Circulating miRNAs as Potential Marker for Pulmonary Hypertension

被引:116
作者
Wei, Chuanyu [1 ]
Henderson, Heather [2 ]
Spradley, Christopher [2 ]
Li, Li [1 ]
Kim, Il-Kwon [1 ]
Kumar, Sandeep [1 ]
Hong, Nayeon [1 ]
Arroliga, Alejandro C. [2 ]
Gupta, Sudhiranjan [1 ]
机构
[1] Cent Texas Vet Hlth Care Syst, Scott & White, Texas A&M Hlth Sci Ctr, Div Mol Cardiol,Dept Med,Coll Med, Temple, TX USA
[2] Scott & White Mem Hosp & Clin, Temple, TX 76508 USA
来源
PLOS ONE | 2013年 / 8卷 / 05期
关键词
MYOCARDIAL-INFARCTION; MICRORNAS; PLASMA; EXPRESSION; BIOMARKERS; MECHANISM; GENOMICS; IMPACT;
D O I
10.1371/journal.pone.0064396
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MircoRNAs (miRNAs) are small non-coding RNAs that govern the gene expression and, play significant role in the pathogenesis of heart failure. The detection of miRNAs in circulation of pulmonary hypertensive (PH) human subjects remains elusive. In the current study, we determined the pattern of miRNAs of mild-to-severe human PH subjects and, compared them with the control subjects by miRNA array. Blood was obtained using fluoroscopic and waveform guided catheterization from the distal (pulmonary artery) port of the catheter. A total 40 human subjects were included in the study and, the degree of PH was determined by mean pulmonary arterial pressure. Among several miRNAs in the array, we validated 14 miRNAs and, the data were consistent with the array profile. We identified several novel downregulated miRNAs (miR-451, miR-1246) and upregulated miRNAs (miR-23b, miR-130a and miR-191) in the circulation of PH subjects. Our study showed novel set of miRNAs which are dysregulated in PH and, are directly proportional to the degree of PH. These miRNAs may be considered as potential biomarker for early detection of PH.
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页数:9
相关论文
共 41 条
[1]   Microvesicle-mediated RNA Molecule Delivery System Using Monocytes/Macrophages [J].
Akao, Yukihiro ;
Iio, Akio ;
Itoh, Tomohiro ;
Noguchi, Shunsuke ;
Itoh, Yuko ;
Ohtsuki, Yoshinori ;
Naoe, Tomoki .
MOLECULAR THERAPY, 2011, 19 (02) :395-399
[2]   The impact of microRNAs on protein output [J].
Baek, Daehyun ;
Villen, Judit ;
Shin, Chanseok ;
Camargo, Fernando D. ;
Gygi, Steven P. ;
Bartel, David P. .
NATURE, 2008, 455 (7209) :64-U38
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   A New Level of Complexity The Role of MicroRNAs in Cardiovascular Development [J].
Boettger, Thomas ;
Braun, Thomas .
CIRCULATION RESEARCH, 2012, 110 (07) :1000-1013
[5]   MicroRNA-92a Controls Angiogenesis and Functional Recovery of Ischemic Tissues in Mice [J].
Bonauer, Angelika ;
Carmona, Guillaume ;
Iwasaki, Masayoshi ;
Mione, Marina ;
Koyanagi, Masamichi ;
Fischer, Ariane ;
Burchfield, Jana ;
Fox, Henrik ;
Doebele, Carmen ;
Ohtani, Kisho ;
Chavakis, Emmanouil ;
Potente, Michael ;
Tjwa, Marc ;
Urbich, Carmen ;
Zeiher, Andreas M. ;
Dimmeler, Stefanie .
SCIENCE, 2009, 324 (5935) :1710-1713
[6]   Secreted microRNAs: a new form of intercellular communication [J].
Chen, Xi ;
Liang, Hongwei ;
Zhang, Junfeng ;
Zen, Ke ;
Zhang, Chen-Yu .
TRENDS IN CELL BIOLOGY, 2012, 22 (03) :125-132
[7]  
Chida A, 2012, CIRC J
[8]   Circulating MicroRNA-208b and MicroRNA-499 Reflect Myocardial Damage in Cardiovascular Disease [J].
Corsten, Maarten F. ;
Dennert, Robert ;
Jochems, Sylvia ;
Kuznetsova, Tatiana ;
Devaux, Yvan ;
Hofstra, Leon ;
Wagner, Daniel R. ;
Staessen, Jan A. ;
Heymans, Stephane ;
Schroen, Blanche .
CIRCULATION-CARDIOVASCULAR GENETICS, 2010, 3 (06) :499-506
[9]   Role for miR-204 in human pulmonary arterial hypertension [J].
Courboulin, Audrey ;
Paulin, Roxane ;
Giguere, Nellie J. ;
Saksouk, Nehme ;
Perreault, Tanya ;
Meloche, Jolyane ;
Paquet, Eric R. ;
Biardel, Sabrina ;
Provencher, Steeve ;
Cote, Jacques ;
Simard, Martin J. ;
Bonnet, Sebastien .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (03) :535-548
[10]   SURVIVAL IN PATIENTS WITH PRIMARY PULMONARY-HYPERTENSION - RESULTS FROM A NATIONAL PROSPECTIVE REGISTRY [J].
DALONZO, GE ;
BARST, RJ ;
AYRES, SM ;
BERGOFSKY, EH ;
BRUNDAGE, BH ;
DETRE, KM ;
FISHMAN, AP ;
GOLDRING, RM ;
GROVES, BM ;
KERNIS, JT ;
LEVY, PS ;
PIETRA, GG ;
REID, LM ;
REEVES, JT ;
RICH, S ;
VREIM, CE ;
WILLIAMS, GW ;
WU, M .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (05) :343-349