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Role of apoptosis repressor with caspase recruitment domain in human health and chronic diseases.
- Source :
-
Annals of medicine [Ann Med] 2024 Dec; Vol. 56 (1), pp. 2409958. Date of Electronic Publication: 2024 Oct 01. - Publication Year :
- 2024
-
Abstract
- Apoptosis repressor with caspase recruitment domain (ARC) is a highly potent and multifunctional suppressor of various types of programmed cell death (PCD) (e.g. apoptosis, necroptosis, and pyroptosis) and plays a key role in determining cell fate. Under physiological conditions, ARC is predominantly expressed in terminally differentiated cells, such as cardiomyocytes and skeletal muscle cells. Its expression and activity are tightly controlled by a complicated system consisting of transcription factor (TF), non-coding RNA (ncRNA), and post-translational modification (PTM). ARC dysregulation has been shown to be closely associated with many chronic diseases, including cardiovascular disease, cancer, diabetes, and neurodegenerative disease. However, the detailed mechanisms of ARC involved in the progression of these diseases remain unclear to a large extent. In this review, we mainly focus on the regulatory mechanisms of ARC expression and activity and its role in PCD. We also discuss the underlying mechanisms of ARC in health and disease and highlight the potential implications of ARC in the clinical treatment of patients with chronic diseases. This information may assist in developing ARC-based therapeutic strategies for patients with chronic diseases and expand researchers' understanding of ARC.
- Subjects :
- Humans
Chronic Disease
Neoplasms metabolism
Neoplasms pathology
Neoplasms genetics
Cardiovascular Diseases metabolism
Protein Processing, Post-Translational
Neurodegenerative Diseases metabolism
Neurodegenerative Diseases genetics
Caspase Activation and Recruitment Domain
Diabetes Mellitus metabolism
Muscle Proteins
Apoptosis
Apoptosis Regulatory Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2060
- Volume :
- 56
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Annals of medicine
- Publication Type :
- Academic Journal
- Accession number :
- 39351758
- Full Text :
- https://doi.org/10.1080/07853890.2024.2409958