Abstract

Liver disease, especially liver cancer, has become a threat facing the world. Now, antioxidant products are garnering great attention for the treatment and prevention of many diseases. S-Methyl methionine sulfonium chloride (MMSC) is a methionine derivative and is present in many vegetables and has anti-inflammatory effects and antioxidants. This is the first study aiming to investigate the antitumor activity of the MMSC. This study was carried out on 60 male Wistar albino rats (4–6 weeks old age) and divided into four groups, with the first group as normal control, second group as hepatocarcinoma induced by diethyl nitrosamine and carbon tetrachloride (DEN/CCL4) group, third group as normal rats treated with MMSC, and fourth group as hepatocellular carcinoma (HCC) induced rats treated with MMSC. Our findings revealed that MMSC administration after HCC induction significantly improved (p < 0.05) the liver function biomarkers, including AST, GGT, albumin, globulin, and albumin/globulin ratio (A/G), in comparison with those in the HCC group. Moreover, the histopathological changes of the liver tissue in the HCC group were improved by MMSC treatment. Likewise, the expression levels of tumor necrosis factor-alpha (TNF-α), induced nitric oxide synthase (iNOS), transforming growth factor (TGF-1β), and glypican 3 (GP3) were downregulated by MMSC treatment after HCC induction in comparison with those in the HCC-induced group. In conclusion, MMSC showed antitumor activity against HCC induction by DEN/CCl4 through decreasing lipid peroxide formation, the expression level of an inflammatory cytokines such as (TNF-α), immunoregulatory cytokines such as (TGF-1β), induced nitric oxide synthase, and glypican 3.

Highlights

  • Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related deaths, and the rate of HCC in men is three times higher than in women [1]

  • The antitumor activity of the S-methylmethionine sulfonium chloride was confirmed through investigation of its effect on the expression of inflammatory cytokine (TNF-α, induced nitric oxide synthase (iNOS), TGF-1β) and glypican 3 (GP3) by qRT-PCR

  • This present study has shown that the expression level of these inflammatory cytokines and GP3 was significantly up-regulated (p < 0.05)

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Summary

Introduction

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related deaths, and the rate of HCC in men is three times higher than in women [1]. In 2013, HCC acted as 4.3% of all cancer cases, and it is counted as the fourth most common cancer in men and eighth most common cancer in women [2]. There are many risk factors for HCC production such as chronic alcohol drinking, aflatoxin B1 infection, hepatitis B and C 4.0/).

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