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Updated: Jan 25, 2026

Measuring Composition of CD95 Death-Inducing Signaling Complex and Processing of Procaspase-8 in this Complex
Published on: August 2, 2021
Modulation of CD95-mediated signaling by post-translational modifications: towards understanding CD95 signaling
1Translational Inflammation Research, Institute of Experimental Internal Medicine, Medical Faculty, Otto von Guericke University, Magdeburg, Germany.
Abstract:
CD95 is a member of the death receptor family and is well-known to promote apoptosis. However, accumulating evidence indicates that in some context CD95 has not only the potential to induce apoptosis but also can trigger non-apoptotic signal leading to cell survival, proliferation, cancer growth and metastasis. Despite extensive investigations focused on alterations in the expression level of CD95 and associated signal molecules, very few studies, however, have investigated the effects of post-translational modifications such as glycosylation, phosphorylation, palmitoylation, nitrosylation and glutathionylation on CD95 function. Post-translational modifications of CD95 in mammalian systems are likely to play a more prominent role than anticipated in CD95 induced cell death. In this review we will focus on the alterations in CD95-mediated signaling caused by post-translational modifications of CD95.
Insights
CD95 receptor can trigger apoptosis or cell survival signals. This review explores how post-translational modifications of CD95 impact its function in cell death and cancer.
Area of Science:
- Molecular Biology
- Cell Signaling
- Cancer Research
Background:
- CD95 (also known as Fas receptor) is a death receptor family member primarily known for inducing apoptosis.
- Emerging evidence shows CD95 can also promote non-apoptotic signals, contributing to cell survival, proliferation, and cancer progression.
- Research has largely focused on CD95 expression levels, with less attention paid to its post-translational modifications.
Purpose of the Study:
- To review the role of post-translational modifications (PTMs) in CD95-mediated signaling.
- To highlight how PTMs influence CD95's dual function in apoptosis and non-apoptotic pathways.
- To emphasize the significance of PTMs in CD95-induced cell death and cancer development.
Main Methods:
- Literature review focusing on studies investigating CD95 post-translational modifications.
- Analysis of alterations in CD95 signaling pathways due to PTMs like glycosylation, phosphorylation, and others.
- Synthesis of current knowledge on the impact of PTMs on CD95 function in mammalian systems.
Main Results:
- Post-translational modifications significantly alter CD95 signaling outcomes.
- PTMs can shift CD95 function from apoptosis induction to promoting cell survival and proliferation.
- These modifications are crucial for understanding CD95's complex roles in cell death and cancer biology.
Conclusions:
- Post-translational modifications play a critical, often underestimated, role in regulating CD95 function.
- Understanding CD95 PTMs is essential for deciphering its involvement in both cell death and cancer.
- Further research into CD95 PTMs could reveal novel therapeutic targets for cancer treatment.
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