SIRT6 as a key event linking P53 and NRF2 counteracts APAP-induced hepatotoxicity through inhibiting oxidative stress and promoting hepatocyte proliferation.
作者:
关键词
AAV, adeno-associated virusALF, acute liver failureALT, serum alanine aminotransferaseAPAP, acetaminophenARE, antioxidant response elementAST, aspartate aminotransferaseAcetaminophenBCA, bicinchoninic acidBrdU, bromodeoxyuridineCCK-8, cell counting kit-8CCNA1, cyclin A1CCND1, cyclin D1CDK4, cyclin-dependent kinase 4CYP450, cytochromes P450Co-IP, co-immunoprecipitationDCF, dichlorofluoresceinDox, doxorubicinECL, electrochemiluminescenceGSH, glutathioneGSTα, glutathianone S-transferase αGSTμ, glutathione S-transferase μH&E, hematoxylin and eosinH3K56ac, histone H3 Nε-acetyl-lysines 56H3K9ac, histone H3 Nε-acetyl-lysines 9HO-1, heme oxygenase-1HepatotoxicityKEAP1, Kelch-like ECH-associated protein 1LDH, lactate dehydrogenaseNAPQI, N-acetyl p-benzoquinone imineNQO1, NAD(P)H quinone dehydrogenase 1NRF2NRF2, nuclear factor erythroid 2-related factor 2P53ROS, reactive oxygen speciesSIRT6SIRT6, sirtuin 6siRNA, small interfering RNA
DOI
10.1016/j.apsb.2020.06.016
PMID
33532182
发布时间
2021-02-06
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Acta pharmaceutica Sinica. B
2021年11卷1期
89-99页
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