Cellular and molecular biology of posttranslational modifications in cardiovascular disease

被引:2
作者
Zhu, Li [1 ,2 ]
Liu, Yong-Ping [3 ]
Huang, Yu-Ting [2 ]
Zhou, Zi-Jun [2 ]
Liu, Jian-Feng [4 ]
Yu, Li-Ming [2 ]
Wang, Hui-Shan [1 ,2 ]
机构
[1] Dalian Med Univ, Grad Sch, Dalian 116000, Liaoning, Peoples R China
[2] Gen Hosp Northern Theater Command, Dept Cardiovasc Surg, State Key Lab Frigid Zone Cardiovasc Dis, 83 Wenhua Rd, Shenyang 110016, Peoples R China
[3] China Med Univ, Shengjing Hosp, Dept Pediat, Shenyang 110004, Liaoning, Peoples R China
[4] Shenyang Med Coll, Sch Clin Med 1, Shenyang 110034, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
CVD; Post-translational modifications; Acetylation; Ubiquitination; HEART-FAILURE; CARDIOMYOCYTE HYPERTROPHY; LYSINE SUCCINYLATION; ATRIAL-FIBRILLATION; ENERGY-METABOLISM; CARDIAC MYOCYTES; P53; ACETYLATION; PROTEIN-KINASE; SERUM-LEVELS; SUMOYLATION;
D O I
10.1016/j.biopha.2024.117374
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cardiovascular disease (CVD) has now become the leading cause of death worldwide, and its high morbidity and mortality rates pose a great threat to society. Although numerous studies have reported the pathophysiology of CVD, the exact pathogenesis of all types of CVD is not fully understood. Therefore, much more research is still needed to explore the pathogenesis of CVD. With the development of proteomics, many studies have successfully identified the role of posttranslational modifications in the pathogenesis of CVD, including key processes such as apoptosis, cell metabolism, and oxidative stress. In this review, we summarize the progress in the understanding of posttranslational modifications in cardiovascular diseases, including novel protein posttranslational modifications such as succinylation and nitrosylation. Furthermore, we summarize the currently identified histone deacetylase (HDAC) inhibitors used to treat CVD, providing new perspectives on CVD treatment modalities. We critically analyze the roles of posttranslational modifications in the pathogenesis of CVD-related diseases and explore future research directions related to posttranslational modifications in cardiovascular diseases.
引用
收藏
页数:17
相关论文
共 158 条
[81]   Serum levels of S-glutathionylated proteins as a risk-marker for arteriosclerosis obliterans [J].
Nonaka, Kazuki ;
Kume, Noriaki ;
Urata, Yoshishige ;
Seto, Shinji ;
Kohno, Takaaki ;
Honda, Sumihisa ;
Ikeda, Soji ;
Muroya, Takahiro ;
Ikeda, Yosihiko ;
Ihara, Yoshito ;
Kita, Toru ;
Kondo, Takahito .
CIRCULATION JOURNAL, 2007, 71 (01) :100-105
[82]   SIRT5 deficiency enhances the proliferative and therapeutic capacities of adipose-derived mesenchymal stem cells via metabolic switching [J].
Ou, Tiantong ;
Yang, Wenlong ;
Li, Wenjia ;
Lu, Yijing ;
Dong, Zheng ;
Zhu, Hongming ;
Sun, Xiaolei ;
Dong, Zhen ;
Weng, Xinyu ;
Chang, Suchi ;
Li, Hua ;
Li, Yufan ;
Qiu, Zhiwei ;
Hu, Kai ;
Sun, Aijun ;
Ge, Junbo .
CLINICAL AND TRANSLATIONAL MEDICINE, 2020, 10 (05)
[83]   SIRT3 deacetylates and increases pyruvate dehydrogenase activity in cancer cells [J].
Ozden, Ozkan ;
Park, Seong-Hoon ;
Wagner, Brett A. ;
Song, Ha Yong ;
Zhu, Yueming ;
Vassilopoulos, Athanassios ;
Jung, Barbara ;
Buettner, Garry R. ;
Gius, David .
FREE RADICAL BIOLOGY AND MEDICINE, 2014, 76 :163-172
[84]   Sirt3, Mitochondrial ROS, Ageing, and Carcinogenesis [J].
Park, Seong-Hoon ;
Ozden, Ozkan ;
Jiang, Haiyan ;
Cha, Yong I. ;
Pennington, J. Daniel ;
Aykin-Burns, Nukhet ;
Spitz, Douglas R. ;
Gius, David ;
Kim, Hyun-Seok .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2011, 12 (09) :6226-6239
[85]   Phosphodiesterase 8 governs cAMP/PKA-dependent reduction of L-type calcium current in human atrial fibrillation: a novel arrhythmogenic mechanism [J].
Pavlidou, Nefeli Grammatika ;
Dobrev, Shokoufeh ;
Beneke, Kira ;
Reinhardt, Franziska ;
Pecha, Simon ;
Jacquet, Eric ;
Abu-Taha, Issam H. ;
Schmidt, Constanze ;
Voigt, Niels ;
Kamler, Markus ;
Schnabel, Renate B. ;
Baczko, Istvan ;
Garnier, Anne ;
Reichenspurner, Hermann ;
Nikolaev, Viacheslav O. ;
Dobrev, Dobromir ;
Molina, Cristina E. .
EUROPEAN HEART JOURNAL, 2023, 44 (27) :2483-2494
[86]   Restoring the epigenome in Alzheimer's disease: advancing HDAC inhibitors as therapeutic agents [J].
Pereira, Marcia ;
Cruz, Maria Teresa ;
Fortuna, Ana ;
Bicker, Joana .
DRUG DISCOVERY TODAY, 2024, 29 (07)
[87]  
Perike S, 2023, bioRxiv, DOI [10.1101/2023.04.19.537590, 10.1101/2023.04.19.537590, DOI 10.1101/2023.04.19.537590]
[88]   Honokiol blocks and reverses cardiac hypertrophy in mice by activating mitochondrial Sirt3 [J].
Pillai, Vinodkumar B. ;
Samant, Sadhana ;
Sundaresan, Nagalingam R. ;
Raghuraman, Hariharasundaram ;
Kim, Gene ;
Bonner, Michael Y. ;
Arbiser, Jack L. ;
Walker, Douglas I. ;
Jones, Dean P. ;
Gius, David ;
Gupta, Mahesh P. .
NATURE COMMUNICATIONS, 2015, 6
[89]   Strain-stimulated hypertrophy in cardiac myocytes is mediated by reactive oxygen species-dependent Ras S-glutathiolation [J].
Pimentel, David R. ;
Adachi, Takeshi ;
Ido, Yasuo ;
Heibeck, Tyler ;
Jiang, Bingbing ;
Lee, Yong ;
Melendez, J. Andres ;
Cohen, Richard A. ;
Colucci, Wilson S. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2006, 41 (04) :613-622
[90]   Phosphorylation of cardiac sodium channel at Ser571 anticipates manifestations of the aging myopathy [J].
Pizzo, Emanuele ;
Cervantes, Daniel O. ;
Ketkar, Harshada ;
Ripa, Valentina ;
Nassal, Drew M. ;
Buck, Benjamin ;
Parambath, Sreema P. ;
Di Stefano, Valeria ;
Singh, Kanwardeep ;
Thompson, Carl I. ;
Mohler, Peter J. ;
Hund, Thomas J. ;
Jacobson, Jason T. ;
Jain, Sudhir ;
Rota, Marcello .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2024, 326 (06) :H1424-H1445