Synthesis and biological evaluation of gold(III) Schiff base complexes for the treatment of hepatocellular carcinoma through attenuating TrxR activity

被引:42
作者
Bian, Mianli [1 ]
Wang, Xin [1 ]
Sun, Ying [1 ]
Liu, Wukun [1 ,2 ,3 ]
机构
[1] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Peoples R China
[2] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[3] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold(III) Schiff base complexes; Thioredoxin reductase; Reactive oxygen species; Endoplasmic reticulum stress; Hepatocellular carcinoma; HEPATIC STELLATE CELLS; THIOREDOXIN REDUCTASE; EXPERIMENTAL-MODELS; ANTICANCER AGENTS; GOLD COMPOUNDS; IN-VITRO; INHIBITION; MITOCHONDRIA; CHEMISTRY; APOPTOSIS;
D O I
10.1016/j.ejmech.2020.112234
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hepatocellular carcinoma (HCC) is one of the most common cancers and a leading cause of death worldwide. Increased thioredoxin reductase (TrxR) levels were recently identified as possible prognostic markers for HCC. Here, four gold(III) complexes 1b-4b bearing Schiff base ligands were synthesized, characterized, and screened for antitumor activity against HCC. All complexes triggered significant antiproliferative effects against HCC cells, especially the most active complex 1b induced HepG2 cells apoptosis by activating the endoplasmic reticulum stress (ERS). 1b could clearly inhibit the TrxR activity to elevate reactive oxygen species (ROS), mediate ERS and lead to mitochondrial dysfunction. Notably, treatment of 1b improved the CCl4-induced liver damage in vivo by down-regulation of TrxR expression and inflammation level. (c) 2020 Elsevier Masson SAS. All rights reserved.
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页数:14
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