Results 11 to 20 of about 2,794,922 (242)

Death receptor signaling [PDF]

open access: yesJournal of Cell Science, 2005
Apoptosis or programmed cell death is a common property of multicellular organisms ([Danial and Korsmeyer, 2004][1]; [Krammer, 2000][2]). It can be triggered by a number of factors, including UV- or γ-irradiation, chemotherapeutic drugs or signaling by death receptors (DR).
Inna, Lavrik   +2 more
openaire   +2 more sources

Genistein Sensitizes Human Cholangiocarcinoma Cell Lines to Be Susceptible to Natural Killer Cells

open access: yesBiology, 2022
Cholangiocarcinoma (CCA) is a lethal bile duct cancer, which has poor treatment outcomes due to its high resistance to chemotherapy and cancer recurrence.
Chutipa Chiawpanit   +4 more
doaj   +1 more source

microRNAs and death receptors [PDF]

open access: yesCytokine & Growth Factor Reviews, 2008
Death receptors induce apoptosis through either the Type I or II pathway. In Type I cells, the initiator caspase-8 directly activates effector caspases such as caspase-3, whereas in Type II cells, the death signal is amplified through mitochondria thereby activating effector caspases causing cell death. Recently, there have been advances in elucidating
Sun-Mi, Park, Marcus E, Peter
openaire   +2 more sources

All About (NK Cell-Mediated) Death in Two Acts and an Unexpected Encore: Initiation, Execution and Activation of Adaptive Immunity

open access: yesFrontiers in Immunology, 2022
NK cells are key mediators of immune cell-mediated cytotoxicity toward infected and transformed cells, being one of the main executors of cell death in the immune system.
Ariel Ramírez-Labrada   +24 more
doaj   +1 more source

Death receptor signals to the mitochondria [PDF]

open access: yesCancer Biology & Therapy, 2004
Apoptosis is the best-characterized form of programmed cell death (PCD) and is of fundamental importance in tissue homeostasis. In mammalian systems, there are two major pathways that are involved in the initiation of apoptosis: the "extrinsic" death receptor pathway and the "intrinsic" mitochondrial pathway.
Khosravi-Far, Roya, Esposti, Mauro Degli
openaire   +2 more sources

Targeting TRAIL Death Receptors in Triple-Negative Breast Cancers: Challenges and Strategies for Cancer Therapy

open access: yesCells, 2022
The tumor necrosis factor (TNF) superfamily member TNF-related apoptosis-inducing ligand (TRAIL) induces apoptosis in cancer cells via death receptor (DR) activation with little toxicity to normal cells or tissues.
Manjari Kundu   +3 more
doaj   +1 more source

Volatile oil of Teucrium alopecurus sensitizes colon cancer cells to TRAIL-induced cell death

open access: yesFrontiers in Bioscience-Scholar, 2021
TNF-related apoptosis-inducing ligand (TRAIL/Apo2L), a member of cytokine family, is known to selectively induce apoptosis in cancer cells. However, developing resistance to TRAIL is a major obstacle in cancer therapy.
Fatma Guesmi   +7 more
doaj   +1 more source

Oxaliplatin resistance in colorectal cancer enhances TRAIL sensitivity via death receptor 4 upregulation and lipid raft localization

open access: yeseLife, 2021
Colorectal cancer (CRC) remains a leading cause of cancer death, and its mortality is associated with metastasis and chemoresistance. We demonstrate that oxaliplatin-resistant CRC cells are sensitized to TRAIL-mediated apoptosis.
Joshua D Greenlee   +6 more
doaj   +1 more source

TRAF2 Controls Death Receptor-Induced Caspase-8 Processing and Facilitates Proinflammatory Signaling

open access: yesFrontiers in Immunology, 2019
Tumor necrosis factor (TNF) receptor associated factor-2 (TRAF2) knockout (KO) cells were generated to investigate the role of TRAF2 in signaling by TNFR1 and the CD95-type death receptors (DRs) TRAILR1/2 and CD95.
Jennifer Kreckel   +4 more
doaj   +1 more source

Differential activation of JNK1 isoforms by TRAIL receptors modulate apoptosis of colon cancer cell lines [PDF]

open access: yes, 2009
Tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) induces apoptosis on binding to its receptors, death receptor 4 and 5 (DR4, DR5).
M Keane   +11 more
core   +1 more source

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