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ATF3 in atherosclerosis: a controversial transcription factor
Bingyu Wang1, Xi Yang1,2,3, Xinyi Sun1
1Department of Cardiovascular, Medical College, Ningbo University, Ningbo, China.
Activated transcription factor 3 (ATF3) has dual roles in atherosclerosis. While it worsens inflammation in endothelial cells, ATF3 regulates inflammation and cholesterol metabolism in macrophages and liver cells, offering therapeutic potential.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Gene Regulation
Background:
- Atherosclerosis is a major cause of cardiovascular disease globally.
- Transcription factors are crucial regulators of cellular processes and disease progression in atherosclerosis.
- Activated transcription factor 3 (ATF3), part of the ATF/cAMP response element binding (CREB) family, modulates gene expression.
Purpose of the Study:
- To review the mechanism, structure, and pathophysiological roles of ATF3 in atherosclerosis.
- To elucidate the distinct functions of ATF3 in different cell types involved in atherosclerosis.
- To explore the therapeutic potential of ATF3 for atherosclerosis treatment.
Main Methods:
- Literature review focusing on ATF3's role in atherosclerosis.
- Analysis of ATF3's function in vascular endothelial cells, macrophages, and liver cells.
- Examination of ATF3's structure and its impact on gene transcription.
Main Results:
- ATF3 overexpression in endothelial cells exacerbates oxidative stress and inflammation.
- In macrophages and liver cells, ATF3 acts as an anti-inflammatory agent and promotes cholesterol metabolism.
- ATF3 exhibits context-dependent roles in the pathogenesis of atherosclerosis.
Conclusions:
- ATF3 has a complex, cell-specific role in atherosclerosis.
- Targeting ATF3 presents a potential therapeutic strategy for atherosclerosis.
- Understanding ATF3's dual functions is key for developing novel cardiovascular disease treatments.
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