Molecular therapy for Metastatic cancers: Torasemide, an anti-hypertensive drug, increases the expression of tumor/metastasis suppressors CCM3/KRIT1 and TIMP3, inhibits cell cycle progression, and suppresses migration, invasion and metastasis of cancer cells via up regulation of its target gene, 8/January/2017, 10.48 pm
Lifespan extension therapy: Tomatidine, isolated from unripe tomato, among others, prolongs mammalian life span via down regulation of angiotensin II type I receptor (AT1R), 8/January/2017, 10.41 pm
January 8, 2018
Molecular therapy for Diabetic retinopathy: A pharmaceutical mixture encompassing α-lipoic acid, Epicatechin and Marine (LAEM) inhibits Soluble epoxide hydrolase (sEH) expression, decreases toxic 19,20-dihydroxydocosapentaenoic acid levels, inhibits pericyte loss, vascular permeability, and inflammation of the eye and progression of diabetic retinopathy, via down regulation of its target gene, 8/January/2018, 10.56 pm
January 8, 2018From Significance of the study to Public health relevance:
Given that: (i) each year nearly 14 million people are diagnosed with cancer globally, and little more than half of them will die; (ii) cancer deaths globally are expected to be doubled by 2030; (iii) most of the cancer patients die due to metastasis; (iv) cancer treatment causes the highest economic loss compared to all the known causes of death worldwide, there is an urgent need to find: (i) bio-molecules that drive metastatic process; and the the way to prevent their expression; (ii) a way to activate immune system to combat cancer (Cancer immunotherapy); (ii) a cheaper alternative to the existing expensive anticancer drugs; (ii) a side-effect-free natural product-based drug; (iii) increase the therapeutic index of anticancer drugs; and (iv) a way to effectively treat and prevent metastatic progression and relapse of advanced/drug-resistant cancers.
Research findings to Therapeutic opportunity:
This study suggests, for the first time, that Torasemide, by regulating the expression of its target genes, it may increase the expression of tumor suppressors CCM3/KRIT1 and TIMP3 (fig. 1).
Thereby, it may: (a) inhibit cell cycle progression; and (d) suppress migration, invasion and metastasis of cancer cells. [easy_payment currency=”USD”]
Thus, Torasemide-based treatment may be advised for metastatic cancer patients to (i) increase the expression of metastasis suppressor genes in tumors; (ii) inhibit the progression of metastatic tumors; and (ii) enhance the efficacy of Cancer therapy. Together, this study suggests that oncologists may consider experimenting Torasemide in the treatment of advanced metastatic cancers.
Details of the research findings:
Idea Proposed/Formulated (with experimental evidence) by:
Dr L Boominathan Ph.D.
Amount: $10#
Undisclosed mechanistic information: How Torasemide increases the expression of tumor/metastasis suppressors CCM3/KRIT1 and TIMP3
Fig1. Mechanistic insights into how the anti-hypertensive medication Torasemide functions as an anti-metastasis agent. Torasemide increases the expression of tumor suppressors CCM3/KRIT1 and TIMP3 via up regulation of its target genes.
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References:
Citation: Boominathan, L., Molecular therapy for Metastatic cancers: Torasemide, an anti-hypertensive drug, increases the expression of tumor/metastasis suppressors CCM3/KRIT1 and TIMP3, inhibits cell cycle progression, and suppresses migration, invasion and metastasis of cancer cells via up regulation of its target gene, 8/January/2017, 10.48 pm, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org
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