端粒酶
端粒
疾病
端粒酶逆转录酶
逆转录酶
表型
癌症研究
冠状动脉疾病
端粒酶RNA组分
生物信息学
医学
核糖核酸
遗传学
生物
病理
内科学
DNA
基因
作者
Jedrzej Hoffmann,Gavin D. Richardson,Judith Haendeler,Joachim Altschmied,Vicente Andrés,Ioakim Spyridopoulos
标识
DOI:10.1161/atvbaha.120.315695
摘要
Shortened telomeres have been linked to numerous chronic diseases, most importantly coronary artery disease, but the underlying mechanisms remain ill defined. Loss-of-function mutations and deletions in telomerase both accelerate telomere shortening but do not necessarily lead to a clinical phenotype associated with atherosclerosis, questioning the causal role of telomere length in cardiac pathology. The differential extranuclear functions of the 2 main components of telomerase, telomerase reverse transcriptase and telomerase RNA component, offer important clues about the complex relationship between telomere length and cardiovascular pathology. In this review, we critically discuss relevant preclinical models, genetic disorders, and clinical studies to elucidate the impact of telomerase in cardiovascular disease and its potential role as a therapeutic target. We suggest that the antioxidative function of mitochondrial telomerase reverse transcriptase might be atheroprotective, making it a potential target for clinical trials. Graphic Abstract: A graphic abstract is available for this article.
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