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Review
. 2022 Jul 29:2022:7439878.
doi: 10.1155/2022/7439878. eCollection 2022.

Oxidative Stress-Induced Protein of SESTRIN2 in Cardioprotection Effect

Affiliations
Review

Oxidative Stress-Induced Protein of SESTRIN2 in Cardioprotection Effect

Huang Rongjin et al. Dis Markers. .

Abstract

Because of the rich mitochondria and high energy metabolic requirements, excessive oxidative stress generated by ROS is a key pathogenic mechanism in heart disease. SESTRIN2, the well-known antioxidant protein, plays a vital role in diminishing the production and accumulation of ROS, thus sparing cells from oxidative damage. From this new perspective, we first examine SESTRIN2 structure-function relationships; then, we describe how SESTRIN2 expression is regulated under oxidative stress conditions, emphasizing SESTRIN2's antioxidant mechanism via multiple signal transductions; and finally, we discuss SESTRIN2's role in a variety of oxidative stress-related cardiac diseases, including age-related heart disease, diabetic cardiomyopathy, ischemia-reperfusion myocardial injury, septic cardiomyopathy, and chronic cardiac insufficiency. The goal of this review is to identify the SESTRIN2 protein as a potential biomarker and new therapy target for oxidative stress-related cardiac diseases.

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Conflict of interest statement

The authors declare that there are no potential conflicts of interest.

Figures

Figure 1
Figure 1
Schematic representation of the full-length gene sequence of SESN2 showing the three structural domains SESN-A, SESN-B, and SESN-C; schematic representation of the spatial structure of SESTRIN2 showing the SESN-A redox site (C125), the SESN-C physical interaction site with GATOR2 and the leucine binding site.
Figure 2
Figure 2
Schematic diagram of the biological effects of SESTRIN2 against oxidative stress.

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