Natural product-based therapy for Hepatocelluar Carcinoma: Cirsiliol (3′,4′,5-trihydroxy-6,7-dimethoxyflavone), a flavone isolated from Achillea fragrantissima, inhibits liver cancer via down regulation of Lin28 and Igf2bp3, 2/September/2014, 10.27 am

Natural product-based therapy for Hepatocelluar Carcinoma: Cirsiliol (3′,4′,5-trihydroxy-6,7-dimethoxyflavone), a flavone isolated from Achillea fragrantissima, inhibits liver cancer via down regulation of Lin28 and Igf2bp3, 2/September/2014, 10.27 am

Natural product-based therapy for Hepatocelluar Carcinoma: Cirsiliol (3′,4′,5-trihydroxy-6,7-dimethoxyflavone), a flavone isolated from Achillea fragrantissima, inhibits liver cancer via down regulation of Lin28 and Igf2bp3, 2/September/2014, 10.27 am 150 150 Dr Boomi's Genom-2-Discovery Center

A recent study from the Children’s Research Institute, Departments of Pediatrics and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA  shows that “Lin28b Is Sufficient to Drive Liver Cancer and Necessary for Its Maintenance in Murine Models.”  This study was published in the August 11 2014 Cancer Cell (No.1 journal in basic cancer biology with an I.F of ~27.238)  by Prof Zhu H, Nguyen LH, and others.

On the foundation of this interesting finding, Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports that:  Natural product-based therapy for Hepatocelluar Carcinoma:  Cirsiliol (3′,4′,5-trihydroxy-6,7-dimethoxyflavone), a flavone isolated from Achillea fragrantissima,  inhibits liver cancer via down regulation of Lin28 and Igf2bp3. Cirsiliol, by decreasing the expression of its target gene, it may decrease tumor burden and prolong survival. Together, this study suggests that pharmacological formulations encompassing “Cirsiliol or its analogues” may be used to inhibit hepatocellular carcinoma.

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

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Citation: Boominathan, Natural product-based therapy for Hepatocelluar Carcinoma:  Cirsiliol inhibits liver cancer via down regulation of Lin28 and Igf2bp3,  2/September/2014,  10.27 am,  Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org

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