Browse ITGAM

Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
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 Cell membrane Single-pass type I membrane protein Membrane raft Single-pass type I membrane protein
Domain PF01839 FG-GAP repeat
PF00357 Integrin alpha cytoplasmic region
PF08441 Integrin alpha
PF00092 von Willebrand factor type A domain
Function

Integrin ITGAM/ITGB2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles. It is identical with CR-3, the receptor for the iC3b fragment of the third complement component. It probably recognizes the R-G-D peptide in C3b. Integrin ITGAM/ITGB2 is also a receptor for fibrinogen, factor X and ICAM1. It recognizes P1 and P2 peptides of fibrinogen gamma chain. Regulates neutrophil migration (PubMed:28807980). In association with beta subunit ITGB2/CD18, required for CD177-PRTN3-mediated activation of TNF primed neutrophils (PubMed:21193407). May regulate phagocytosis-induced apoptosis in extravasated neutrophils (By similarity). May play a role in mast cell development (By similarity).

> Gene Ontology
 
Biological Process GO:0002218 activation of innate immune response
GO:0002221 pattern recognition receptor signaling pathway
GO:0002224 toll-like receptor signaling pathway
GO:0002757 immune response-activating signal transduction
GO:0002758 innate immune response-activating signal transduction
GO:0002764 immune response-regulating signaling pathway
GO:0007229 integrin-mediated signaling pathway
GO:0007398 ectoderm development
GO:0010668 ectodermal cell differentiation
GO:0030198 extracellular matrix organization
GO:0031349 positive regulation of defense response
GO:0034142 toll-like receptor 4 signaling pathway
GO:0043062 extracellular structure organization
GO:0045088 regulation of innate immune response
GO:0045089 positive regulation of innate immune response
GO:0050900 leukocyte migration
Molecular Function GO:0001948 glycoprotein binding
GO:0046982 protein heterodimerization activity
Cellular Component GO:0008305 integrin complex
GO:0043235 receptor complex
GO:0098636 protein complex involved in cell adhesion
GO:0098802 plasma membrane receptor complex
> KEGG and Reactome Pathway
 
