Literature DB >> 29902094

Suppression of NRF2/ARE by convallatoxin sensitises A549 cells to 5-FU-mediated apoptosis.

June Lee1, Jong-Su Kang1, Le Ba Nam1, Ok-Kyung Yoo1, Young-Sam Keum1.   

Abstract

NF-E2-related factor 2 (NRF2) regulates transcription of phase II cytoprotective enzymes to protect normal cells against oxidative stress. However, a high level of NRF2 offers a growth advantage, chemoresistance, and radioresistance in cancer. In the present study, we have identified convallatoxin as a novel inhibitor of NRF2/ARE. Suppression of NRF2 by convallatoxin was not transcriptionally mediated, but regulated at the level of proteolysis. Convallatoxin activated GSK-3β and suppression of NRF2 by convallatoxin required the Neh6 domain. Convallatoxin sensitised A549 cells to 5-fluorouracil-mediated cell death by promoting apoptosis. Together, our results provide evidence that convallatoxin might be useful as a chemotherapeutic adjuvant due to its ability to suppress NRF2/ARE.

Entities:  

Keywords:  5-Fluorouracil (5-FU); NRF2; antioxidant response element (ARE); convallatoxin

Mesh:

Substances:

Year:  2018        PMID: 29902094     DOI: 10.1080/10715762.2018.1489132

Source DB:  PubMed          Journal:  Free Radic Res        ISSN: 1029-2470


  2 in total

1.  Convallatoxin suppresses osteosarcoma cell proliferation, migration, invasion, and enhances osteogenic differentiation by downregulating parathyroid hormone receptor 1 (PTHR1) expression and inactivating Wnt/β-catenin pathway.

Authors:  Xin Liu; Ze Geng; Xiangyong Ding; Yan Lou; Xingquan Zhang
Journal:  Bioengineered       Date:  2022-05       Impact factor: 6.832

Review 2.  Development of targeted therapy of NRF2high esophageal squamous cell carcinoma.

Authors:  Chorlada Paiboonrungruang; Emily Simpson; Zhaohui Xiong; Caizhi Huang; Jianying Li; Yahui Li; Xiaoxin Chen
Journal:  Cell Signal       Date:  2021-08-04       Impact factor: 4.850

  2 in total

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