Apoptotic cell death in disease-Current understanding of the NCCD 2023
Research output: Contribution to journal › Review article › Contributed › peer-review
Contributors
- Italian Institute for Genomic Medicine (IIGM)
- Karolinska Institutet
- Weill Cornell Medical College in Qatar
- Icahn School of Medicine at Mount Sinai
- University of Texas Southwestern Medical Center
- Kiel University
- University of Rome Tor Vergata
- Thomas Jefferson University
- University of Campania Luigi Vanvitelli
- University of Konstanz
- Sunnybrook Health Science Centre
- Hebrew University of Jerusalem
- Weizmann Institute of Science
- University of Massachusetts Medical School
- Fox Chase Cancer Center
- German Center for Neurodegenerative Diseases (DZNE)
- Nazarbayev University
- Louisiana State University Health Sciences Center
- Friedrich-Alexander University Erlangen-Nürnberg
- VIB-UGent Center for Inflammation Research
- University of Connecticut
- Roswell Park Comprehensive Cancer Center
- Cornell University
- IRCCS Istituti fisioterapici ospitalieri - Istituto Regina Elena
- University of Freiburg
- Centro de Investigaciones Biologicas Margarita Salas
- Université Paris-Saclay
- University of Lausanne
- Technical University of Denmark
- University of Texas at Austin
- Queen Mary University of London
- University of Hawai'i at Mānoa
- Graz University of Technology
- Center for Autophagy
- Duke University
- Shanghai Jiao Tong University
- Nankai University
- Shenzhen Institute of Advanced Technology (SIAT)
- Memorial Sloan-Kettering Cancer Center
- KU Leuven
Abstract
Apoptosis is a form of regulated cell death (RCD) that involves proteases of the caspase family. Pharmacological and genetic strategies that experimentally inhibit or delay apoptosis in mammalian systems have elucidated the key contribution of this process not only to (post-)embryonic development and adult tissue homeostasis, but also to the etiology of multiple human disorders. Consistent with this notion, while defects in the molecular machinery for apoptotic cell death impair organismal development and promote oncogenesis, the unwarranted activation of apoptosis promotes cell loss and tissue damage in the context of various neurological, cardiovascular, renal, hepatic, infectious, neoplastic and inflammatory conditions. Here, the Nomenclature Committee on Cell Death (NCCD) gathered to critically summarize an abundant pre-clinical literature mechanistically linking the core apoptotic apparatus to organismal homeostasis in the context of disease.
Details
Original language | English |
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Pages (from-to) | 1097-1154 |
Number of pages | 58 |
Journal | Cell death and differentiation |
Volume | 30 |
Issue number | 5 |
Publication status | Published - May 2023 |
Peer-reviewed | Yes |
External IDs
PubMedCentral | PMC10130819 |
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Scopus | 85153609153 |
ORCID | /0000-0001-6874-0548/work/148143851 |
ORCID | /0000-0001-6287-9725/work/148145950 |
Keywords
Sustainable Development Goals
Keywords
- Animals, Humans, Apoptosis/genetics, Cell Death, Caspases/genetics, Carcinogenesis, Mammals/metabolism