已发表论文

NRF2在结直肠癌癌症中的双重作用:靶向NRF2作为一种潜在的治疗方法

 

Authors Hu M , Yuan L, Zhu J

Received 24 May 2024

Accepted for publication 22 August 2024

Published 4 September 2024 Volume 2024:17 Pages 5985—6004

DOI https://doi.org/10.2147/JIR.S479794

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Tara Strutt

Mengyun Hu,1 Lingling Yuan,1 Jie Zhu2 

1School of Clinical Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, People’s Republic of China; 2Hospital of Chengdu University of Traditional Chinese Medicine, Oncology Department II, Chengdu, People’s Republic of China

Correspondence: Jie Zhu, Hospital of Chengdu University of Traditional Chinese Medicine, Oncology Department II, Chengdu, 37 Shierqiao Road, Jinniu District, Chengdu City, Sichuan Province, People’s Republic of China, Tel +86 17781808796+86, Email cdzj001@sina.com

Abstract: Colorectal cancer (CRC), as the third most common bisexual cancer worldwide, requires urgent research on its underlying mechanisms and intervention methods. NRF2 is an important transcription factor involved in the regulation of redox homeostasis, protein degradation, DNA repair, and other cancer processes, playing an important role in cancer. In recent years, the complex role of NRF2 in CRC has been continuously revealed: on the one hand, it exhibits a chemopreventive effect on cancer by protecting normal cells from oxidative stress, and on the other hand, it also exhibits a protective effect on malignant cells. Therefore, this article explores the dual role of NRF2 and its related signaling pathways in CRC, including their chemical protective properties and promoting effects in the occurrence, development, metastasis, and chemotherapy resistance of CRC. In addition, this article focuses on exploring the regulation of NRF2 in CRC ferroptosis, as well as NRF2 drug modulators (activators and inhibitors) targeting CRC, including natural products, compounds, and traditional Chinese medicine formulations.

Keywords: NRF2, CRC, ferroptosis, pharmacological modulators