受体酪氨酸激酶:仍然是抑制血管平滑肌细胞增殖的有趣靶点

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS American Journal of Cardiovascular Drugs Pub Date : 2023-07-31 DOI:10.1007/s40256-023-00596-3
Yilin Xiong, Yan Wang, Tao Yang, Yunmei Luo, Shangfu Xu, Lisheng Li
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引用次数: 1

摘要

血管平滑肌细胞(VSMCs)增殖是导致血管重塑(如高血压、再狭窄和肺动脉高压)的关键事件。越来越多的证据表明,VSMCs的增殖与受体酪氨酸激酶(RTKs)通过其配体的激活有关,包括胰岛素样生长因子受体(IGFR)、成纤维细胞生长因子受体、表皮生长因子受体,血管内皮生长因子受体和血小板衍生生长因子受体。此外,已经发现了一些受体酪氨酸酶抑制剂(TKIs),它们可以阻止VSMCs增殖以减轻血管重塑。因此,本文将介绍RTKs及其抑制剂在控制VSMCs增殖中的作用的最新研究进展,这有助于更好地了解VSMCs增殖在心血管事件中的作用,有利于血管疾病的预防和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Receptor Tyrosine Kinase: Still an Interesting Target to Inhibit the Proliferation of Vascular Smooth Muscle Cells

Vascular smooth muscle cells (VSMCs) proliferation is a critical event that contributes to the pathogenesis of vascular remodeling such as hypertension, restenosis, and pulmonary hypertension. Increasing evidences have revealed that VSMCs proliferation is associated with the activation of receptor tyrosine kinases (RTKs) by their ligands, including the insulin-like growth factor receptor (IGFR), fibroblast growth factor receptor (FGFR), epidermal growth factor receptor (EGFR), vascular endothelial growth factor receptor (VEGFR), and platelet-derived growth factor receptor (PDGFR). Moreover, some receptor tyrosinase inhibitors (TKIs) have been found and can prevent VSMCs proliferation to attenuate vascular remodeling. Therefore, this review will describe recent research progress on the role of RTKs and their inhibitors in controlling VSMCs proliferation, which helps to better understand the function of VSMCs proliferation in cardiovascular events and is beneficial for the prevention and treatment of vascular disease.

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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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