CXCL9
Identifiers
Aliases	CXCL9, CMK, Humig, MIG, SCYB9, crg-10, C-X-C motif chemokine ligand 9
External IDs	OMIM: 601704; MGI: 1352449; HomoloGene: 1813; GeneCards: CXCL9; OMA:CXCL9 - orthologs
Gene location (Human) Chr. Chromosome 4 (human)[1] Band 4q21.1 Start 76,001,275 bp[1] End 76,007,509 bp[1]
Gene location (Mouse) Chr. Chromosome 5 (mouse)[2] Band 5 E2|5 46.51 cM Start 92,469,206 bp[2] End 92,475,938 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in appendix lymph node epithelium of nasopharynx superficial temporal artery rectum olfactory zone of nasal mucosa palpebral conjunctiva testicle gallbladder parietal pleura Top expressed in subcutaneous adipose tissue mesenteric lymph nodes submandibular gland white adipose tissue spleen left lobe of liver tunica adventitia of aorta brown adipose tissue jejunum mammary gland More reference expression data BioGPS More reference expression data
Gene ontology Molecular function cytokine activity CXCR3 chemokine receptor binding chemokine activity protein binding Cellular component extracellular region external side of plasma membrane extracellular space intracellular anatomical structure Biological process G protein-coupled receptor signaling pathway chemokine-mediated signaling pathway cell-cell signaling positive regulation of release of sequestered calcium ion into cytosol positive regulation of cAMP-mediated signaling chemotaxis positive regulation of leukocyte chemotaxis cellular defense response positive regulation of myoblast fusion response to lipopolysaccharide regulation of cell population proliferation positive regulation of myoblast differentiation defense response to virus immune response signal transduction defense response inflammatory response T cell chemotaxis antimicrobial humoral immune response mediated by antimicrobial peptide regulation of signaling receptor activity adenylate cyclase-activating G protein-coupled receptor signaling pathway response to bacterium neutrophil chemotaxis leukocyte chemotaxis cellular response to lipopolysaccharide Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 4283 17329 Ensembl ENSG00000138755 ENSMUSG00000029417 UniProt Q07325 P18340 RefSeq (mRNA) NM_002416 NM_008599 RefSeq (protein) NP_002407 NP_032625 Location (UCSC) Chr 4: 76 – 76.01 Mb Chr 5: 92.47 – 92.48 Mb PubMed search [3] [4]
Wikidata
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Chemokine (C-X-C motif) ligand 9 (CXCL9) is a small cytokine belonging to the CXC chemokine family that is also known as monokine induced by gamma interferon (MIG). The CXCL9 is one of the chemokine which plays role to induce chemotaxis, promote differentiation and multiplication of leukocytes, and cause tissue extravasation.^[5]

The CXCL9/CXCR3 receptor regulates immune cell migration, differentiation, and activation. Immune reactivity occurs through recruitment of immune cells, such as cytotoxic lymphocytes (CTLs), natural killer (NK) cells, NKT cells, and macrophages. Th1 polarization also activates the immune cells in response to IFN-γ.^[6] Tumor-infiltrating lymphocytes are a key for clinical outcomes and prediction of the response to checkpoint inhibitors.^[7] In vivo studies suggest the axis plays a tumorigenic role by increasing tumor proliferation and metastasis.^{[citation needed]} CXCL9 predominantly mediates lymphocytic infiltration to the focal sites and suppresses tumor growth.^[8]

It is closely related to two other CXC chemokines called CXCL10 and CXCL11, whose genes are located near the gene for CXCL9 on human chromosome 4.^[9][10] CXCL9, CXCL10 and CXCL11 all elicit their chemotactic functions by interacting with the chemokine receptor CXCR3.^[11]

CXCL9, -10, -11 have proven to be valid biomarkers for the development of heart failure and left ventricular dysfunction, suggesting an underlining pathophysiological relation between levels of these chemokines and the development of adverse cardiac remodeling.^[12][13]

This chemokine has also been associated as a biomarker for diagnosing Q fever infections.^[14]

CXCL9 has been shown to interact with CXCR3.^[15][16]

For immune cell differentiation, some reports show that CXCL9 lead to Th1 polarization through CXCR3.^[17] In vivo model by Zohar et al. showed that CXCL9, drove increased transcription of T-bet and RORγ, leading to the polarization of Foxp3⁻ type 1 regulatory (Tr1) cells or T helper 17 (Th17) from naive T cells via STAT1, STAT4, and STAT5 phosphorylation.^[17]

Several studies have shown that tumor-associated macrophages (TAMs) play modulatory activities in the TME, and the CXCL9/CXCR3 axis impacts TAMs polarization. The TAMs have opposite effects; M1 for anti-tumor activities, and M2 for pro-tumor activities. Oghumu et al. clarified that CXCR3 deficient mice displayed increased IL-4 production and M2 polarization in a murine breast cancer model, and decreased innate and immune cell-mediated anti-tumor responses.^[18]

For immune cell activation, CXCL9 stimulate immune cells through Th1 polarization and activation. Th1 cells produce IFN-γ, TNF-α, IL-2 and enhance anti-tumor immunity by stimulating CTLs, NK cells and macrophages.^[19] The IFN-γ-dependent immune activation loop also promotes CXCL9 release.^[5]

Immune cells, like Th1, CTLs, NK cells, and NKT cells, show anti-tumor effect against cancer cells through paracrine CXCL9/CXCR3 in tumor models.^[8] The autocrine CXCL9/CXCR3 signaling in cancer cells increases cancer cell proliferation, angiogenesis, and metastasis.^{[citation needed]}

The relationship between CXCL9/CXCR3 and the PDL-1/PD-1 is an important area of research. Programmed cell death-1 (PD-1) shows increased expression on T cells at the tumor site compared to T cells present in the peripheral blood, and anti-PD-1 therapy can inhibit “immune escape” and the immune activation.^[20] Peng et al. showed that anti-PD-1 could not only enhance T cell-mediated tumor regression but also increase the expression of IFN-γ but not CXCL9 by bone marrow–derived cells.^[20] Blockade of the PDL-1/PD-1 axis in T cells may trigger a positive feedback loop at the tumor site through the CXCL9/CXCR3 axis. Also using anti-CTLA4 antibody, this axis was significantly up-regulated in pretreatment melanoma lesions in patients with good clinical response after ipilimumab administration.^[21]

CXCL9 has also been identified as candidate biomarker of adoptive T cell transfer therapy in metastatic melanoma.^[22] The role of CXCL9/CXCR3 in TME and immune response - this plays a critical role in immune activation through paracrine signaling, impacting efficacy of cancer treatments.^[5]

• Human CXCL9 genome location and CXCL9 gene details page in the UCSC Genome Browser.