CMTM6
Identifiers
Aliases	CMTM6, CKLFSF6, PRO2219, CKLF like MARVEL transmembrane domain containing 6, ayoube, gourari
External IDs	OMIM: 607889; MGI: 2447165; HomoloGene: 9845; GeneCards: CMTM6; OMA:CMTM6 - orthologs
Gene location (Human) Chr. Chromosome 3 (human)[1] Band 3p22.3 Start 32,481,312 bp[1] End 32,502,852 bp[1]
Gene location (Mouse) Chr. Chromosome 9 (mouse)[2] Band 9|9 F3 Start 114,560,184 bp[2] End 114,578,412 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in bronchial epithelial cell trabecular bone skin of thigh mucosa of paranasal sinus nipple mononuclear cell monocyte secondary oocyte lactiferous duct epithelium of nasopharynx Top expressed in granulocyte right kidney submandibular gland proximal tubule human kidney stroma of bone marrow Paneth cell external carotid artery blood jejunum More reference expression data BioGPS n/a
Gene ontology Molecular function cytokine activity protein binding Cellular component extracellular exosome membrane extracellular space plasma membrane integral component of membrane azurophil granule membrane specific granule membrane endosome early endosome membrane recycling endosome membrane Biological process chemotaxis neutrophil degranulation regulation of signaling receptor activity protein transport regulation of protein stability endocytic recycling Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 54918 67213 Ensembl ENSG00000091317 ENSMUSG00000032434 UniProt Q9NX76 Q9CZ69 RefSeq (mRNA) NM_017801 NM_026036 RefSeq (protein) NP_060271 NP_080312 Location (UCSC) Chr 3: 32.48 – 32.5 Mb Chr 9: 114.56 – 114.58 Mb PubMed search [3] [4]
Wikidata
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CKLF like MARVEL transmembrane domain-containing 6 (i.e. CMTM6), previously termed chemokine-like factor superfamily 6 (i.e. CKLFSF6), is a transmembrane protein encoded in humans by the CMTM6 gene (also termed the CKLFSF6, PRO2219, ayoube, or gourari gene). This gene is located in band 22.3 on the short (or "p") arm of chromosome 3.^[5] CMTM6 protein belongs to the CKLF-like MARVEL transmembrane domain-containing family of proteins.^[6] This family consist of 9 member proteins: CKLF and CMTM1 through CMTM8.^[7][8] The CMTM family proteins are involved in autoimmune diseases, cardiovascular diseases, the male reproductive system, haematopoiesis, and cancer development.^[8] CMTM6 protein regulates immune responses to normal and abnormal (particularly cancerous) cells.^[9][10]

Like the other members in the CMTM protein family, CMTM6 has a structure that contains domains (i.e. parts) similar to those in chemokine proteins; tetraspanin proteins (also termed transmembrane-4 superfamily proteins); the myelin and lymphocyte protein (also termed MAR protein); proteins that direct membrane vesicle trafficking; and proteins that are embedded across cell membranes. CMTM6 proteins are expressed in virtually all tissues^[11] and are located in cell plasma membranes (i.e. cell surface membranes), lysosomes, endosomes, cytosol, attached to the cell's cytoskeleton, and in extracellular spaces.^[8]

CMTM6 localizes with and binds to cell PD-L1 protein located on cell surface membranes thereby maintaining PD-L1'S expression at this site; it also localizes with PD-L1 protein located in recycling endosomes and thereby prevents PD-L1 from being degraded by lysosomal enzymes. These actions increase and maintain high levels of PD-L1 on cell surface membranes.^[11] PD-L1 protein on the surface of normal cells binds to PD-1 receptors on a type of cytotoxic T cells (i.e. CD8+ T cells^[11]) and thereby blocks these T-cells from organizing an immune response that would kill them. This PD-L1/CD8+ T cell circuit is one of several immune checkpoint mechanisms for maintaining self-tolerance, i.e. for preventing CD8+ T cells from attacking normal cells. Tumor cells may employ this immune-evading tactic: they may express PD-L1 and thereby block CD8+ T cell-mediated immune responses to themselves. In effect, the robust expression of PD-L1 helps not only normal cells but also cancer cells to evade immune destruction.^[12]

Various manufactured therapeutic monoclonal antibody drugs, e.g. pembrolizumab,^[12] atezolizumab, durvalumab^[13] nivolumab,^[14] and avelumab,^[9] bind to and inhibit the stimulation of PD-1 on CD8+ T cells by PD-L1. In effect, they block the ability of CMTMT6 to suppress PDL1/PD-1-stimulated CD8+ T-cell immune responses against tumor cells. One or more of these drugs are approved by the FDA for treating (as a single agent or in combination with adjuvant radiotherapy and/or chemotherapy) various cancers including certain types of Hodgkin's disease, melanomas, Merkel-cell carcinomas, cancers associated with microsatellite instability (e.g. certain types of colon, stomach, endometrial, ovarian, hepatobiliary tract, urinary tract, brain, and skin cancers), non-small cell lung cancer, head and neck cancers, esophageal cancers, bladder cancers, urinary track cancers, renal cell cancers, hepatocellular carcinomas,^[14] triple-negative breast cancers,^[15] undifferentiated pleomorphic sarcomas, and some forms of soft tissue sarcomas that have metastasized.^[16] A phase II study of 56 patients with cancer of unknown primary origin, i.e. a very common (2% to 5% of all diagnosed cancers) and difficult to treat metastatic cancer in which the primary cancer is unknown) found that nivolumab had a small (overall complete plus partial response rate of ~20%) beneficial effect.^[17] However, the use of any of these monoclonal antibody drugs as a single immunotherapy agent often benefits only a small percentage of cases with a particular disease, often lasts for only a short time, and may cause severe side-effects. Consequently, alternate methods of using these anti-PD-1 antibodies are being studied. Current preclinical studies and clinical trials are testing combinations of two anti-PD-1 antibodies or one anti-PD-1 antibody combined with an antibody that binds to and inhibits other immune response-regulating proteins, e.g. the CTLA4 protein (i.e. cytotoxic T-lymphocyte-associated protein 4), for their therapeutic effects in the just cited and other cancer types.^[18]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.