2017, Number 4
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Ann Hepatol 2017; 16 (4)
Hepatoprotective Effect of Curcumin on Hepatocellular Carcinoma Through Autophagic and Apoptic Pathways
Elmansi AM, El-Karef AA, El-Shishtawy MM, Eissa LA
Language: English
References: 43
Page: 607-618
PDF size: 406.92 Kb.
ABSTRACT
Background and rationale. Microtubule-associated protein light chain 3-II (LC3-II), and Sequestosome-1 (SQSTM1) are proteins
that can be used as markers for autophagic pathway. Bcl-2 protein is reported to be inversely correlated with apoptosis. We aimed
to investigate the effects of curcumin on liver inflammation and fibrosis up to the first dysplastic stage of Hepatocellular carcinoma
(HCC) induced by Thioacetamide (TAA) in rats and to clarify the effects of curcumin on LC3-II, SQSTM1, and Bcl-2. Male
Sprague-Dawley rats were randomized into four groups: Control group, TAA group, Curcumin low-dose group, and Curcumin highdose
group. The last three groups received TAA 200 mg/kg i.p. twice weekly for 18 weeks. Oxidative stress markers as hepatic
malondialdehyde (MDA) concentration and superoxide dismutase (SOD) activity were measured by colorimetric methods. Hepatic
SQSTM1 concentration was measured by ELISA, and gene expression levels of Bcl-2, and LC3-II were measured by RT-PCR.We
also investigated the
in vitro effect of curcumin on HepG2 cells viability through MTT assay, and the involvement of autophagy in
this effect.
Results. Curcumin increased the survival percent in rats, decreased -fetoprotein (AFP) concentration, and serum aspartate
aminotransferase (AST) activity, and increased serum albumin concentration. Curcumin also significantly reduced oxidative
stress in liver, inhibited apoptosis, and induced autophagy.
In vitro, curcumin (50 µ M) decreased HepG2 cells viabilityand the concentration
of SQSTM1.
Conclusions. Curcumin leads to protection against TAA induced HCC up to the first dysplastic stage through activating
autophagic pathway and inhibiting apoptosis. Also, the antioxidant activity of curcumin almost prevents liver fibrosis.
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