Results 21 to 30 of about 3,939 (188)

IRE1 RNase controls CD95-mediated cell death [PDF]

open access: yesEMBO Reports
Signalling by the Unfolded Protein Response (UPR) or by the Death Receptors (DR) are frequently activated towards pro-tumoral outputs in cancer. Herein, we demonstrate that the UPR sensor IRE1 controls the expression of the DR CD95/Fas, and its cell ...
Diana Pelizzari-Raymundo   +11 more
doaj   +2 more sources

Oligomerised RIPK1 is the main core component of the CD95 necrosome [PDF]

open access: yesThe EMBO Journal
The necrosome is the key macromolecular signaling platform initiating necroptosis, i.e., a RIPK1/RIPK3-dependent program of cell death with an important role in the control of inflammation in multicellular organisms.
Nikita V Ivanisenko   +8 more
doaj   +2 more sources

Cell Apoptosis and Glucocorticoid‐Induced Osteonecrosis

open access: yesMed Research
Glucocorticoids (GCs) are steroid hormones commonly used to treat inflammation, autoimmune diseases, and malignant tumors. By inhibiting bone formation and promoting osteoclast apoptosis, GCs significantly accelerate the onset of femoral head ...
Xiumei Tang   +7 more
doaj   +2 more sources

Method to Measure Sphingomyelin Synthase Activity Changes in Response to CD95L

open access: yes, 2017
Sphingomyelin synthases 1 and 2 convert the anti-oncometabolite ceramide to sphingomyelin, the most abundant sphingolipid in plasma membrane. CD95L-induced ceramide increase is associated with the caspase-dependent inhibition of sphingomyelin synthesis, which enhances the mitochondrial route to apoptosis.
Bilal, Fatima   +6 more
openaire   +4 more sources

The CD95/CD95L signaling pathway: A role in carcinogenesis [PDF]

open access: yesBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2014
Apoptosis is a fundamental process that contributes to tissue homeostasis, immune responses, and development. The receptor CD95, also called Fas, is a member of the tumor necrosis factor receptor (TNF-R) superfamily. Its cognate ligand, CD95L, is implicated in immune homeostasis and immune surveillance, and various lineages of malignant cells exhibit ...
Fouqué, Amélie   +2 more
openaire   +6 more sources

The Association of Programmed Death Ligand 1 (PD-L1) and Cluster of Differentiation 95 Ligand (CD95L) Immunoexpression with Chemotherapy Response in Classical Hodgkin Lymphoma

open access: yesIndonesian Journal of Cancer, 2022
Background: Programmed Death Ligand (PD-L1) and Cluster of Differentiation 95 (CD95L) are influenced by oncogenes and function in the anti-apoptosis process which is thought to play a role in chemotherapy resistance.
Hasrayati Agustina   +2 more
doaj   +1 more source

Blockade of CD95/CD95L death signaling enhances CAR T cell persistence and antitumor efficacy [PDF]

open access: yes, 2021
Despite the encouraging outcome of anti-CD19 chimeric antigen receptor T (CAR T) cell therapy in patients with B cell malignancies, CAR T cell persistence remains a major clinical challenge.
He, Bailin
core   +1 more source

Involvement of CD95 and ligand in CD4+ T-cell and CD8+ T-cell depletion and hepatic cytolysis in patients with chronic viral hepatitis B

open access: yesAfrican Journal of Laboratory Medicine, 2021
Background: Chronic viral hepatitis B (HBV) is characterised by progressive hepatocyte destruction and T-cell depletion. The mechanisms of the CD95-CD95 ligand (CD95L) signalling pathway during this chronic disease and the cirrhotic process remains ...
Franklin S. Azebaze Agueguia   +8 more
doaj   +1 more source

The influence of CD95L expression on tumor rejection in mice [PDF]

open access: yesEuropean Journal of Immunology, 2003
AbstractMany tumors express the death ligand CD95L (CD178, APO‐1L, FasL) and can kill activated T cells in vitro. This may enable the tumor cells to suppress anti‐tumor immune responses, a phenomenon called "tumor counterattack". Preliminary evidence of tumor counterattack in human tumors exists. However, CD95L‐expressing tumors are rapidly rejected in
Frederik H, Igney   +2 more
openaire   +2 more sources

BAPTA-AM abrogates the cl-CD95L-mediated Ca2+ response.

open access: yes, 2023
(A) H9 T-cells were loaded with 1 mM of the calcium probe Fura-2AM for 30 min at RT. Cells were pre-incubated or not (DMSO) with BAPTA-AM (5 mM) and then stimulated with 100 ng/ml of cl-CD95L. Values were recorded every 10 s.
Eric Selva (216754)   +13 more
core   +1 more source

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