Unearthing an unknown function of a  known vaccine in regenerative muscle atrophy: Repurposing the tuberculosis(TB) vaccine into a muscular dystrophy vaccine: BCG/TB vaccine increases the expression of IGF-1, PI3K(p85a) and B-Myb, decreases the expression of tumor suppressors, promotes regeneration of muscle cells, and reverses muscle atrophy via upregulation of its target gene, 23/July/2018, 11.49 pm

Repurposing the tuberculosis vaccine into a diabetic vaccine: TB/BCG vaccine, a tuberculosis vaccine, decreases DNA-PPK expression, suppresses phosphorylation of HSP90a, increases AMPK activity, augments mitochondrial biogenesis and energy metabolism, promotes weight loss and exercise endurance and alleviates TIIDM via down-regulation of its target gene, 23/July/2018, 11.14 am
July 23, 2018
A sweet way to lengthen lifespan: Astragalus polysaccharide, isolated from astragalus membraneous,  may  increase insulin sensitivity, slow down cardiac aging, and increase lifespan, via up-regulation of BubR1 and others genes, 23/July/2018, 11.58 pm
July 23, 2018
Show all

Introduction: What they say

A study from the Cardiac Regeneration and Ageing Lab, School of Life Science, Shanghai University, Shanghai 200444, China shows that “miR-29b contributes to multiple types of muscle atrophy.” This research paper was published, in the 25 May 2017 issue of the journal “Nature communications” [One of the best research journals in Biology with an I.F of 11.329 ], by Prof. Xiao J, Li J and others.


What we say:

On the foundation of this interesting finding, Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports that: Unearthing an unknown function of a  known vaccine in regenerative muscle atrophy: Repurposing the tuberculosis(TB) vaccine into a muscular dystrophy vaccine: BCG/TB vaccine increases the expression of IGF-1, PI3K(p85a) and B-Myb, decreases the expression of tumor suppressors, promotes regeneration of muscle cells, and reverses muscle atrophy via upregulation of its target gene from


From the significance of the study to Public health relevance:

Given: (1) that Muscular dystrophy/wasting is a degenerative disease; (2) that Muscular dystrophy/wasting also occur due to a number of pathophysiological conditions, including cancer, denervation, disuse and fasting ; (3) that there is no permanent cure for muscular dystrophy; (4)  the life-long discomfort and the medical care required to alleviate pain-associated (muscle weakness) with muscular dystrophy; and (5) the global economic cost spent for muscular dystrophy is enormous, there is an urgent need to find: (i) a way to rejuvenate muscle (satellite) stem cells that were lost in Muscular dystrophy; (ii) a cheaper alternative to the existing expensive drugs; and (iii) a side-effect-free natural product-based drug.


What is known?

Prof. Xiao’s research team members have shown that miRNA-29b:(1) promotes skeletal muscle atrophy; and (2) decreases the expression of IGF-1, PI3K(p85a) and B-Myb. While inhibition of MiR-29b expression: (i) stifles atrophy induced by dexamethasone (Dex), TNF-a and H2O2 treatment; (ii) increases phosphorylations of AKT (Ser-473), FOXO3A (Ser-253), mTOR and P70S6K; (iii) decreases expression of Foxo transcription factors; (iv) inhibits ubiquitin ligase expression; (v) suppresses protein degradation; (vi) increases protein synthesis; (vii) augments the expression of myosin isoforms, including Myh7; (vii) stimulates muscle regeneration, growth, and proliferation, suggesting that inhibition of MiR-29b expression in muscles may attenuate muscular dystrophy.


From research findings to Therapeutic opportunity:

This study suggests, first the first time, Bacillus Calmette Guerin (BCG) vaccine-based regenerative therapy, with detailed mechanistic insights, for Muscular dystrophy. BCG vaccine has been found to be useful in the treatment of tuberculosis, for more than 100 years, more recently in the treatment of autoimmune diabetes. However, the mechanism of action remains largely unknown.

BCG/TB vaccine, by increasing the expression of its target genes, it may decrease the expression of MiR-29b etc. (Fig. 1). Thereby, it may: (1) increase the expression of IGF-1, PI3K(p85a) and B-Myb; (2) increase phosphorylations of AKT (Ser-473), FOXO3A (Ser-253), mTOR and P70S6K; (3) decrease the expression of Forkhead Box O3 (FOXO3) and its downstream target genes such as MAFBX etc.; (4) promote the expression of myosin isoforms, such as Myh7; and (5) augment muscle regeneration, growth, and proliferation. Thus, BCG/TB vaccine, either alone or in combination with other drugs, may be used to treat muscular dystrophy (fig.1)

Figure 1. Mechanistic insights into how BCG/TB vaccine may aid in the treatment of muscular dystrophy. BCG/TB vaccine, by increasing the expression of its target gene, may promote regeneration of muscle cells and attenuate muscle dystrophy.

Figure 2. BCG/TB vaccine as a muscular dystrophy vaccine. BCG aids in the treatment of muscular dystrophy through induction of IGF1. 


Details of the research findings:

Idea Proposed/Formulated (with experimental evidence) by: Dr L Boominathan Ph.D.

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

Undisclosed mechanistic information: How does  BCG/TB vaccine increase the expression of IGF1 and PI3K(p85a)?

Amount: $ 500#

# Research cooperation

For purchase and payment details, you may reach us at info@genomediscovery.org


References:

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

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

Citation: Boominathan, L., Unearthing an unknown function of a  known vaccine in regenerative muscle atrophy: Repurposing the tuberculosis(TB) vaccine into a muscular dystrophy vaccine: BCG/TB vaccine increases the expression of IGF-1, PI3K(p85a) and B-Myb, decreases the expression of tumor suppressors, promotes regeneration of muscle cells, and reverses muscle atrophy via upregulation of its target gene, 23/July/2018, 11.49 pm, Genome-2-BioMedicine Discovery center (GBMD), http://genomediscovery.org

Comments are closed.