MicroRNAs: promising therapeutic targets for the treatment of pulmonary arterial hypertension
被引:20
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作者:
Yuan, Ke
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Stanford Univ, Dept Med, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford, CA 94305 USA
Yuan, Ke
[1
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Orcholski, Mark
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Stanford Univ, Dept Med, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford, CA 94305 USA
Orcholski, Mark
[1
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Tian, Xuefei
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Stanford Univ, Dept Med, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford, CA 94305 USA
Tian, Xuefei
[1
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Liao, Xiaobo
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Stanford Univ, Dept Med, Stanford, CA 94305 USA
Cent S Univ, Xiangya Hosp 2, Div Cardiothorac Surg, Changsha 410011, Hunan, Peoples R ChinaStanford Univ, Dept Med, Stanford, CA 94305 USA
Liao, Xiaobo
[1
,2
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Perez, Vinicio A. de Jesus
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Stanford Univ, Med Ctr, Div Pulm & Crit Care Med, Dept Med, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford, CA 94305 USA
Perez, Vinicio A. de Jesus
[3
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机构:
[1] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[2] Cent S Univ, Xiangya Hosp 2, Div Cardiothorac Surg, Changsha 410011, Hunan, Peoples R China
[3] Stanford Univ, Med Ctr, Div Pulm & Crit Care Med, Dept Med, Stanford, CA 94305 USA
Introduction: MicroRNAs (miRNAs) are small noncoding RNAs that not only regulate gene expression during normal development but can also be active players in several diseases. To date, several studies have demonstrated a possible role for specific miRNAs in the regulation of pulmonary vascular homeostasis suggesting that novel therapeutic agents which target these modulators of gene expression could serve to treat pulmonary arterial hypertension (PAH). Areas covered: The characterization of miRNA-mediated gene modulation in the pulmonary circulation is expanding very rapidly. This review summarizes current relevant findings on the role of miRNAs in the pathogenesis of PAH and expands on the potential use of agents that target these molecules as future disease-modifying therapies. Expert opinion: Further understanding of miRNA biology and function in the pulmonary circulation will serve to further enhance our understanding of their contribution to the pathogenesis of PAH. The implementation of a systems biology approach will help accelerate the discovery of miRNAs that influence angiogenesis and cellular responses to vascular injury. Experimental characterization of these miRNAs using in vitro and in vivo methods will be required to validate the biological roles of these miRNAs prior to the consideration of their use as therapeutic targets in future clinical trials.
机构:
Calif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USACalif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
Ho, Linh
Hossen, Nazir
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Calif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USACalif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
Hossen, Nazir
Nguyen, Trieu
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Calif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
East Bay Inst Res & Educ EBIRE, Mather, CA 95655 USACalif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
Nguyen, Trieu
Vo, Au
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Univ Calif Los Angeles, Dept Life Sci, Los Angeles, CA 90095 USACalif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
Vo, Au
Ahsan, Fakhrul
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Calif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USACalif Northstate Univ, Coll Pharm, Dept Pharmaceut & Biomed Sci, Elk Grove, CA 95757 USA
机构:
Univ Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, FranceUniv Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, France
Loyer, Xavier
Mallat, Ziad
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Univ Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, France
Univ Cambridge, Dept Med, Cambridge CB2 2QQ, EnglandUniv Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, France
Mallat, Ziad
Boulanger, Chantal M.
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Univ Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, FranceUniv Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, France
Boulanger, Chantal M.
Tedgui, Alain
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Univ Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, FranceUniv Paris 05, Sorbonne Paris Cite, Paris Cardiovasc Res Ctr PARCC, INSERM,UMR S 970, F-75015 Paris, France