Literature DB >> 32858502

Emerging role of NRF2 in ROS-mediated tumor chemoresistance.

Danfeng Xue1, Xiongming Zhou1, Jiaxuan Qiu2.   

Abstract

Chemoresistance is a central cause for the tumor management failure. Cancer cells disrupt the redox homeostasis through reactive oxygen species (ROS) regulatory mechanisms, leading to tumor progression and chemoresistance. The transcription factor nuclear factor erythroid 2-related factor 2 (NRF2) is a master regulator of neutralizing cellular ROS and restoring redox balance. Understanding the role of NRF2 in ROS-mediated chemoresistance can be helpful in the development of chemotherapy strategies with better efficiency. In this review, we sum up the roles of ROS in the development of chemoresistance to classical chemotherapy agents including cisplatin, 5-fluorouracil, gemcitabine, oxaliplatin, paclitaxel, and doxorubicin, and how to overcome ROS-mediated tumor chemoresistance by targeting NRF2. Finally, we propose that targeting NRF2 might be a promising strategy to resist ROS-driven chemoresistance and acquire better efficacy in cancer treatment.
Copyright © 2020 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Entities:  

Keywords:  Chemoresistance; NRF2; Reactive oxygen species

Mesh:

Substances:

Year:  2020        PMID: 32858502     DOI: 10.1016/j.biopha.2020.110676

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  14 in total

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Journal:  Cell Rep       Date:  2022-01-04       Impact factor: 9.995

4.  SLC7A11 regulated by NRF2 modulates esophageal squamous cell carcinoma radiosensitivity by inhibiting ferroptosis.

Authors:  Lei Feng; Kaikai Zhao; Liangchao Sun; Xiaoyang Yin; Junpeng Zhang; Conghe Liu; Baosheng Li
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Review 9.  Control of Oxidative Stress in Cancer Chemoresistance: Spotlight on Nrf2 Role.

Authors:  Giuseppina Barrera; Marie Angele Cucci; Margherita Grattarola; Chiara Dianzani; Giuliana Muzio; Stefania Pizzimenti
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Review 10.  Kidney cancer biomarkers and targets for therapeutics: survivin (BIRC5), XIAP, MCL-1, HIF1α, HIF2α, NRF2, MDM2, MDM4, p53, KRAS and AKT in renal cell carcinoma.

Authors:  Ieman A M Aljahdali; Renyuan Zhang; Fengzhi Li; Kent L Nastiuk; John J Krolewski; Xiang Ling
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