Magnesium Supplementation: Effect on the Expression of Inflammation Genes in Erlich's Tumor.
Patricia Ferrante DraghiJulio Cesar Bastos FernandesGiuliana PetriEmerson Barbosa da SilvaMatheus Moreira PerezGlaucia Raquel Luciano da VeigaBeatriz da Costa Aguiar Alves ReisFernando Luiz Affonso FonsecaPublished in: Journal of dietary supplements (2021)
Magnesium supplementation may be beneficial for cancer patients due to its action as a modulator of cell proliferation and metabolism and its anti-inflammatory effect. Tumor metabolism can influence the bioavailability and absorption of nutrients, leading to an increase in the individual's nutritional needs. In this work, the effects of supplementing different dosages of magnesium chloride in mice with solid Ehrlich's tumors were investigated by analyzing their hematological, inflammatory and anthropometric biomarkers. Three dosages of magnesium chloride (MgCl2) were administered for 28 consecutive days. Animal welfare was assessed according to the criteria stipulated by the National Center for the Replacement, Refinement, and Reduction of Animals in Research (NC3Rs). The inverted grid method was used to analyze muscle strength and fatigue. Difference in expression of the Tumor Necrosis Factor (TNF-α) and the Growth Transformation Factor (TGF-β1) genes was determined by the 2-ΔCt method. The hematological evaluation consisted of the erythrogram, white blood cell and platelet counts were used for the hematological evaluation and treatment cytotoxicity. Difference in the expression of the TNF-α and TGF-β genes showed that the group that received a high dose of magnesium had a decrease in TNF-α and RNL, an improvement in well-being with a tendency to increase muscle strength and less tumor progression according to the days of treatment. The group that received a low dosage of magnesium had a smaller tumor volume and a more controlled tumor growth according to the days. The group that received an intermediate dosage presented cytotoxicity.
Keyphrases
- poor prognosis
- rheumatoid arthritis
- high dose
- cell proliferation
- genome wide
- long non coding rna
- transforming growth factor
- magnetic resonance imaging
- low dose
- genome wide identification
- gene expression
- type diabetes
- dna methylation
- cell therapy
- epithelial mesenchymal transition
- mesenchymal stem cells
- risk assessment
- metabolic syndrome
- bone marrow
- heavy metals
- quality improvement
- physical activity
- depressive symptoms
- stem cells
- body composition
- peripheral blood
- dual energy