Variable p53/Nrf2 crosstalk contributes to triptolide-induced hepatotoxic process.
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T. Du | Wenqun Li | Weida Wang | Xiaoguang Chen | M. Ji | M. Yan | Bi-kui Zhang | Zhen-yan Hou | H. Gong | Shan-shan Wei | Lin Guo | Huixiang Li | Mingjin Wang | Shen You
[1] Xiaoxv Dong,et al. Ginsenoside Rb1 Attenuates Triptolide-Induced Cytotoxicity in HL-7702 Cells via the Activation of Keap1/Nrf2/ARE Pathway , 2022, Frontiers in Pharmacology.
[2] J. York,et al. Inhibition of p53 sulfoconjugation prevents oxidative hepatotoxicity and acute liver failure. , 2021, Gastroenterology.
[3] M. Yan,et al. Role of MicroRNA-155 in Triptolide-induced hepatotoxicity via the Nrf2-Dependent pathway. , 2021, Journal of ethnopharmacology.
[4] Wenzhou Li,et al. SIRT6 as a key event linking P53 and NRF2 counteracts APAP-induced hepatotoxicity through inhibiting oxidative stress and promoting hepatocyte proliferation , 2020, Acta pharmaceutica Sinica. B.
[5] X. Pei,et al. Olaquindox-Induced Liver Damage Involved the Crosstalk of Oxidative Stress and p53 In Vivo and In Vitro , 2020, Oxidative medicine and cellular longevity.
[6] X. Pei,et al. Molecular mechanism of olaquindox-induced hepatotoxicity and the hepatic protective role of curcumin. , 2020, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
[7] Dasheng Lu,et al. Comprehensive analysis of transcriptomics and metabolomics to understand triptolide-induced liver injury in mice. , 2020, Toxicology letters.
[8] A. Garufi,et al. A ruthenium(II)-curcumin compound modulates NRF2 expression balancing the cancer cell death/survival outcome according to p53 status , 2020, Journal of experimental & clinical cancer research : CR.
[9] M. Schwarz,et al. Regulation of expression of drug-metabolizing enzymes by oncogenic signaling pathways in liver tumors: a review , 2019, Acta pharmaceutica Sinica. B.
[10] Weixia Sun,et al. P53/NRF2 mediates SIRT1's protective effect on diabetic nephropathy. , 2019, Biochimica et biophysica acta. Molecular cell research.
[11] Ming Yan,et al. Incidence and Etiology of Drug-Induced Liver Injury in Mainland China. , 2019, Gastroenterology.
[12] H. Cai,et al. Nrf2 participates in mechanisms for reducing the toxicity and enhancing the antitumour effect of Radix Tripterygium wilfordii to S180-bearing mice by herbal-processing technology , 2019, Pharmaceutical biology.
[13] Meilin Liu,et al. Preclinical Pharmacokinetics of Triptolide: A Potential Antitumor Drug. , 2019, Current drug metabolism.
[14] Xiaoxv Dong,et al. Triptolide Induces Apoptosis Through Fas Death and Mitochondrial Pathways in HepaRG Cell Line , 2018, Front. Pharmacol..
[15] F. Shen,et al. Triptolide induces p53‐dependent cardiotoxicity through mitochondrial membrane permeabilization in cardiomyocytes , 2018, Toxicology and applied pharmacology.
[16] Xin He,et al. Pharmacokinetic and Toxicological Characteristics of Tripterigium Glycosides and Their Derivatives. , 2018, Current drug metabolism.
[17] H. Bi,et al. p53 attenuates acetaminophen-induced hepatotoxicity by regulating drug-metabolizing enzymes and transporter expression , 2018, Cell Death & Disease.
[18] Yongbo Peng,et al. Mechanisms of Triptolide-Induced Hepatotoxicity and Protective Effect of Combined Use of Isoliquiritigenin: Possible Roles of Nrf2 and Hepatic Transporters , 2018, Front. Pharmacol..
[19] Zhen-Ning Lu,et al. DHPAC, a novel synthetic microtubule destabilizing agent, possess high anti-tumor activity in vincristine-resistant oral epidermoid carcinoma in vitro and in vivo. , 2017, The international journal of biochemistry & cell biology.
[20] Jianming Xu,et al. Rifampicin-induced injury in HepG2 cells is alleviated by TUDCA via increasing bile acid transporters expression and enhancing the Nrf2-mediated adaptive response. , 2017, Free Radical Biology & Medicine.
[21] W. Gu,et al. NRF2 Is a Major Target of ARF in p53-Independent Tumor Suppression. , 2017, Molecular cell.
[22] M. Yan,et al. The Ethanol Extract of Licorice (Glycyrrhiza uralensis) Protects against Triptolide-Induced Oxidative Stress through Activation of Nrf2 , 2017, Evidence-based complementary and alternative medicine : eCAM.
[23] Xueping Zhou,et al. Self-protection against triptolide-induced toxicity in human hepatic cells via Nrf2-ARE-NQO1 pathway , 2017, Chinese Journal of Integrative Medicine.
[24] B. Water,et al. Comprehensive Landscape of Nrf2 and p53 Pathway Activation Dynamics by Oxidative Stress and DNA Damage. , 2017, Chemical research in toxicology.
[25] Jie Zhou,et al. Toxicity of triptolide and the molecular mechanisms involved. , 2017, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[26] M. Huang,et al. Activation of Nrf2 Protects against Triptolide-Induced Hepatotoxicity , 2014, PloS one.
[27] Shu-yu Yang,et al. Comparison of toxicokinetic and tissue distribution of triptolide-loaded solid lipid nanoparticles vs free triptolide in rats. , 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[28] M. Huang,et al. Role of Nrf2 in protection against triptolide-induced toxicity in rat kidney cells. , 2012, Toxicology letters.
[29] Z. Miao,et al. Triptolide: structural modifications, structure-activity relationships, bioactivities, clinical development and mechanisms. , 2012, Natural product reports.
[30] M. Kwak,et al. Transcription factor Nrf2 maintains the basal expression of Mdm2: An implication of the regulation of p53 signaling by Nrf2. , 2011, Archives of biochemistry and biophysics.
[31] Curtis D. Klaassen,et al. Nrf2 the rescue: effects of the antioxidative/electrophilic response on the liver. , 2010, Toxicology and applied pharmacology.
[32] Curtis D. Klaassen,et al. Xenobiotic, Bile Acid, and Cholesterol Transporters: Function and Regulation , 2010, Pharmacological Reviews.
[33] M. Toledano,et al. The guardian recruits cops: the p53-p21 axis delegates prosurvival duties to the Keap1-Nrf2 stress pathway. , 2009, Molecular cell.
[34] T. Russo,et al. p53 Suppresses the Nrf2-dependent Transcription of Antioxidant Response Genes* , 2006, Journal of Biological Chemistry.
[35] P. Chumakov,et al. The antioxidant function of the p53 tumor suppressor , 2005, Nature Medicine.
[36] Y. Shaul,et al. A mechanism of ubiquitin-independent proteasomal degradation of the tumor suppressors p53 and p73. , 2005, Genes & development.
[37] J. Lotem,et al. Mdm-2 and ubiquitin-independent p53 proteasomal degradation regulated by NQO1 , 2002, Proceedings of the National Academy of Sciences of the United States of America.