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Identification of acetylshikonin as the novel CYP2J2 inhibitor with anti-cancer activity in HepG2 cells
- Source :
- Phytomedicine. 24:134-140
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Background Acetylshikonin is one of the biologically active compounds derived from the root of Lithospermum erythrorhizon, a medicinal plant with anti-cancer and anti-inflammation activity. Although there have been a few previous reports demonstrating that acetylshikonin exerts anti-cancer activity in vitro and in vivo, it is still not clear what is the exact molecular target protein of acetylshikonin in cancer cells. Purpose The purpose of this study is to evaluate the inhibitory effect of acetylshikonin against CYP2J2 enzyme which is predominantly expressed in human tumor tissues and carcinoma cell lines. Study design The inhibitory effect of acetylshikonin on the activities of CYP2J2-mediated metabolism were investigated using human liver microsomes (HLMs), and its cytotoxicity against human hepatoma HepG2 cells was also evaluated. Method Astemizole, a representative CYP2J2 probe substrate, was incubated in HLMs in the presence or absence of acetylshikonin. After incubation, the samples were analyzed by liquid chromatography and triple quadrupole mass spectrometry. The anti-cancer activity of acetylshikonin was evaluated on human hepatocellular carcinoma HepG2 cells. WST-1, cell counting, and colony formation assays were further adopted for the estimation of the growth rate of HepG2 cells treated with acetylshikonin. Results Acetylshikonin inhibited CYP2J2-mediated astemizole O-demethylation activity (Ki = 2.1 µM) in a noncompetitive manner. The noncompetitive inhibitory effect of acetylshikonin on CYP2J2 enzyme was also demonstrated using this 3D structure, which showed different binding location of astemizole and acetylshikonin in CYP2J2 model. It showed cytotoxic effects against human hepatoma HepG2 cells (IC50 = 2 μM). In addition, acetylshikonin treatment inhibited growth of human hepatocellular carcinoma HepG2 cells leading to apoptosis accompanied with p53, bax, and caspase3 activation as well as bcl2 down-regulation. Conclusion Taken together, our present study elucidates acetylshikonin displays the inhibitory effects against CYP2J2 in HLMs and anti-cancer activity in human hepatocellular carcinoma HepG2 cells.
- Subjects :
- 0301 basic medicine
Carcinoma, Hepatocellular
Pharmaceutical Science
Anthraquinones
Antineoplastic Agents
Apoptosis
Pharmacology
03 medical and health sciences
0302 clinical medicine
Cytochrome P-450 Enzyme System
In vivo
Drug Discovery
Humans
Enzyme Inhibitors
Cytotoxicity
IC50
Plant Extracts
Chemistry
Liver Neoplasms
Biological activity
Hep G2 Cells
In vitro
030104 developmental biology
Complementary and alternative medicine
Biochemistry
030220 oncology & carcinogenesis
Cancer cell
Microsomes, Liver
Microsome
Molecular Medicine
Phytotherapy
Subjects
Details
- ISSN :
- 09447113
- Volume :
- 24
- Database :
- OpenAIRE
- Journal :
- Phytomedicine
- Accession number :
- edsair.doi.dedup.....90cf19f97bc5eb6f39f5fdbf2b88e9a7
- Full Text :
- https://doi.org/10.1016/j.phymed.2016.12.001