TNF-Related Apoptosis-Inducing Ligand: Non-Apoptotic Signalling.

EMT TNF TRAIL apoptosis cancer metastasis migration signalling

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
16 Mar 2024
Historique:
received: 07 02 2024
revised: 01 03 2024
accepted: 14 03 2024
medline: 27 3 2024
pubmed: 27 3 2024
entrez: 27 3 2024
Statut: epublish

Résumé

TNF-related apoptosis-inducing ligand (TRAIL or Apo2 or TNFSF10) belongs to the TNF superfamily. When bound to its agonistic receptors, TRAIL can induce apoptosis in tumour cells, while sparing healthy cells. Over the last three decades, this tumour selectivity has prompted many studies aiming at evaluating the anti-tumoral potential of TRAIL or its derivatives. Although most of these attempts have failed, so far, novel formulations are still being evaluated. However, emerging evidence indicates that TRAIL can also trigger a non-canonical signal transduction pathway that is likely to be detrimental for its use in oncology. Likewise, an increasing number of studies suggest that in some circumstances TRAIL can induce, via Death receptor 5 (DR5), tumour cell motility, potentially leading to and contributing to tumour metastasis. While the pro-apoptotic signal transduction machinery of TRAIL is well known from a mechanistic point of view, that of the non-canonical pathway is less understood. In this study, we the current state of knowledge of TRAIL non-canonical signalling.

Identifiants

pubmed: 38534365
pii: cells13060521
doi: 10.3390/cells13060521
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European union
ID : MSCA-2022-SE-01-01
Organisme : European union
ID : 777995
Organisme : Agence Nationale de la Recherche
ID : ANR22-LCV1-0005-01
Organisme : Agence Nationale de la Recherche
ID : ANR-11LABX-0021-01
Organisme : Agence Nationale de la Recherche
ID : ANR-15-IDEX-0003
Organisme : French National Cancer Institute
ID : PLBIO22-171

Auteurs

Abderrahmane Guerrache (A)

Université de Bourgogne, 21000 Dijon, France.
INSERM Research Center U1231, «Equipe DesCarTes», 21000 Dijon, France.

Olivier Micheau (O)

Université de Bourgogne, 21000 Dijon, France.
INSERM Research Center U1231, «Equipe DesCarTes», 21000 Dijon, France.
Laboratoire d'Excellence LipSTIC, 21000 Dijon, France.

Classifications MeSH