Target intelligence / Profile preview

COP9 signalosome subunit 6 (COPS6)

Target
COPS6
Molecular classification
Signalosome subunit, Translation initiation factor 3 (eIF3) superfamily member, Protein complex component, Ubiquitin-proteasome pathway regulator, Other
01

Overview

COP9 signalosome subunit 6 (COPS6) is one of eight subunits of the COP9 signalosome (CSN), a highly conserved multi-protein complex that is structurally and functionally similar to the 19S regulatory particle of the 26S proteasome[1][3]. COPS6 participates as an essential regulator in multiple signal transduction pathways, primarily through modulation and positive regulation of SCF-type E3 ubiquitin ligases, resulting in control of protein degradation via the ubiquitin-proteasome system[1][3][4]. It is also involved in cell cycle regulation, DNA damage response, immune cell infiltration, and transcriptional control[1][2][3]. COPS6 has been implicated as a crucial factor in the progression and prognosis of numerous cancers, correlating with poor outcomes and high-risk molecular profiles[2]. Its overexpression is associated with enhanced tumor growth, invasion, metastasis, and immune evasion, and it has interactions with key pathways such as p53-mediated tumor suppression, PD-L1 stability, and epithelial-mesenchymal transition[2]. There is growing interest in COPS6 as a pan-cancer biomarker, although clinical interventions directly targeting COPS6 have not reached advanced development[2][3].

Other names
COP9 signalosome complex subunit 6COPS6CSN6HVIPSGN6hVIPMOV34-34KDJAB1-containing signalosome subunit 6MOV34 homologVpr-interacting proteinCOP9 subunit 6 (MOV34 homolog, 34 kD)COP9 constitutive photomorphogenic homolog subunit 6
02

Mechanism of action

Drug mechanism is not established—however, modulation of COPS6 would be expected to affect processes such as ubiquitin-mediated proteolysis, signal transduction, and immune checkpoint pathways in cancer

03

Biological functions

Regulation of signal transductionCell cycle controlProtein degradation via ubiquitin-proteasome pathwayRegulation of E3 ubiquitin ligasesDNA damage responseTranscriptional regulationImmune modulation (HIV-1 cofactor, tumor immune evasion)Apoptosis
04

Disease associations

Cancer (colorectal, breast, prostate, cervical, melanoma, and others)Xeroderma Pigmentosum, Complementation Group EOther potential roles in neurodegenerative disease (Parkinson's disease, inferred from pathway enrichment)
05

Safety considerations

Potential for broad effects on protein degradation pathways, impacting cell viability and homeostasisPossible immunosuppression and interference with DNA repair mechanismsOff-target effects due to regulation of multiple signaling pathways
06

Biomarkers

High COPS6 expression serves as a prognostic biomarker for multiple cancers (including breast, colorectal, hepatocellular, and renal cancers)Associated with tumor mutational burden, microsatellite instability, immune infiltration profiles

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