Long non-coding RNAs and microRNAs as crucial regulators in cardio-oncology

被引:0
作者
Sarath Babu Nukala
Jordan Jousma
Yoonje Cho
Won Hee Lee
Sang-Ging Ong
机构
[1] The University of Illinois College of Medicine,Department of Pharmacology & Regenerative Medicine
[2] University of Arizona College of Medicine,Department of Basic Medical Sciences
[3] The University of Illinois College of Medicine,Division of Cardiology, Department of Medicine
来源
Cell & Bioscience | / 12卷
关键词
Non-coding RNAs; LncRNAs; miRNAs; Cardiotoxicity; Cardio-oncology;
D O I
暂无
中图分类号
学科分类号
摘要
Cancer is one of the leading causes of morbidity and mortality worldwide. Significant improvements in the modern era of anticancer therapeutic strategies have increased the survival rate of cancer patients. Unfortunately, cancer survivors have an increased risk of cardiovascular diseases, which is believed to result from anticancer therapies. The emergence of cardiovascular diseases among cancer survivors has served as the basis for establishing a novel field termed cardio-oncology. Cardio-oncology primarily focuses on investigating the underlying molecular mechanisms by which anticancer treatments lead to cardiovascular dysfunction and the development of novel cardioprotective strategies to counteract cardiotoxic effects of cancer therapies. Advances in genome biology have revealed that most of the genome is transcribed into non-coding RNAs (ncRNAs), which are recognized as being instrumental in cancer, cardiovascular health, and disease. Emerging studies have demonstrated that alterations of these ncRNAs have pathophysiological roles in multiple diseases in humans. As it relates to cardio-oncology, though, there is limited knowledge of the role of ncRNAs. In the present review, we summarize the up-to-date knowledge regarding the roles of long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) in cancer therapy-induced cardiotoxicities. Moreover, we also discuss prospective therapeutic strategies and the translational relevance of these ncRNAs.
引用
收藏
相关论文
共 474 条
[41]  
Fernandez-Chas M(2015)Tyrosine kinase inhibitor-associated cardiovascular toxicity in chronic myeloid leukemia J Clin Oncol 9 512-3163
[42]  
Curtis MJ(2019)Pulmonary hypertension with dasatinib and other tyrosine kinase inhibitors Pulm Circ 6 5620-494
[43]  
Niederer SA(2017)Incidence, diagnosis, and management of QT prolongation induced by cancer therapies: a systematic review J Am Heart Assoc 24 125-459
[44]  
Lakhani HV(2017)Risk of hypertension with sorafenib use in patients with cancer: a meta-analysis from 20,494 patients Am J Ther 63 927-203
[45]  
Pillai SS(2018)Management of QT prolongation induced by anti-cancer drugs: target therapy and old agents. Different algorithms for different drugs Cancer Treat Rev 54 2011-3108
[46]  
Zehra M(2009)Sorafenib-induced acute myocardial infarction due to coronary artery spasm J Cardiol 15 247-209
[47]  
Dao B(2018)Sorafenib inhibited cell growth through the MEK/ERK signaling pathway in acute promyelocytic leukemia cells Oncol Lett 33 3601-363
[48]  
Tirona MT(2019)Cardiovascular toxicity induced by kinase inhibitors: mechanisms and preclinical approaches Chem Res Toxicol 166 547-54
[49]  
Thompson E(2017)Cardiac toxicities of lapatinib in patients with breast cancer and other HER2-positive cancers: a meta-analysis Breast Cancer Res Treat 370 2451-329
[50]  
Sodhi K(2007)Cardiotoxicity associated with the tyrosine kinase inhibitor sunitinib Lancet 14 1553-271