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Epigenetic Reader Bromodomain-Containing Protein 4 in Aging-Related Vascular Pathologies and Diseases: Molecular
Xiaoxu Zheng1, Kotryna Diktonaite1, Hongyu Qiu1,2
1Center for Molecular and Translational Medicine, Institute of Biomedical Science, Georgia State University, Atlanta, GA 30303, USA.
Insights
Aging accelerates vascular diseases, with Bromodomain-containing protein 4 (BRD4) emerging as a key epigenetic regulator. Understanding BRD4
Area of Science:
- Epigenetics and Molecular Biology
- Vascular Biology and Pathology
Background:
- Aging is a primary risk factor for vascular diseases, yet its regulatory mechanisms are poorly understood.
- Bromodomain-containing protein 4 (BRD4), an epigenetic regulator, is implicated in various cellular processes and increasingly linked to aging-related vascular pathology.
Purpose of the Study:
- To review recent advances in BRD4 biological function.
- To summarize studies on BRD4 in aging-associated vascular pathologies and diseases.
Main Methods:
- Literature review of recent scientific publications.
- Analysis of BRD4's role in cellular processes and disease pathogenesis.
Main Results:
- BRD4 plays diverse roles in transcription, chromatin remodeling, and DNA damage response.
- Aberrant BRD4 expression and function are associated with aging-related vascular diseases like atherosclerosis and hypertension.
Conclusions:
- BRD4 is a critical epigenetic factor in vascular aging and disease.
- Further research into BRD4 mechanisms may offer new therapeutic strategies for vascular pathologies.
Abstract:
Aging is a key independent risk factor of various vascular diseases, for which the regulatory mechanisms remain largely unknown. Bromodomain-containing protein 4 (BRD4) is a member of the Bromodomain and Extra-Terminal domain (BET) family and is an epigenetic reader playing diverse roles in regulating transcriptional elongation, chromatin remodeling, DNA damage response, and alternative splicing in various cells and tissues. While BRD4 was initially recognized for its involvement in cancer progression, recent studies have revealed that the aberrant expression and impaired function of BRD4 were highly associated with aging-related vascular pathology, affecting multiple key biological processes in the vascular cells and tissues, providing new insights into the understanding of vascular pathophysiology and pathogenesis of vascular diseases. This review summarizes the recent advances in BRD4 biological function, and the progression of the studies related to BRD4 in aging-associated vascular pathologies and diseases, including atherosclerosis, aortic aneurism vascular neointima formation, pulmonary hypertension, and essential hypertension, providing updated information to advance our understanding of the epigenetic mechanisms in vascular diseases during aging and paving the way for future research and therapeutic approaches.
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