Melatonin action on oxidative stress and tumor angiogenesis in the experimental model of hepatic carcinogenesis

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Published on Thursday, 03 October 2019

Abstract

Background: Hepatocellular carcinoma (CHC) is the most common primary liver cancer and is associated with the second lowest 5-year survival rate of all tumor types. Melatonin (Mel) is a powerful antioxidant molecule that has been demonstrated to be beneficial in various pathological conditions, including HCC.

Objective: The aim of this study was to evaluate the effect of Mel on oxidative stress and angiogenic markers in liver tissue of Wistar rats in the experimental model of hepatic carcinogenesis induced by diethylnitrosamine (DEN) and acetylaminofluorene (2-AAF). Methods: 32 male Wistar rats (150g) were divided into 4 groups: Control (CO); Control+Mel (CO+Mel); DEN and DEN+Mel. DEN (50mg/kg) was administered intraperitoneally once or twice a week, associated with a single dose of 2-AAF (100mg/kg). Mel was given in drinking water at the final concentration of 20 mg/L and the treatment was started at 12th week and continued until the end of the 19 weeks of experiment. Blood samples were collected for AST, ALT, AP, γ-GT and liver samples were used to evaluate lipid peroxidation (LPO), activity of antioxidant enzymes (CAT, GPx and GST), levels of GSH and nitric oxide levels, histological analysis and expression of proteins involved in tumor angiogenesis (VEGF, PI3K, p-Akt and eNOS).

Results: The tissue damage and the fibrogenic process present in the hepatic parenchyma were decreased as well as the levels of TBARS and the activity of GST in the group DEN+Mel when compared to DEN group. CAT activity was increased in DEN+Mel group when we compared with DEN group. The expression of VEGF, PI3K, p-Akt was decreased in DEN+Mel group while eNOS expression was increased when compared to DEN group.

Conclusion: Mel was able to minimize damage in the hepatic parenchyma, reduce LPO, modulate the activity of CAT and reduce VEGF and the PI3K/Akt pathway in a experimental model of hepatic carcinogenesis.

NOTE: This publication cites: Di Bella G., Mascia F., Gualano L., Di Bella L. - Melatonin anticancer effect: review. Int J Mol Sci. 2013;14:2410–2430.

 



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- Official Web Site: The Di Bella Method;

- The Di Bella Method (A Fixed Part - Melatonin tablets. From 30-40mg/day up to 200mg/day orally in patients with advanced stage of cancer disease and/or patients without respond to traditional treatments);

- Melatonin with adenosine solubilized in water and stabilized with glycine for oncological treatment - technical preparation, effectivity and clinical findings;

- About Melatonin - In vitro, review and in vivo publications;

- Publication: Melatonin anticancer effects: Review (from Di Bella's Foundation);

- Publication: Key aspects of melatonin physiology: 30 years of research (from Di Bella's Foundation);

- The Di Bella Method (A Fixed Part - Somatostatin, Octreotide, Sandostatin LAR, analogues and/or derivatives);

- Somatostatin in oncology, the overlooked evidences - In vitro, review and in vivo publications;

- Publication: Over-Expression of GH/GHR in Breast Cancer and Oncosuppressor Role of Somatostatin as a Physiological Inhibitor (from Di Bella's Foundation);

- Publication: The over-expression of GH/GHR in tumour tissues with respect to healthy ones confirms its oncogenic role and the consequent oncosuppressor role of its physiological inhibitor, somatostatin: a review of the literature (from Di Bella's Foundation);

- Publication: The Entrapment of Somatostatin in a Lipid Formulation: Retarded Release and Free Radical Reactivity (from Di Bella's Foundation);

- The Di Bella Method (A Fixed Part - All-Trans Retinoic Acid, Analogues and/or Derivatives - Approximately 60mg per day orally: 40mg per day Beta-Carotene/β-Carotene, 10mg per day ATRA and 10mg per day Axerophthol palmitate);

- All-Trans-Retinoic Acid (ATRA - analogues and/or derivatives) - In vitro, review and in vivo publications;

- Solution of retinoids in vitamin E in the Di Bella Method biological multitherapy;

- The Di Bella Method (A Fixed Part - Alpha tocopheryl acetate/Vitamin E, approximately 20 grams per day orally);

- Cancer and Vitamin E (analogues and/or derivatives) and cancer - In vitro, review and in vivo publications;

- The Di Bella Method (A Fixed Part - Vitamin C/Ascorbic Acid, 2–4 grams, twice a day orally);

- Beta-Carotene or β-carotene in Solution of retinoids in vitamin E in the Di Bella Method biological multitherapy;

- The Di Bella Method (A Fixed Part - Cyclophosphamide 50mg tablets and/or Hydroxyurea 500mg tablets, one or two per day);

- The Di Bella Method (A Fixed Part - Bromocriptine and/or Cabergoline);

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