Molecular Biology Reports

, Volume 45, Issue 6, pp 2883–2896 | Cite as

Recent research progress of microRNAs in hypertension pathogenesis, with a focus on the roles of miRNAs in pulmonary arterial hypertension

  • Chenggui MiaoEmail author
  • Jun Chang
  • Guoxue Zhang


Hypertension is the most widespread disease in the world affecting humans and imparts a significant cardiovascular and renal risk to patients, and extensive research over the past few decades has enhanced our understanding of the underlying pathogenesis of hypertension. A growing number of studies have shown that miRNAs are involved in the pathological mechanisms of hypertension. This review summarizes the current understanding of miRNA-mediated modulation of gene expression in the hypertension pathogenesis in the past few years. A systematic review of PUBMED, EMBASE and SCOPUS was conducted for studies published in the past few years. The review covers three topics: miRNAs in pulmonary arterial hypertension (PAH), miRNAs and systemic arterial hypertension (SAH), miRNAs and application in hypertension. This review summarizes the current understanding of miRNA-mediated modulation in the hypertension pathogenesis in the past few years, with especially emphasis on miRNAs in PAH. We also discussed the roles of miRNAs in SAH, and the therapeutic applications of these miRNAs will be detailed discussed in this review. Evidence suggests that miRNAs are involved in the pathological mechanisms of hypertension, and the roles of miRNAs in the hypertension pathogenesis are confirmed. We need to further investigate the regulated roles of miRNAs in the pathogenesis of hypertension and the application of miRNAs in the diagnosis and treatment of this disease in the future.


Hypertension microRNA Pulmonary arterial hypertension Systemic arterial hypertension Therapeutic application 





Pulmonary arterial hypertension


Platelet-derived growth factor receptor alpha


3′ Untranslated region


Chronic obstructive pulmonary disease


Mitochondrial calcium uniporter


Mitochondrial calcium uniporter (MCU) complex


SMAD-specific E3 ubiquitin protein ligase 1


Hypoxia-inducible factor-1α


Cyclin-dependent kinase inhibitors


Pulmonary artery endothelial cell




Hypoxia-inducible factor-1α


Cyclin-dependent kinase inhibitors


Vascular smooth muscle cells


Connective tissue growth factor


Cyclin D1


Runt-related transcription factor 2


Nitric oxide


Myocyte enhancer factor 2


Systemic arterial hypertension




mtDNA-encoded cytochrome b


Aortic vascular smooth muscle cells


Spontaneously hypertensive rats


Insulin-like growth factor 1




Carotid intima media thickness


Endothelial nitric oxide synthase


Mineralocorticoid receptor


Smooth muscle cells



This project was supported by the National Natural Science Foundation of China (No. 81302783), the Stable Talent Personnel Project of Anhui Science and Technology University (No. ZRC2014473), the Excellent talent project of Anhui Science and Technology University (No. XJYXRC201801) and the Anhui Province Key Research and Development Plan (No. 1804a0802218).

Compliance with ethical standards

Conflict of interest

The authors declare that they have no competing interests.


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Copyright information

© Springer Nature B.V. 2018

Authors and Affiliations

  1. 1.School of Life and Health ScienceAnhui Science and Technology UniversityFengyangChina
  2. 2.Fourth Affiliated HospitalAnhui Medical UniversityHefeiChina
  3. 3.State Key Laboratory of Tea Biochemistry and Biotechnology, School of Science and Technology of Tea and FoodAnhui Agricultural UniversityHefeiChina

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