Pathophysiological Features of Remodeling in Vascular Diseases: Impact of Inhibitor of DNA-Binding/Differentiation-3 and Estrogenic Endocrine Disruptors.

Q1 Medicine
Vincent Avecilla, Mayur Doke, Sandeep Appunni, Muni Rubens, Venkataraghavan Ramamoorthy, Jayanta Kumar Das
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Abstract

Vascular diseases, such as hypertension, atherosclerosis, cerebrovascular, and peripheral arterial diseases, present major clinical and public health challenges, largely due to their common underlying process: vascular remodeling. This process involves structural alterations in blood vessels, driven by a variety of molecular mechanisms. The inhibitor of DNA-binding/differentiation-3 (ID3), a crucial member of ID family of transcriptional regulators, has been identified as a key player in vascular biology, significantly impacting the progression of these diseases. This review explores the role of ID3 in vascular remodeling, emphasizing its involvement in processes such as apoptosis, cell proliferation, and extracellular matrix regulation. Furthermore, we examine how oxidative stress, intensified by exposure to estrogenic endocrine disruptors (EEDs) like polychlorinated biphenyls (PCBs) and bisphenol A (BPA), affects ID3 activity and contributes to vascular disease. Understanding the interaction between ID3 signaling and EED exposure provides critical insights into the molecular mechanisms underlying vascular remodeling and its role in the development and progression of vascular diseases.

血管疾病重构的病理生理特征:dna结合/分化-3抑制剂和雌激素内分泌干扰物的影响
血管疾病,如高血压、动脉粥样硬化、脑血管和外周动脉疾病,在很大程度上是由于它们共同的潜在过程:血管重塑,给临床和公共卫生带来了重大挑战。这一过程涉及血管的结构改变,由多种分子机制驱动。dna结合/分化-3 (dna binding/differentiation-3, ID3)抑制剂是转录调节因子ID家族的重要成员,在血管生物学中起着关键作用,显著影响这些疾病的进展。这篇综述探讨了ID3在血管重构中的作用,强调了它在细胞凋亡、细胞增殖和细胞外基质调节等过程中的作用。此外,我们研究了暴露于雌激素内分泌干扰物(eed)如多氯联苯(PCBs)和双酚A (BPA)时,氧化应激如何加剧,影响ID3活性并导致血管疾病。了解ID3信号和EED暴露之间的相互作用,有助于深入了解血管重塑的分子机制及其在血管疾病发生和进展中的作用。
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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来源期刊
CiteScore
9.00
自引率
0.00%
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审稿时长
6 weeks
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