2015
DOI: 10.1016/j.chemosphere.2015.08.031
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Benzo-α-pyrene induced oxidative stress in Caenorhabditis elegans and the potential involvements of microRNA

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Cited by 28 publications
(13 citation statements)
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“…In murine X-linked muscular dystrophy (mdx) mice, a immunity relevant enzyme, glucose-6-phosphate dehydrogenase, was targeted by miR-1 in response to oxidative stress (Cacchiarelli et al, 2010). In Caenorhabditis elegans, miR-1 was involved in the oxidative stress response induced by benzo-a-pyrene (Wu et al, 2015). From this point of view, our findings concerning the targeting and regulating relationship between tci-miR-1-3p and TCGSTM4 suggest another possibility: that tci-miR-1-3p may participate in antioxidative regulation in T. cinnabarinus.…”
Section: Discussionmentioning
confidence: 99%
“…In murine X-linked muscular dystrophy (mdx) mice, a immunity relevant enzyme, glucose-6-phosphate dehydrogenase, was targeted by miR-1 in response to oxidative stress (Cacchiarelli et al, 2010). In Caenorhabditis elegans, miR-1 was involved in the oxidative stress response induced by benzo-a-pyrene (Wu et al, 2015). From this point of view, our findings concerning the targeting and regulating relationship between tci-miR-1-3p and TCGSTM4 suggest another possibility: that tci-miR-1-3p may participate in antioxidative regulation in T. cinnabarinus.…”
Section: Discussionmentioning
confidence: 99%
“…These results mirrored expression found in kidneys of elderly mice. In a study that used benzo-α-pyrene to induce oxidative stress in C. elegans , miR-1, miR-355, miR-50, miR-51, miR-58, miR-796, and miR-84 were found to have modified expression (Wu et al, 2015). These miRNAs may be involved in the regulation of SKiNhead-1, a transcription factor involved in antioxidant response element (ARE) regulation, and gamma-glutamine cysteine synthase heavy chain, an ARE (Wu et al, 2015).…”
Section: Mirna Synthesis/actionmentioning
confidence: 99%
“…In a study that used benzo-α-pyrene to induce oxidative stress in C. elegans , miR-1, miR-355, miR-50, miR-51, miR-58, miR-796, and miR-84 were found to have modified expression (Wu et al, 2015). These miRNAs may be involved in the regulation of SKiNhead-1, a transcription factor involved in antioxidant response element (ARE) regulation, and gamma-glutamine cysteine synthase heavy chain, an ARE (Wu et al, 2015). In a mouse model with oxidative liver injury induced by treatment with the anti-tuberclosis drug isoniazid, expression of miR-122 in tissue was significantly changed at days 3 and 5 (Wu et al, 2015).…”
Section: Mirna Synthesis/actionmentioning
confidence: 99%
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“…miRNAs target many crucial genes and processes that are related to ageing and cellular senescence, including oxidative stress, mitochondrial dysfunction, tumor suppression, neurodegenerative diseases, DNA damage and telomere shortening, which makes miRNA a useful tool as biomarkers of ageing and ageing-related diseases (see reviews in Harries 2014; Williams et al 2017). For instance, miR-1 is implicated in oxidative stress and neurodegenerative diseases, and miR-34a regulates mitochondria dysfunction, tumor suppression and telomere shortening, all of which somehow contribute to the ageing process (Yamakuchi et al 2008;Yang et al 2013;Wu et al 2015). miRNA can be used as a biomarker and a pool of miRNA can be used as mediator of the ageing process.…”
Section: Mirna Functionmentioning
confidence: 99%