细胞质多腺苷酸化酶结合蛋白 1 与动脉粥样硬化:前瞻性目标和新见解

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-01-01 DOI:10.2174/0115701611258090231221082502
Jing Zhou, Chao-Ke Tang
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引用次数: 0

摘要

核糖核酸(RNA)结合蛋白细胞质多腺苷酸化元件结合蛋白 1(CPEB1)是 CPEB 家族的重要成员,在控制基因表达方面对健康生理和病理过程都至关重要。CPEB1 可与底物信使核糖核酸(mRNA)的 3'- 非翻译区(UTR)结合,并调节其翻译。越来越多的证据表明,CPEB1 与动脉粥样硬化的病理基础密切相关。根据最近的研究,许多病理过程,包括炎症、脂质代谢、内皮功能障碍、血管生成、氧化应激、细胞衰老、细胞凋亡和胰岛素抵抗,都受 CPEB1 的调控。本综述结合 CPEB1 生理功能的演变、最新研究突破以及 CPEB1 在动脉粥样硬化中的潜在参与,探讨了动脉粥样硬化性心脏病的预防和治疗。
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Cytoplasmic Polyadenylation Element Binding Protein 1 and Atherosclerosis: Prospective Target and New Insights.

The ribonucleic acid (RNA)-binding protein Cytoplasmic Polyadenylation Element Binding Protein 1 (CPEB1), a key member of the CPEB family, is essential in controlling gene expression involved in both healthy physiological and pathological processes. CPEB1 can bind to the 3'- untranslated regions (UTR) of substrate messenger ribonucleic acid (mRNA) and regulate its translation. There is increasing evidence that CPEB1 is closely related to the pathological basis of atherosclerosis. According to recent investigations, many pathological processes, including inflammation, lipid metabolism, endothelial dysfunction, angiogenesis, oxidative stress, cellular senescence, apoptosis, and insulin resistance, are regulated by CPEB1. This review considers the prevention and treatment of atherosclerotic heart disease in relation to the evolution of the physiological function of CPEB1, recent research breakthroughs, and the potential participation of CPEB1 in atherosclerosis.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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