The Role of Epigenetics in Arterial Calcification

被引:23
作者
Wu, Shan-Shan [1 ,2 ]
Lin, Xiao [2 ]
Yuan, Ling-Qing [2 ]
Liao, Er-Yuan [2 ]
机构
[1] Pingxiang Peoples Hosp, Dept Endocrinol, Pingxiang 337000, Jiangxi, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Inst Metab & Endocrinol, Changsha 410011, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
SMOOTH-MUSCLE-CELLS; SERUM RESPONSE FACTOR; VASCULAR CALCIFICATION; HISTONE ACETYLATION; GENE-EXPRESSION; RENAL-DISEASE; OSTEOBLASTIC DIFFERENTIATION; BIOLOGICAL-ACTIVITY; CALCIFIED PLAQUE; DNA METHYLATION;
D O I
10.1155/2015/320849
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Arterial calcification is highly prevalent and correlated with cardiovascular mortality, especially in patients with ESRD or diabetes. The pathogenesis of arterial calcification is multifactorial, with both genetic and environmental factors being implicated. In recent years, several mechanisms contributing to arterial calcification have been proposed. However, these can only explain a small proportion of the variability in arterial calcification, which is a major obstacle for its prevention and management. Epigenetics has emerged as one of the most promising areas that may fill in some of the gaps in our current knowledge of the interaction between the environmental insults with gene regulation in the development of diseases. Epigenetics refers to heritable and acquired changes in gene transcription that occur independently of the DNA sequence. Well-known components of epigenetic regulation include DNA methylation, histone modifications, and microRNAs. Epigenetics research in the regulation of arterial calcification has only recently been elucidated. In this review, we will summarise recent progress in epigenetic pathways involved in arterial calcification and discuss potential therapeutic interventions based on epigenetic mechanisms.
引用
收藏
页数:8
相关论文
共 103 条
  • [1] Vascular calcification - Mechanisms and clinical ramifications
    Abedin, M
    Tintut, Y
    Demer, LL
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (07) : 1161 - 1170
  • [2] Media Calcification and Intima Calcification Are Distinct Entities in Chronic Kidney Disease
    Amann, Kerstin
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 3 (06): : 1599 - 1605
  • [3] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [4] [Anonymous], 2006, J Am Coll Cardiol, V47, pC1
  • [5] Bone Morphogenetic Protein-2 Decreases MicroRNA-30b and MicroRNA-30c to Promote Vascular Smooth Muscle Cell Calcification
    Balderman, Joshua A. F.
    Lee, Hae-Young
    Mahoney, Christopher E.
    Handy, Diane E.
    White, Kevin
    Annis, Sofia
    Lebeche, Djamel
    Hajjar, Roger J.
    Loscalzo, Joseph
    Leopold, Jane A.
    [J]. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2012, 1 (06): : e003905
  • [6] ATP-dependent nucleosomere modeling
    Becker, PB
    Hörz, W
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 : 247 - 273
  • [7] Identification of hundreds of conserved and nonconserved human microRNAs
    Bentwich, I
    Avniel, A
    Karov, Y
    Aharonov, R
    Gilad, S
    Barad, O
    Barzilai, A
    Einat, P
    Einav, U
    Meiri, E
    Sharon, E
    Spector, Y
    Bentwich, Z
    [J]. NATURE GENETICS, 2005, 37 (07) : 766 - 770
  • [8] Burke A. P., 2000, Z KARDIOLOGIE S, V89, pS49
  • [9] Modulation of smooth muscle gene expression by association of histone acetyltransferases and deacetylases with myocardin
    Cao, DS
    Wang, ZG
    Zhang, CL
    Oh, J
    Xing, WB
    Li, SJ
    Richardson, JA
    Wang, DZ
    Olson, EN
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (01) : 364 - 376
  • [10] Physical and functional interactions between the human DNMT3L protein and members of the de novo methyltransferase family
    Chen, ZX
    Mann, JR
    Hsieh, CL
    Riggs, AD
    Chédin, F
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2005, 95 (05) : 902 - 917