2016
DOI: 10.1016/j.mrgentox.2016.05.004
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Toxic and DNA damaging effects of a functionalized fullerene in human embryonic lung fibroblasts

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Cited by 35 publications
(35 citation statements)
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“…C 60 fullerenes and their derivatives stimulate oxidative metabolism in erythrocytes and fibroblasts, malignant lymphocytes and epithelial cells, and endothelial cells and macrophages (Trpkovic et al 2012 ). Ershova et al ( 2016 ) reported about complex time-dependent changes in ROS levels in cells treated with C 60 fullerene derivatives. They differentiate between “early” (from 15 min to 3 h) and “late” (24 h) responses to C 60 fullerene exposure.…”
Section: Resultsmentioning
confidence: 99%
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“…C 60 fullerenes and their derivatives stimulate oxidative metabolism in erythrocytes and fibroblasts, malignant lymphocytes and epithelial cells, and endothelial cells and macrophages (Trpkovic et al 2012 ). Ershova et al ( 2016 ) reported about complex time-dependent changes in ROS levels in cells treated with C 60 fullerene derivatives. They differentiate between “early” (from 15 min to 3 h) and “late” (24 h) responses to C 60 fullerene exposure.…”
Section: Resultsmentioning
confidence: 99%
“…This results in a fusion between the MLLT10 (myeloid/lymphoid or mixed-lineage leukemia) gene and the Ap-3-like clathrin assembly protein PICALM (Clathrin assembly lymphoid myeloid leukemia), which is likely important for the tumorous nature of the cell line. Treatment exposure was 24 h. It suggests that the effect of nanoformulation could be mediated through the interaction with both membrane-associated and intracellular receptive structures (Ershova et al 2016 ). Intracellular ROS levels in U937 cells, as indicated by fluorescence intensity, significantly increased in response to the treatment with C 60 fullerenes and their nanocomplexes with anticancer drugs (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Non-thermal DBD plasma treatment induces oxidative stress from the diffusion of plasma-generated ROS, or from stimulation of the cell’s own ROS generating mechanisms [ 32 ], which results in decreased cell proliferation and differentiation [ 31 ], even cell death [ 29 , 30 , 32 ]. Our results show 4 min plasma exposure generated excessive ROS and increased MDA activity in dead embryos, which were mediated by decreasing cellular antioxidant activity and metabolic viability [ 20 , 33 ], and correlated with elevated NOX4 mRNA expression, which catalyzes the reduction of molecular oxygen to generate ROS [ 34 36 ]. NRF2 directly affects ROS levels by regulating the antioxidant defense systems through the induction of catabolism in SOD, CAT, GPx, and PRDX [ 26 , 28 , 37 ].…”
Section: Discussionmentioning
confidence: 99%
“…Ershova et al . 81 studied the cytotoxicity and genotoxicity of a C 60 fullerene derivative functionalized with five residues of 3-phenylpropionic acid and a chlorine atom arranged around one cyclopentadienyl unit, compound 36 (Fig. 7), in diploid human embryonic lung fibroblasts (HELFs).…”
Section: Photodynamic Therapymentioning
confidence: 99%