C 60 fullerene and its nanocomplexes with anticancer drugs modulate circulating phagocyte functions and dramatically increase ROS generation in transformed monocytes
C fullerene-based nanoformulations are proposed to have a direct toxic effect on tumor cells. Previous investigations demonstrated that C fullerene used alone or being conjugated with chemotherapeutic agents possesses a potent anticancer activity. The main aim of this study was to investigate the ef...
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Published in | Cancer nanotechnology Vol. 9; no. 1; p. 8 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Austria
01.12.2018
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Subjects | |
Online Access | Get full text |
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Summary: | C
fullerene-based nanoformulations are proposed to have a direct toxic effect on tumor cells. Previous investigations demonstrated that C
fullerene used alone or being conjugated with chemotherapeutic agents possesses a potent anticancer activity. The main aim of this study was to investigate the effect of C
fullerene and its nanocomplexes with anticancer drugs on human phagocyte metabolic profile in vitro.
Analysis of the metabolic profile of phagocytes exposed to C
fullerene in vitro revealed augmented phagocytic activity and down-regulated reactive nitrogen species generation in these cells. Additionally, cytofluorimetric analysis showed that C
fullerene can exert direct cytotoxic effect on normal and transformed phagocytes through the vigorous induction of intracellular reactive oxygen species generation.
Cytotoxic action as well as the pro-oxidant effect of C
fullerene was more pronounced toward malignant phagocytes. At the same time, C
fullerenes have the ability to down-regulate the pro-oxidant effect of cisplatin on normal cells. These results indicate that C
fullerenes may influence phagocyte metabolism and have both pro-oxidant and antioxidant properties.
The antineoplastic effect of C
fullerene has been observed by direct toxic effect on tumor cells, as well as through the modulation of the functions of effector cells of antitumor immunity. |
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ISSN: | 1868-6958 |
DOI: | 10.1186/s12645-017-0034-0 |