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Elucidation of Epigenetic Landscape in Coronary Artery Disease: A Review on Basic Concept to Personalized Medicine

机译:鉴定冠状动脉疾病中的表观遗工阐释:对个性化医学的基本概念综述

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摘要

Despite extensive clinical research and management protocols applied in the field of coronary artery diseases (CAD), it still holds the number 1 position in mortality worldwide. This indicates that we need to work on precision medicine to discover the diagnostic, therapeutic, and prognostic targets to improve the outcome of CAD. In precision medicine, epigenetic changes play a vital role in disease onset and progression. Epigenetics is the study of heritable changes that do not affect the alterations of DNA sequence in the genome. It comprises various covalent modifications that occur in DNA or histone proteins affecting the spatial arrangement of the DNA and histones. These multiple modifications include DNA/histone methylation, acetylation, phosphorylation, and SUMOylation. Besides these covalent modifications, non-coding RNAs—viz. miRNA, lncRNA, and circRNA are also involved in epigenetics. Smoking, alcohol, diet, environmental pollutants, obesity, and lifestyle are some of the prime factors affecting epigenetic alterations. Novel molecular techniques such as next-generation sequencing, chromatin immunoprecipitation, and mass spectrometry have been developed to identify important cross points in the epigenetic web in relation to various diseases. The studies regarding exploration of epigenetics, have led researchers to identify multiple diagnostic markers and therapeutic targets that are being used in different disease diagnosis and management. Here in this review, we will discuss various ground-breaking contributions of past and recent studies in the epigenetic field in concert with coronary artery diseases. Future prospects of epigenetics and its implication in CAD personalized medicine will also be discussed in brief.
机译:尽管在冠状动脉疾病(CAD)领域应用了广泛的临床研究和管理方案,但它仍然持有全球死亡率的1号位置。这表明我们需要研究精确药物以发现改善CAD结果的诊断,治疗和预后靶标。在精确的药物中,表观遗传变化在疾病发作和进展中起着至关重要的作用。表观遗传学是研究遗传变化,不会影响基因组中DNA序列的变化。它包括在影响DNA和组蛋白的空间排列的DNA或组蛋白中发生的各种共价修饰。这些多种修饰包括DNA /组甲基化,乙酰化,磷酸化和SuMoylation。除了这些共价修改之外,非编码RNA-viz。 miRNA,Lncra和Circrna也参与表观遗传学。吸烟,酒精,饮食,环境污染物,肥胖和生活方式是影响表观遗传改变的主要因素。已经开发出新的分子技术,例如下一代测序,染色质免疫沉淀和质谱法,以鉴定与各种疾病相关的表观遗传网中的重要交叉点。关于表观遗传学探索的研究引领了研究人员,以鉴定在不同疾病诊断和管理中使用的多种诊断标记和治疗靶标。在此评论中,我们将在冠心病疾病中讨论过去和最近研究表观遗传领域的各种接地贡献。简要介绍,外观遗传学的未来前景及其在CAD个性化医学中的含义。

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