Target intelligence / Profile preview

Fas receptor (also known as CD95 or APO-1) (CD95 (Fas))

Target
CD95 (Fas)
Molecular classification
Receptor, Tumor necrosis factor receptor (TNF receptor) superfamily, Death receptor
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Overview

The Fas receptor (CD95, APO-1, TNFRSF6) is a type I transmembrane protein and prototypical member of the tumor necrosis factor receptor superfamily, characterized by an intracellular death domain essential for triggering apoptosis upon binding of Fas ligand (FasL/CD95L). The CD95/Fas system is central to immune homeostasis, enabling deletion of activated or autoreactive lymphocytes and contributing to cytotoxic lymphocyte-mediated killing of cancer or infected cells, while also involved in the shutdown of immune responses after pathogen clearance. In the immune system, disruption of Fas-mediated cell death leads to uncontrolled lymphoproliferation and autoimmunity, while in cancer, evasion of Fas-induced apoptosis permits tumor cell survival. Beyond apoptosis, Fas can trigger non-apoptotic signaling cascades (such as via NF-κB), regulating inflammation, cell proliferation, and survival. Therapeutic targeting of the Fas pathway is being investigated for cancer, autoimmune, and inflammatory disorders, but is challenged by ubiquitous expression and potential for widespread tissue toxicity.

Other names
FasCD95APO-1TNFRSF6 (tumor necrosis factor receptor superfamily member 6)
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Mechanism of action

Induction of apoptosis via death-inducing signaling complex (DISC) formation, activating caspase-8\nNon-apoptotic immune modulation (NF-κB signaling, cell survival/proliferation pathways)

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Biological functions

Apoptosis (programmed cell death)Immune responseImmune cell homeostasisNegative regulation of immune cell survivalNon-apoptotic signaling (e.g., NF-κB activation)
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Disease associations

CancerAutoimmune diseaseChronic inflammationInfection
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Safety considerations

Risk of excessive immunosuppression (autoimmunity or immune deficiency)Liver toxicity and hepatocyte apoptosisOff-target tissue damage due to widespread Fas expression
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Interacting drugs

Concizumab (experimental, anti-FasL antibodies or decoy receptors)

2 more in the full profile.

07

Biomarkers

Fas (CD95) expression on lymphocytes/tumor cellsFas ligand (FasL) levels in serum or tissues

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