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Introduction: What they say:

A study from the State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian 361102, China shows that “c-Src phosphorylation and activation of hexokinase promotes tumorigenesis and metastasis.” This study was published in the 5 January 2017 issue of the journal “Nature communications”

by Prof. Li Qinxi, Jia Zhang, and others.


What we say:

On the foundation of this interesting finding, Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports that: Natural product-derived therapy for Metastatic human tumors: Gentian violet inhibits the expression of a number of enzymes in glycolytic cycle, and suppresses proliferation, migration, invasion, tumorigenesis and metastasis via up regulation of its target gene


From Significance of the study to Public health relevance:

Given that: (i) each year nearly 14 million people globally are diagnosed with cancer, and a little more than half of them will die; (ii) cancer deaths globally are expected to be doubled by 2030; (iii) cancer treatment causes the highest economic loss compared to all the known causes of death worldwide, there is an urgent need to find: (i) a way to prevent an individual from being susceptible to cancer by strengthening his/her own immune system; (ii) a cheaper alternative to the existing expensive anticancer drugs; (ii) a side-effect-free natural product-based drug; and (iii) a way to effectively treat and prevent metastatic progression and relapse of cancers.


What we infer from what they say:

Prof. Li Qinsi’s research team has recently shown that oncoprotein c-Src: (1) phosphorylates the rate limiting enzyme of the glycolysis Hexokinase-1/2 (HK1)/(HK2) at Tyr732; (2) prevents HK dimer formation; (3) increases affinity (decreases Km value for glucose) for glucose; and (4) promotes tumor survival even under poor glucose conditions. Further, they shown that HK1-Y732 phosphorylation level correlates with metastasis capability of primary cancers. Together, these findings suggest that inhibition of c-Src and its downstream target Hexokinase expression in cancer cells may prevent tumor growth.


From research findings to therapeutic opportunity :

This study suggests a natural product-derived anticancer therapy. Gentian violet has been shown to possess antibaterial, antifungal, antihelminthic, antitrypanosomal, and antiangiogenic properties (fig. 1). However, the mechanism of action is far from clear.

Gentian violet, by increasing the expression of its target genes, it may decrease the expression of c-Src and HK-1/2 (fig. 1). Thereby, it may: (i) augment HK dimer formation; (ii) increase Km value for glucose; (iii) decrease tumor survival; (iv) inhibit tumor proliferation and growth; and (v) promote tumor regression (fig.1).

price-100[easy_payment currency=”USD”]

Thus, pharmacological formulations encompassing Gentian violet  or its analogue alone or in combination with other known anticancer drugs” (fig. 1) may be used to inhibit metastatic progression of primary cancers.

Gentian violet (GV) inhibits c-Src expression

Figure 1. Mechanistic insights into how Gentian violet functions as an anticancer agent. Gentian violet, isolated from Firnged Gentian, by increasing the expression of its target genes, it may suppress the expression of c-Src and Hexokinase- 1/2 to promote tumor regression.


Details of the Research findings:

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

Amount: $100#

Undisclosed mechanistic information: How does Gentian violet decrease the expression of c-Src and HK1/2 to inhibit tumor growth?

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References:

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

Citation: Boominathan, L., Natural product-derived therapy for Metastatic human tumors: Gentian violet inhibits the expression of a number of enzymes in glycolytic cycle, and suppresses proliferation, migration, invasion, tumorigenesis and metastasis via up regulation of its target gene, 24/January/2017, 10.42 pm, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org

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