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心血管疾病与表观遗传学研究进展 被引量:11

Research progress of epigenetics in cardiovascular disease
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摘要 心血管疾病是环境与遗传因素共同影响的复杂疾病,DNA密码决定其是否发病。全基因组关联研究结果发现,存在于编码序列中的遗传密码并非心血管疾病的全部影响因素,隐藏在非编码序列中的遗传机制更能说明环境因素对心血管疾病的影响。在不改变DNA编码序列和染色质结构前提下对基因表达进行调控的机制被称为表观遗传学,主要包括DNA甲基化和羟甲基化、组蛋白修饰和RNA相关机制。本文就表观遗传学在心血管疾病研究中的重要性、表观遗传学的基本机制及其在心血管疾病诊断和治疗中的应用进展作一综述。 As a complex disease influenced jointly by environmental and genetic factors, the attack of cardiovascular disease is mainly determined by DNA code. Whereas Genome-wide Association Study (GWAS) has found that the hidden genetic mechanism in the non-coding sequences may better illustrate how environment affects the attack of the disease, besides the genetic code existing in coding sequences. It is defined as epigenetics to regulate gene expression without altering DNA coding sequences and chromatin structures, which mainly includes DNA methylation and hydroxyl methylation, histone modification and RNA related mechanisms. This paper reviews the research progress of the importance of epigenetics in cardiovascular disease, the basic mechanism of epigenetles, and the application of epigenetics in the diagnosis and treatment of cardiovascular disease.
出处 《中华实用诊断与治疗杂志》 2016年第5期426-428,共3页 Journal of Chinese Practical Diagnosis and Therapy
基金 河南省科技厅重点攻关项目(122102310620)
关键词 心血管疾病 冠心病 表观遗传学 甲基化 组蛋白修饰 INK4位点中反义非编码RNA Cardiovascular disease coronary heart disease epigenetics methylation histone modification antisense non-coding RNA in the INK4 locus
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参考文献23

  • 1陈伟伟,高润霖,刘力生,朱曼璐,王文,王拥军,吴兆苏,李惠君,郑哲,蒋立新,胡盛寿.《中国心血管病报告2014》概要[J].中国循环杂志,2015,30(7):617-622. 被引量:796
  • 2Yang G, Wang Y, Zeng Y, et al. Rapid health transition in China, 1990 2010: findings from the Global Burden of Disease Study[J]. Lancet,2013,381(9882):1964-1966.
  • 3Murray CJ, Barber RM, Foreman KJ, et al. Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990-2013: quantifying the epidemiological transition[J]. Lancet,2015,386(10009) :2145 2191.
  • 4Massimo M, Tim S. Understanding coronary artery disease using twin studies[J]. Heart, 2013,99 (6):373 375.
  • 5Nagy C, Turecki G. Transgenerational epigenetic inheritance: an open discussion[J] Epigenomics, 2015,7 (5) : 781 790.
  • 6Ito S, Shen L, Dai Q, et al. Tet proteins can convert 5- methylcytosine to 5-formylcytosine and 5 carboxylcytosine[J]. Science,2011,333(6047) : 1300-1303.
  • 7Minjia T, Hao L, Sangkyu L, et al. Identification of 67 histone marks and histone lysine crotonylation as a new type of histone modification[J]. Ce11,2011,146(6) : 1016-1028.
  • 8Rinn JL, Chang HY. Genome regulation by long noncoding RNAs[J]. Annu Rev Biochem, 2012,81 (7) 145 166.
  • 9Lee JT, Bartolomei MS. X-inactivation, imprinting, and long non-coding RNAs in health and disease[J]. Cell, 2013,152 ( 6 ) : 1308 1323.
  • 10Haraguchi Y, Shimizu T, Yamato M, et al. Concise review: cell therapy and tissue engineering for cardiovascular disease [J]. Stem CellTransl Med,2012,1(2):136 141.

