{"title":"Telomere and Telomerase Biology in Cardiovascular Disease: A State-of-the-art Review and Outlook","authors":"Xian Wen Tan, Alan Yean Yip Fong","doi":"10.15420/japsc.2023.26","DOIUrl":null,"url":null,"abstract":"Telomeres are short repetitive hexanucleotides located at the ends of eukaryotic DNA sequences. They progressively shorten with each mitotic cycle, and telomerase counteracts the process by regulating and extending the telomeres. Ageing, oxidative stress and inflammation are predisposing factors that accelerate telomere shortening, and eventually drive cells to senescence. Recent findings have observed the associations of short telomere length with traditional cardiovascular risk factors leading to cardiovascular phenotype. However, such association remains hypothesised as a reserved causation, mainly confounded by unfathomable covariates and mixed research findings. Based on the recent literature, the present review aimed to provide a concise update and diverging view on telomere−telomerase biology in cardiovascular disease.","PeriodicalId":321604,"journal":{"name":"Journal of Asian Pacific Society of Cardiology","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Asian Pacific Society of Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15420/japsc.2023.26","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Telomeres are short repetitive hexanucleotides located at the ends of eukaryotic DNA sequences. They progressively shorten with each mitotic cycle, and telomerase counteracts the process by regulating and extending the telomeres. Ageing, oxidative stress and inflammation are predisposing factors that accelerate telomere shortening, and eventually drive cells to senescence. Recent findings have observed the associations of short telomere length with traditional cardiovascular risk factors leading to cardiovascular phenotype. However, such association remains hypothesised as a reserved causation, mainly confounded by unfathomable covariates and mixed research findings. Based on the recent literature, the present review aimed to provide a concise update and diverging view on telomere−telomerase biology in cardiovascular disease.
端粒是位于真核生物 DNA 序列末端的短小重复六核苷酸。端粒在每个有丝分裂周期中逐渐缩短,端粒酶通过调节和延长端粒来抵消这一过程。衰老、氧化应激和炎症是加速端粒缩短的诱发因素,并最终导致细胞衰老。最近的研究发现,端粒长度短与导致心血管表型的传统心血管风险因素有关。然而,这种关联仍被假定为一种保留的因果关系,主要受到深不可测的协变量和混杂的研究结果的影响。根据最近的文献,本综述旨在提供有关心血管疾病中端粒-端粒酶生物学的最新简明信息和不同观点。