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血管钙化的组学研究。

Omics research in vascular calcification.

机构信息

Research Lab of Translational Medicine, Hengyang Medical School, University of South China, Hengyang 421001, China; Guangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin 541100, China.

Guangxi Key Laboratory of Diabetic Systems Medicine, Guilin Medical University, Guilin 541100, China.

出版信息

Clin Chim Acta. 2020 Dec;511:319-328. doi: 10.1016/j.cca.2020.10.022. Epub 2020 Oct 21.

DOI:10.1016/j.cca.2020.10.022
PMID:33096035
Abstract

Vascular calcification (VC), the pathological process of hydroxyapatite mineral deposition in the vascular system, is closely associated with aging, atherosclerotic plaque formation, cardiovascular disease (CVD) and diabetes mellitus (DM). Studies have shown that VC is related to cellular phenotypic changes, extracellular vesicles, disordered calcium and phosphate homeostasis, and an imbalance between inducers and inhibitors of VC. Unfortunately, there is currently no effective preventive or targeted treatment for pathologic condition. The rapid evolution of omics technology (genomics, epigenomics, transcriptomics, proteomics and metabolomics) has provided a novel approach for elucidation of pathophysiologic mechanisms in general and those associated with VC specifically. Here, we review articles published over the last twenty years and focus on the current state, challenges, limitations and future of omics in VC research and clinical practice. Highlighting potential targets based on omics technology will improve our understanding of this pathologic condition and assist in the development of potential treatment options for VC related disease.

摘要

血管钙化(VC)是指羟基磷灰石在血管系统中的病理性沉积过程,与衰老、动脉粥样硬化斑块形成、心血管疾病(CVD)和糖尿病(DM)密切相关。研究表明,VC 与细胞表型变化、细胞外囊泡、钙和磷稳态紊乱以及 VC 诱导剂和抑制剂之间的失衡有关。不幸的是,目前对于这种病理状况还没有有效的预防或靶向治疗方法。组学技术(基因组学、表观基因组学、转录组学、蛋白质组学和代谢组学)的快速发展为阐明一般生理病理机制以及与 VC 相关的机制提供了一种新方法。在这里,我们回顾了过去二十年发表的文章,重点介绍了组学在 VC 研究和临床实践中的现状、挑战、局限性和未来。基于组学技术突出潜在靶点将有助于我们更好地理解这种病理状况,并有助于开发针对 VC 相关疾病的潜在治疗方法。

相似文献

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Omics research in vascular calcification.血管钙化的组学研究。
Clin Chim Acta. 2020 Dec;511:319-328. doi: 10.1016/j.cca.2020.10.022. Epub 2020 Oct 21.
2
Omics research in vascular calcification.血管钙化的组学研究。
Clin Chim Acta. 2020 Dec;511:198-207. doi: 10.1016/j.cca.2020.10.021. Epub 2020 Oct 21.
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A multi-omics view of the complex mechanism of vascular calcification.多组学视角下的血管钙化复杂机制。
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Diabetes and calcification: The potential role of anti-diabetic drugs on vascular calcification regression.糖尿病与钙化:抗糖尿病药物在血管钙化消退中的潜在作用。
Pharmacol Res. 2020 Aug;158:104861. doi: 10.1016/j.phrs.2020.104861. Epub 2020 May 11.
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Exosomes, the message transporters in vascular calcification.外泌体:血管钙化中的信息转运体。
J Cell Mol Med. 2018 Sep;22(9):4024-4033. doi: 10.1111/jcmm.13692. Epub 2018 Jun 12.
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The molecular biology and pathophysiology of vascular calcification.血管钙化的分子生物学和病理生理学。
Postgrad Med. 2014 Mar;126(2):54-64. doi: 10.3810/pgm.2014.03.2740.
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Label-free quantitative proteomics identifies Smarca4 is involved in vascular calcification.无标记定量蛋白质组学鉴定 Smarca4 参与血管钙化。
Ren Fail. 2019 Nov;41(1):220-228. doi: 10.1080/0886022X.2019.1591997.
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A narrative review of exosomes in vascular calcification.血管钙化中外泌体的叙述性综述。
Ann Transl Med. 2021 Apr;9(7):579. doi: 10.21037/atm-20-7355.
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Roles of Histone Acetylation Modifiers and Other Epigenetic Regulators in Vascular Calcification.组蛋白乙酰化修饰酶和其他表观遗传调控因子在血管钙化中的作用。
Int J Mol Sci. 2020 May 4;21(9):3246. doi: 10.3390/ijms21093246.
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OGT knockdown counteracts high phosphate-induced vascular calcification in chronic kidney disease through autophagy activation by downregulating YAP.OGT 敲低通过下调 YAP 激活自噬来拮抗高磷诱导的慢性肾脏病血管钙化。
Life Sci. 2020 Nov 15;261:118121. doi: 10.1016/j.lfs.2020.118121. Epub 2020 Jul 18.

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