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USP22 inhibits ferroptosis. 17 / 17
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17
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"Additionally, A549 and H1975 LUAD cells with USP22 silencing exhibited a higher expression of ACSL4 and lower levels of SLC7A11 and GPX4 than sh‐Ctrl controls; however, these changes could be markedly reversed by COL17A1 reexpression (Figure 6J,K), indicating that USP22 silencing induces cell ferroptosis via COL17A1 downregulation."
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"Finally, in vivo study proved that miR-144-3p antagomir could restore the impaired function of pancreatic β-cells by suppressing ferroptosis to exert anti-hyperglycemic effect on T2DM mice.In short, the abnormal up-regulation of miR-144-3p clearly suppressed the expression of USP22 mRNA and inhibited its downstream effects on the ferroptosis pathway to cause the dysfunction of pancreatic β cells (Fig. 6), thereby promoting the progression of T2DM."
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"To prove that the upregulation of TFRC transcription mediates the promotion of ferroptosis caused by USP22 knockout, we knocked down TFRC expression through transfecting its specific small interfering RNAs (siRNAs) into USP22 knockout cells (Figure 7A), and subsequently measured cell viability, cell death, cellular lipid ROS, cellular GSH and Fe levels."