KEGG hsa04015 Rap1 signaling pathway
hsa04145 Phagosome
hsa04514 Cell adhesion molecules (CAMs)
hsa04610 Complement and coagulation cascades
hsa04640 Hematopoietic cell lineage
hsa04670 Leukocyte transendothelial migration
hsa04810 Regulation of actin cytoskeleton
Reactome R-HSA-202733: Cell surface interactions at the vascular wall
R-HSA-1280215: Cytokine Signaling in Immune system
R-HSA-1474244: Extracellular matrix organization
R-HSA-109582: Hemostasis
R-HSA-168256: Immune System
R-HSA-168249: Innate Immune System
R-HSA-216083: Integrin cell surface interactions
R-HSA-6785807: Interleukin-4 and 13 signaling
R-HSA-6798695: Neutrophil degranulation
R-HSA-449147: Signaling by Interleukins
R-HSA-166016: Toll Like Receptor 4 (TLR4) Cascade
R-HSA-168898: Toll-Like Receptors Cascades
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between ITGAM 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 ITGAM and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
19414774Lung carcinomaInhibit immunity (T cell function)A natural counterpart of CD11b(high)Ia(low) DCs was identified in tumor tissue, and CD11b(high)Ia(low) DCs sorted from 3LL lung cancer tissue expressed arginase I and inhibited T cell response.
23562161Colon CarcinomaInhibit immunityManipulations preventing tumor infiltration by CD11c(+)CD11b(+)Ly6C(hi) cells,?such as the local overexpression of ectonucleotidases, the blockade of purinergic receptors, or the neutralization of CD11b, abolished the immune?system-dependent antitumor activity of anthracyclines.
24965046GliomaInhibit immunityIntermittent metronomic cyclophosphamide scheduling strongly increased glioma-associated CD11b+ immune cells but not CD11b+Gr1+ myeloid-derived suppressor cells, while bone marrow and spleen reservoirs of the suppressor cells were decreased.
24907113melanomaInhibit immunityFurthermore, silencing COX-2 in murine 4T1 tumor cells reduced the accumulation of CD11b(+)Gr1(+) MDSCs in the spleen, resulting in concomitant improved in vivo clearance of NK-cell sensitive YAC-1 cells.
29636751colorectal carcinomaInhibit immunityMDSCs comprise a heterogeneous population of immature myeloid cells that can be distinct in two subtypes: CD11b+Ly6G+Ly6Clow with granulocytic phenotype (G-MDSCs) and CD11b+Ly6G-Ly6Chigh with monocytic phenotype (M-MDSCs).
29602801mesotheliomaInhibit immunityCharacterization of the whole blood at diagnosis identified similar, circulating, immunosuppressive CD11b+CD15+HLADR- granulocytes at increased frequency compared with healthy controls.
20042467Metastatic Malignant Neoplasm in the LiverInhibit immunity (T cell function)Liver CD11b(+)Gr1(+) cells are highly suppressive of T cell activation, proliferation, and cytotoxicity and induce the development of Tregs.
22955317Non-Small Cell Lung CarcinomaInhibit immunity (T cell function)Patients with NSCLC had a significantly higher ratio of CD11b(+)CD14(+) cells than healthy subjects, which was correlated with poor performance status and poor response to chemotherapy. Isolated CD11b(+)CD14(+) cells suppressed CD8(+) T-cell proliferation and IFN-γ production, and the former effect was attenuated by the inducible nitric oxide synthase (iNOS) inhibitor aminoguanidine hydrochloride, arginase inhibitor N-hydroxy-nor-l-arginine (nor-NOHA), and blocking antibodies for IL-4Rα(+) and IL-10.
20427766Ovarian CarcinomaPromote immunityHowever, we show that CD11b(+)Gr-1(+) cells found in ascites of epithelial ovarian cancer-bearing mice at advanced stages of disease are immunostimulatory rather than being immunosuppressive. Moreover, like dendritic cells, immunostimulatory CD11b(+)Gr-1(+) cells can strongly cross-prime, augmenting the proliferation of functional CTLs via signaling through the expression of costimulatory molecule CD80.
25183499melanomaInhibit immunityCD11b(+) myeloid cells from PLX4720-treated tumors also exhibited decreased immunosuppressive function on a per-cell basis.
25085111lung carcinomaInhibit immunityCD11b+MC were responsible for CD80 down-regulation on HBC and resulted in impaired T cell stimulation by HBC. CD80 loss on HBC was dependent on CD11b MC CD11b expression and STAT3 activity.
16849468lymphomaInhibit immunityHowever, CD11b(+) cells accumulated in primary ocular tumors and contained potent immunosuppressive activity when assayed in vitro. Thus, CD11b(+) cells that accumulate within the eye as tumors develop in the a.c. may contribute to immune evasion by primary ocular tumors by inhibiting CTLs within the eye
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
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 ITGAM 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
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
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 ITGAM in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.2990.346
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.2950.768
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.30.686
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-0.3910.443
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.7450.671
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.0620.979
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.2610.599
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.0980.941
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.6490.655
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 481.5130.215
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 282.3060.185
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.2640.141
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of ITGAM 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) 14177.111.8-4.71
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 1031033.3-23.30.423
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 41407.1-7.11
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 27737.42.74.70.294
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 27597.43.440.587
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21179.55.93.61
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)131115.49.16.31
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 91611.1011.10.36
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47250250.364
1329033130MelanomaallAnti-PD-1 (nivolumab) 38275.305.30.507
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22130001
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 161412.5012.50.485
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
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of ITGAM. 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
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of ITGAM. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by ITGAM.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of ITGAM. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of ITGAM expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between ITGAM and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolITGAM
Nameintegrin, alpha M (complement component 3 receptor 3 subunit)
Aliases CD11b; CR3A; integrin, alpha M (complement component receptor 3, alpha; also known as CD11b (p170), macropha ......
Chromosomal Location16p11.2
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting ITGAM collected from DrugBank database.
> Drugs from DrugBank database
 

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