2018
DOI: 10.1016/j.cbi.2017.10.028
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Facilitation of 9,10-phenanthrenequinone-elicited neuroblastoma cell apoptosis by NAD(P)H:quinone oxidoreductase 1

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Cited by 7 publications
(4 citation statements)
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“…Thus, natural 8-hydroxy-2-methoxy-1,4-naphthoquinone and 5-hydroxy-2-methoxy-1,4naphthoquinone from plant Juglans sinensis and series of synthetic 1,4-NQs derivatives exhibited significant cytotoxicity against human SH-SY5Y and mouse Neuro-2a neuroblastoma cells [21,35]. Exposure to some 1,2-NQs и 1,4-NQs provokes human neuroblastoma cell lines SK-N-SH apoptosis in a ROS-dependent pathway, including DNA damage, mitochondrial dysfunction, and resultant caspase 3 and 9 activation together with GSH decrease, proteasome inactivation and NQO1 upregulation [36]. Treatment of mouse hippocampal neuronal HT22 cells with 2,3-dimethoxy-1,4-naphthoquinone increased cytosolic and mitochondrial ROS and apoptosis, involving CHOP/GADD153 upregulation, JNK and p38 MAPK activation, Bak/Bax activation, mitochondrial membrane potential loss, caspase-9 and caspase-3 activation, PARP cleavage, nucleosomal DNA fragmentation, and intracellular GSH reduction [37].…”
Section: Discussionmentioning
confidence: 99%
“…Thus, natural 8-hydroxy-2-methoxy-1,4-naphthoquinone and 5-hydroxy-2-methoxy-1,4naphthoquinone from plant Juglans sinensis and series of synthetic 1,4-NQs derivatives exhibited significant cytotoxicity against human SH-SY5Y and mouse Neuro-2a neuroblastoma cells [21,35]. Exposure to some 1,2-NQs и 1,4-NQs provokes human neuroblastoma cell lines SK-N-SH apoptosis in a ROS-dependent pathway, including DNA damage, mitochondrial dysfunction, and resultant caspase 3 and 9 activation together with GSH decrease, proteasome inactivation and NQO1 upregulation [36]. Treatment of mouse hippocampal neuronal HT22 cells with 2,3-dimethoxy-1,4-naphthoquinone increased cytosolic and mitochondrial ROS and apoptosis, involving CHOP/GADD153 upregulation, JNK and p38 MAPK activation, Bak/Bax activation, mitochondrial membrane potential loss, caspase-9 and caspase-3 activation, PARP cleavage, nucleosomal DNA fragmentation, and intracellular GSH reduction [37].…”
Section: Discussionmentioning
confidence: 99%
“…Many studies demonstrated that PQ can cause toxicity in vivo and in vitro biological system via the redox cycling for the generation of ROS [ 42 , 46 , 47 , 50 , 72 , 78 , 82 ]. Excessive ROS is known to cause DNA damage resulting in gene mutation [ 99 103 ].…”
Section: 910-pq and Cellular Toxicitymentioning
confidence: 99%
“…Previous studies demonstrated that 9,10-PQ can elicit adverse cardiovascular effects such as alterations in vascular reactivity [ 48 , 72 , 82 , 145 147 ] and aortic ring relaxation [ 53 ]. Exposure to diesel exhaust containing 9,10-PQ was found to diminish humans forearm blood flow through endothelium-dependent and -independent mechanisms [ 148 ].…”
Section: The Role Of 910-pq In Cardiovascular Diseasementioning
confidence: 99%
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