Abstract |
Hepatocellular carcinoma is one of the most common malignancies worldwide and evidence suggests that Ras signaling regulates various hallmarks of cancer via regulating several effector pathways such as ERK and PI3K. The aim of the present study is to understand the efficacy of a flavonoid myricetin for the first time in inhibiting the downstream target p21 activated kinase 1 (PAK1) of Ras signaling pathway in hepatocellular carcinoma. The analysis of gene expression revealed that myricetin inhibits PAK1 by abrogating the Ras-mediated signaling by decelerating Wnt signaling, the downstream of Erk/Akt, thereby inducing intrinsic caspase-mediated mitochondrial apoptosis by downregulating the expression of anti-apoptotic Bcl-2 and survivin and upregulating pro-apoptotic Bax. The results also provide striking evidence that the myricetin inhibits the development of HCC by inhibiting PAK1 via coordinate abrogation of MAPK/ERK and PI3K/AKT and their downstream signaling Wnt/β- catenin pathway, thus being a promising candidate for cancer prevention and therapy.
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Authors | Soumya C Iyer, Ashidha Gopal, Devaraj Halagowder |
Journal | Molecular and cellular biochemistry
(Mol Cell Biochem)
Vol. 407
Issue 1-2
Pg. 223-37
(Sep 2015)
ISSN: 1573-4919 [Electronic] Netherlands |
PMID | 26104578
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Analgesics
- Flavonoids
- myricetin
- PAK1 protein, human
- p21-Activated Kinases
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Topics |
- Analgesics
(administration & dosage, pharmacology)
- Animals
- Apoptosis
- Carcinoma, Hepatocellular
(drug therapy, enzymology, pathology)
- Cell Proliferation
(drug effects)
- Flavonoids
(administration & dosage, pharmacology)
- Gene Expression Regulation, Neoplastic
(drug effects)
- Hep G2 Cells
- Humans
- Liver Neoplasms
(drug therapy, enzymology, pathology)
- Male
- Rats
- Signal Transduction
(drug effects)
- Xenograft Model Antitumor Assays
- p21-Activated Kinases
(genetics, metabolism)
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