Natural product-derived therapy for pulmonary fibrosis: Fla-CN, a flavonoid derivative of tiliroside, decreases miR-34 expression, increases Sirtuin-1 expression, suppresses tumor suppressor p53 acetylation, prevents apoptosis in Alveolar epithelial cell (AEC), and improves pulmonary fibrosis via down regulation of its target gene, 21/March/2017, 11.54 pm

Natural product-derived therapy for pulmonary fibrosis: Fla-CN, a flavonoid derivative of tiliroside, decreases miR-34 expression, increases Sirtuin-1 expression, suppresses tumor suppressor p53 acetylation, prevents apoptosis in Alveolar epithelial cell (AEC), and improves pulmonary fibrosis via down regulation of its target gene, 21/March/2017, 11.54 pm

Natural product-derived therapy for pulmonary fibrosis: Fla-CN, a flavonoid derivative of tiliroside, decreases miR-34 expression, increases Sirtuin-1 expression, suppresses tumor suppressor p53 acetylation, prevents apoptosis in Alveolar epithelial cell (AEC), and improves pulmonary fibrosis via down regulation of its target gene, 21/March/2017, 11.54 pm 150 150 Dr Boomi's Genom-2-Discovery Center

What we say: 

Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports that: Natural product-derived therapy for pulmonary fibrosis: Fla-CN, a  flavonoid derivative of tiliroside,  decreases miR-34 expression, increases Sirtuin-1 expression, suppresses tumor suppressor p53 acetylation, prevents apoptosis in Alveolar epithelial cell (AEC), and improves pulmonary fibrosis via down regulation of its target gene


From significance of the study to public health relevance:

Given that: (1) Idiopathic pulmonary disease (IPD)/Idiopathic pulmonary fibrosis (IPF)  is a progressive degenerative disease of the lung, with debilitating consequences; (2) drugs that are currently used to treat IPF are ineffective; and (3) 6.8-16.3 per 100,000 persons suffer from  Idiopathic pulmonary disease, there is an urgent need to find: (i) a way to induce regeneration of lung cells in pulmonary fibrosis patients; (ii) a side-effect-free natural product-based drug; and (iii) a way to effectively treat and cure PF. 


From research findings to therapeutic opportunity: 

This study suggests, for the first time, that Fla-CN, by increasing the expression of its target gene, it may: (1) decrease the expression of p53 and its target gene miR-34a; (2) increase the expression of longevity-protein Sirtuin-1; (3) suppress p53 acetylation; (4) inhibit urokinase-type plasminogen activator (uPA) and the uPA receptor expression in AECs (Alveolar epithelial cells); (5) prevent apoptosis in AECs; and (6) inhibit the development and progression of pulmonary fibrosis. Thus, pharmacological formulations encompassing “Fla-CN or its analogues either alone or in combination with other drugs“ may be used to treat pulmonary fibrosis.


Details of the research findings: 

Idea Proposed/Formulated by: Dr L Boominathan Ph.D.

Terms & Conditions apply http://genomediscovery.org/registration/terms-and-conditions/

Undisclosed mechanistic information: How Fla-CN decreases miR-34 expression to improve pulmonary fibrosis

Amount: $100#

# Research cooperation


References: 

Citation: Boominathan, L., Natural product-derived therapy for pulmonary fibrosis: Fla-CN, a  flavonoid derivative of tiliroside,  decreases miR-34 expression, increases Sirtuin-1 expression, suppresses tumor suppressor p53 acetylation, prevents apoptosis in Alveolar epithelial cell (AEC), and improves pulmonary fibrosis via down regulation of its target gene, 21/March/2017, 11.54 pm,  Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org

Web: http://genomediscovery.org or newbioideas.com

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# Research cooperation