二级参考文献30

  • 1丁小燕,欧杰雄,马红婕,闫宏,唐仕波.糖尿病性视神经病变的临床分析[J].中国实用眼科杂志,2005,23(12):1269-1274. 被引量:52
  • 2王佐,童中艺,周晓峰,姜志胜,唐朝克,宋砚明,田永凤.微孔法分离大鼠骨髓内皮祖细胞[J].生物化学与生物物理进展,2007,34(7):754-759. 被引量:10
  • 3Miyahara K,Kawamoto T,Sase K,et al.Cloning and structural characterization of the human endothelial nitric oxide synthase gene[J].Eur J Biochem,1994,223(3):719-726.
  • 4Taniwaki H,Ishimura E,Matsumoto N,et al.Relations between ACE gene and ecNOS gene polymorphisms and resistive index in type 2 diabetic patients with nephropathy[J].Diabetes Care,2001,24(1):1653-1660.
  • 5Awata T,Neda T,Iizuka H,et al.Endothelial nitric oxide syn thase gene is associated with diabetic macular edema in type 2 diabetes[J].Diabetes Care 2004,27(9):2184-2190.
  • 6Wascher TC,Graier WF,Bahadori B,et al.Time course of endothelial dysfunction in diabetes mellitus[J].Circulation,1994,90(2):1109-1110.
  • 7Frost D,Chitu J,Meyer M,et al.Endothelial nitric oxide synthase (ecNOS) 4a /b gene polymorphism and carotid artery intima media thick ness in type1 diabetic patients[J].Exp Clin Endocrinol Diabetes,2003,111(1):12-15.
  • 8Small E M, Olson E N. Pervasive roles of microRNAs in cardiovascular biology[J]. Nature,2011,469(7330) :336-342.
  • 9Rottiers V, Najafi-Shoushtari S H, Kristo F, et al. MicroRNAs in metabolism and metabolic diseases[J]. Cold Spring Harb Syrup Quant Biol,2011,76(1) :225-233.
  • 10Ramirez C M, Davalos A, Goedeke L, et al. MicroRNA 758 regulates cholesterol efflux through posttranscriptional repression of ATP-binding cassette transporter A1[J]. Arterioscler Thromb Vasc Biol, 2011,31 (11) ~ 2707-2714.

共引文献816

同被引文献95

  • 1陈伶利,李杰,袁肇凯,瞿岳云.早发冠心病血瘀证的分子生物学研究现状和探讨[J].岭南心血管病杂志,2011,17(S1):55-56. 被引量:2
  • 2闫冰冰,李力.DNA甲基化与卵巢癌多药耐药及预后的关系[J].中国肿瘤生物治疗杂志,2015,22(3):281-289. 被引量:7
  • 3李杰,袁肇凯.冠心病血瘀证的病机研究[J].中西医结合心脑血管病杂志,2006,4(7):613-615. 被引量:43
  • 4Sadowski SL. Congenital cardiac disease in the newborn infant: past, present, and future[J]. Crit Care Nurs Clin North Am, 2009,21(1) ~37-48.
  • 5Dolk H, Loane M, Garne E, et al. Congenital Heart Defects in Europe Prevalence and Perinatal Mortality, 2000 to 2005 I-J]. Circulation, 2011,123 (8) : 841-849.
  • 6Derwinska K, Bartnik M, Wisniowiecka-Kowalnik B, et al. Assessment of the role of copy-number variants in 150 patients with congenital heart defects[J]. Med Wieku Rozwoj, 2012,16 (3) ~175 182.
  • 7Sebat J, Lakshmi B, Troge J, et al. Large-scale copy number polymorphism in the human genome [J]. Science, 2004, 305 (5683) : 525-528.
  • 8Ia~rate AJ, Feuk L, Rivera MN, et al. Detection of large-scale variation in the human genome[J]. Nat Genet,2004,36(9) :949- 951.
  • 9Redon R, Ishikawa S, Fitch KR, et al. Global variation in copy number in the human genome[J]. Nature,2006,444(7118) :444- 454.
  • 10Ibanez P, Bonnet A, Debarges B, et al. Causal relation between a-synuclein locus duplication as a cause of familial Parkinson's disease[J]. Lancet,2004,364(9440) :1169-1171.

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