Gene Therapy for Cardiomyocyte Renewal: Cell Cycle, a Potential Therapeutic Target

被引:3
|
作者
Son, Yura [1 ,2 ]
Zhu, Wuqiang [1 ,2 ]
机构
[1] Mayo Clin Arizona, Dept Cardiovasc Dis, Dept Physiol & Biomed Engn, Scottsdale, AZ 85259 USA
[2] Mayo Clin Arizona, Ctr Regenerat Med, Scottsdale, AZ 85259 USA
关键词
NANOPARTICLE-MEDIATED DELIVERY; CHRONIC MYOCARDIAL-ISCHEMIA; HEART REGENERATION; CARDIAC-FUNCTION; DNA-SYNTHESIS; DIFFERENTIATED CARDIOMYOCYTES; ADENOASSOCIATED VIRUSES; ADULT CARDIOMYOCYTES; LENTIVIRAL VECTOR; DOUBLE-BLIND;
D O I
10.1007/s40291-022-00625-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Heart disease is the primary cause of death worldwide. Even though extensive research has been done, and many pharmacological and surgical treatments have been introduced to treat heart disease, the mortality rate still remains high. Gene therapy is widely used to understand molecular mechanisms of myocardial infarction and to treat cardiomyocyte loss. It was reported that adult cardiomyocytes proliferate at a very low rate; thus, targeting their proliferation has become a new regenerative therapeutic approach. Currently, re-activating cardiomyocyte proliferation appears to be one of the most promising methods to promote adult cardiomyocyte renewal. In this article, we highlight gene therapeutic targets of cell proliferation presently being pursued to re-activate the cell cycle of cardiomyocytes, including cell cycle regulators, transcription factors, microRNAs, signal transduction, and other contributing factors. We also summarize gene delivery vectors that have been used in cardiac research and major challenges to be overcome in the translation to the clinical approach and future directions.
引用
收藏
页码:129 / 140
页数:12
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