Abstract

This study aimed to synthesise C60–DOX complexes followed by the analysis of their effect on the concentration of metallothionein (MT) as a non-enzymatic antioxidant and on the concentration and activity of superoxide dismutase (SOD) as an antioxidant enzyme in healthy human mammary MCF-10A cells. Dynamic light scattering and electrophoretic light scattering were used to establish the size and zeta potential of the complexes. The MT and SOD concentrations were determined using the ELISA method; SOD activity was determined by tetrazolium salt reduction inhibition. Lower MT concentration following exposure of cells to both DOX and C60 fullerene compared to the control sample was found. However, the concentration of this protein increased as a consequence of the C60–DOX complexes action on MCF-10A cells compared to the control. C60 used alone did not affect the concentration and activity of SOD in MCF-10A cells. Application of free DOX did not activate cellular antioxidant defence in the form of an increase in SOD concentration or its activity. In contrast treatment of cells with the C60–DOX complex resulted in a decrease in SOD1 concentration and a significant increase in SOD activity compared to cells treated with free DOX, C60 and control. Thus, it was found that C60–DOX complexes showed potential for protective effects against DOX-induced toxicity to MCF-10A cells.

Highlights

  • IntroductionLower MT concentration following exposure of cells to both DOX and C60 fullerene compared to the control sample was found

  • We investigated the effect of the application of C60 –DOX complexes on superoxide dismutase (SOD) level and activity in MCF-10A cells

  • The use of C60 in DOX therapy affects the efficiency of the antioxidant system in noncancerous cells

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Summary

Introduction

Lower MT concentration following exposure of cells to both DOX and C60 fullerene compared to the control sample was found. C60 –DOX complexes action on MCF-10A cells compared to the control. C60 used alone did not affect the concentration and activity of SOD in MCF-10A cells. In contrast treatment of cells with the C60 –DOX complex resulted in a decrease in SOD1 concentration and a significant increase in SOD activity compared to cells treated with free DOX, C60 and control. It was found that C60 –DOX complexes showed potential for protective effects against DOX-induced toxicity to MCF-10A cells. Treatment plans based on anthracycline antibiotics belong to the most effective therapies for breast cancer, which is the leading cause of death among women affected by cancer worldwide [4]

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