a monotherapy significantly suppressed the growth of both transplantable and inducible melanoma.
29771768Pancreatic CarcinomaInhibit immunityWe conclude that VISTA is predominantly expressed and up-regulated in the high-density infiltrated immune cells but minimal in human pancreatic cancerous cells. Our results for the first time highlight pancreatic immunosuppressive tumor microenvironment contributed by VISTA and its potential as a prominent target for pancreatic cancer immunotherapy.
29737375Cutaneous MelanomaInhibit immunityVISTA expression on tumor-infiltrating inflammatory cells in primary cutaneous melanoma correlates with poor disease-specific survival.
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
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 C10orf54 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
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
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 C10orf54 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.1240.739
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.3610.805
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)870.0490.964
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.2220.624
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.1320.947
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.6650.781
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.2930.552
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.4660.732
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.0260.987
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 481.0360.594
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 281.2430.668
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.30.0204
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of C10orf54 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) 277301.4-1.41
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 275901.7-1.71
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21174.817.6-12.80.307
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)8612.516.7-4.21
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)1311018.2-18.20.199
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
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of C10orf54. 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
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of C10orf54. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by C10orf54.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of C10orf54. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of C10orf54 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between C10orf54 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolC10orf54
Namechromosome 10 open reading frame 54
Aliases SISP1; GI24; B7H5; VISTA; stress induced secreted protein 1; V-domain Ig suppressor of T cell activation; DD ......
Chromosomal Location10q22.1
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting C10orf54 collected from DrugBank database.
> Drugs from DrugBank database
 

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