Novel miRNAs and Molecule Inhibitors to Treat PAH

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miRNAs and PAH

miRNAs and PAHNaturally occurring microRNA molecules (miRNA) hold the potential to be a new treatment for pulmonary artery disease. A group at Sookmyung University and Yale University led by Professor Kim Jong-min investigated the causes of pulmonary arterial hypertension and discovered new molecular mechanism contributing to the disease.

“Our research is meaningful in the we presented a new paradigm of treatment to target microRNA pieces that prohibit the aberrant proliferation of the pulmonary artery endothelial cells  (PAECs),” said Professor Kim in a news article.

The idea for using miRNA came from a series of experiments that revealed a significantly impaired activity of myocyte enhancer factor 2 proteins (MEF2) in PAECs extracted from pulmonary hypertension patient tissue samples. MEF2 impairment was likely causing increased proliferation of the cells, which could lead to blockages in artery walls and aggravation of disease in vivo.

In pursuit of a mechanism for MEF2 impairment, the team hypothesized two class IIa histone deacetylase proteins (HDACs) were accumulating in cell nuclei. By treating pulmonary hypertension-induced animal models with the HDAC IIa inhibitor MC1568, the researchers were able to decrease the amount of muscle in artery walls and vascular muscle cell proliferation. Accordingly, augmenting MEF2 activity may have therapeutic value in treating pulmonary arterial hypertension.

MiRNAs can be synthesized to target HDACs in patients. Alternatively, it may be possible to develop MC1568 as a therapeutic for patients. “After the MC1568 goes through tests for possible adverse effects, I think it will present a good opportunity for patients,” concluded Professor Kim.

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Maureen Newman is a science columnist for Pulmonary Hypertension News. She is currently a PhD student studying biomedical engineering at University of Rochester, working towards a career of research in biomaterials for drug delivery and regenerative medicine. She is an integral part of Dr. Danielle Benoit's laboratory, where she is investigating bone-homing therapeutics for osteoporosis treatment.
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