Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/287554
COMPARTIR / EXPORTAR:
SHARE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Título: | Restoring TRAILR2/DR5-Mediated Activation of Apoptosis upon Endoplasmic Reticulum Stress as a Therapeutic Strategy in Cancer |
Autor: | Mora-Molina, Rocío CSIC ORCID; López-Rivas, Abelardo CSIC ORCID | Palabras clave: | Apoptosis Extrinsic pathway TRAILR2/DR5 FLIP Cancer Endoplasmic reticulum stress Unfolded protein response Tumor microenvironment |
Fecha de publicación: | 2022 | Editor: | Molecular Diversity Preservation International | Citación: | International Journal of Molecular Sciences 23(16): 8987 (2022) | Resumen: | The uncontrolled proliferation of malignant cells in growing tumors results in the generation of different stressors in the tumor microenvironment, such as nutrient shortage, hypoxia and acidosis, among others, that disrupt endoplasmic reticulum (ER) homeostasis and may lead to ER stress. As a response to ER stress, both normal and tumor cells launch a set of signaling pathways known as the unfolded protein response (UPR) to restore ER proteostasis and maintain cell viability and function. However, under sustained ER stress, an apoptotic cell death process can be induced and this has been the subject of different review articles, although the role of the TRAIL-R2/DR5-activated extrinsic pathway of apoptosis has not yet been thoroughly summarized. In this Review, we provide an updated overview of the molecular mechanisms regulating cell fate decisions in tumor cells undergoing ER stress and discuss the role of the tumor necrosis factor (TNF)-related apoptosis-inducing ligand receptor 2 (TRAIL-R2/DR5) in the final outcome of UPR signaling. Particularly, we focus on the mechanisms controlling cellular FLICE-like inhibitory protein (FLIP) levels in tumor cells undergoing ER stress, which may represent a potential target for therapeutic intervention in cancer. | Versión del editor: | http://dx.doi.org/10.3390/ijms23168987 | URI: | http://hdl.handle.net/10261/287554 | DOI: | 10.3390/ijms23168987 | Identificadores: | doi: 10.3390/ijms23168987 e-issn: 1422-0067 issn: 1661-6596 |
Aparece en las colecciones: | (CABIMER) Artículos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
ijms-23-08987.pdf | 2,45 MB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
Page view(s)
32
checked on 27-abr-2024
Download(s)
41
checked on 27-abr-2024
Google ScholarTM
Check
Altmetric
Altmetric
Este item está licenciado bajo una Licencia Creative Commons