MicroRNAs and myocardial infarction

被引:37
作者
D'Alessandra, Yuri [2 ]
Pompilio, Giulio [2 ,3 ]
Capogrossi, Maurizio C. [1 ]
机构
[1] Ist Dermopat Immacolata IRCCS, Lab Patol Vascolare, I-00167 Rome, Italy
[2] Ctr Cardiol Monzino IRCCS, Lab Biol Vasc & Med Rigenerat, Milan, Italy
[3] Univ Milan, Dipartimento Sci Cardiovasc, Milan, Italy
关键词
biomarkers; miRNA; myocardial infarction; reperfusion injury; ISCHEMIA-REPERFUSION INJURY; EMBRYONIC STEM-CELLS; CARDIOVASCULAR-DISEASE; CIRCULATING MICRORNAS; DOWN-REGULATION; CARDIAC-HYPERTROPHY; TROPONIN ELEVATION; PROGENITOR CELLS; EXPRESSION; DIFFERENTIATION;
D O I
10.1097/HCO.0b013e3283522052
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review We will review the role of microRNAs (miRNAs), small noncoding RNAs with regulatory function, in myocardial infarction (MI). Specifically, we will examine the effect of MI on miRNAs' expression in the heart, the effect of MI on circulating miRNAs, which miRNAs' overexpression or downmodulation appears to have a therapeutic role in MI and which cardiac miRNAs are modulated by drugs/experimental molecules/cell transplantation strategies which have an established or potential therapeutic role in MI. Recent findings A rapidly increasing number of studies are showing that cardiac and circulating miRNAs are markedly altered in MI. These novel findings shed new light on the mechanisms that lead to MI complications, post-MI ventricular remodeling and cardiac repair. Further, recent studies show that circulating miRNAs may represent novel and sensitive biomarkers of MI and, possibly, also an intercellular signaling mechanism. Overexpression and downregulation of specific miRNAs are being evaluated as a novel approach to the treatment of MI. Finally, it appears that some established and potential MI therapies (approved drugs/experimental molecules/cell therapy interventions) may act, at least in part, via modulation of specific miRNAs. Summary Although miRNAs' role in MI is still largely uncharacterized, recent studies suggest that miRNAs may represent novel therapeutic targets and MI biomarkers.
引用
收藏
页码:228 / 235
页数:8
相关论文
共 74 条
  • [21] An Integrated Approach for Experimental Target Identification of Hypoxia-induced miR-210
    Fasanaro, Pasquale
    Greco, Simona
    Lorenzi, Maria
    Pescatori, Mario
    Brioschi, Maura
    Kulshreshtha, Ritu
    Banfi, Cristina
    Stubbs, Andrew
    Calin, George A.
    Ivan, Mircea
    Capogrossi, Maurizio C.
    Martelli, Fabio
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (50) : 35134 - 35143
  • [22] Circulating MicroRNAs Biomarkers or Mediators of Cardiovascular Diseases?
    Fichtlscherer, Stephan
    Zeiher, Andreas M.
    Dimmeler, Stefanie
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2011, 31 (11) : 2383 - 2390
  • [23] Distinct Roles of MicroRNA-1 and-499 in Ventricular Specification and Functional Maturation of Human Embryonic Stem Cell-Derived Cardiomyocytes
    Fu, Ji-Dong
    Rushing, Stephanie N.
    Lieu, Deborah K.
    Chan, Camie W.
    Kong, Chi-Wing
    Geng, Lin
    Wilson, Kitchener D.
    Chiamvimonvat, Nipavan
    Boheler, Kenneth R.
    Wu, Joseph C.
    Keller, Gordon
    Hajjar, Roger J.
    Li, Ronald A.
    [J]. PLOS ONE, 2011, 6 (11):
  • [24] Cardiospecific microRNA Plasma Levels Correlate with Troponin and Cardiac Function in Patients with ST Elevation Myocardial Infarction, Are Selectively Dependent on Renal Elimination, and Can Be Detected in Urine Samples
    Gidlof, Olof
    Andersson, Patrik
    van der Pals, Jesper
    Gotberg, Matthias
    Erlinge, David
    [J]. CARDIOLOGY, 2011, 118 (04) : 217 - 226
  • [25] MicroRNA-1 transfected embryonic stem cells enhance cardiac myocyte differentiation and inhibit apoptosis by modulating the PTEN/Akt pathway in the infarcted heart
    Glass, Carley
    Singla, Dinender K.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 301 (05): : H2038 - H2049
  • [26] ES cells overexpressing microRNA-1 attenuate apoptosis in the injured myocardium
    Glass, Carley
    Singla, Dinender K.
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2011, 357 (1-2) : 135 - 141
  • [27] ESC Guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation
    Hamm, Christian W.
    Bassand, Jean-Pierre
    Agewall, Stefan
    Bax, Jeroen
    Boersma, Eric
    Bueno, Hector
    Caso, Pio
    Dudek, Dariusz
    Gielen, Stephan
    Huber, Kurt
    Ohman, Magnus
    Petrie, Mark C.
    Sonntag, Frank
    Uva, Miguel Sousa
    Storey, Robert F.
    Wijns, William
    Zahger, Doron
    [J]. EUROPEAN HEART JOURNAL, 2011, 32 (23) : 2999 - 3054
  • [28] Role of miR-1 and miR-133a in myocardial ischemic postconditioning
    He, Bin
    Xiao, Jian
    Ren, An-Jing
    Zhang, Yu-Feng
    Zhang, Hao
    Chen, Min
    Xie, Bing
    Gao, Xiao-Gang
    Wang, Ying-Wei
    [J]. JOURNAL OF BIOMEDICAL SCIENCE, 2011, 18
  • [29] RETRACTED: Human Cardiac Stem Cell Differentiation Is Regulated by a Mircrine Mechanism (Publication with Expression of Concern. See vol. 139, 2019) (Publication with Expression of Concern. See vol. 139, 2019) (Retracted article. See vol. 139, 2019)
    Hosoda, Toru
    Zheng, Hanqiao
    Cabral-da-Silva, Mauricio
    Sanada, Fumihiro
    Ide-Iwata, Noriko
    Ogorek, Barbara
    Ferreira-Martins, Joao
    Arranto, Christian
    D'Amario, Domenico
    del Monte, Federica
    Urbanek, Konrad
    D'Alessandro, David A.
    Michler, Robert E.
    Anversa, Piero
    Rota, Marcello
    Kajstura, Jan
    Leri, Annarosa
    [J]. CIRCULATION, 2011, 123 (12) : 1287 - U100
  • [30] Novel MicroRNA Prosurvival Cocktail for Improving Engraftment and Function of Cardiac Progenitor Cell Transplantation
    Hu, Shijun
    Huang, Mei
    Nguyen, Patricia K.
    Gong, Yongquan
    Li, Zongjin
    Jia, Fangjun
    Lan, Feng
    Liu, Junwei
    Nag, Divya
    Robbins, Robert C.
    Wu, Joseph C.
    [J]. CIRCULATION, 2011, 124 (11) : S27 - S34