Biomedicine & Pharmacotherapy (Apr 2024)

Targeting Nrf2 to treat thyroid cancer

  • Zhongqin Gong,
  • Lingbin Xue,
  • Huangcan Li,
  • Simiao Fan,
  • Charles Andrew van Hasselt,
  • Dongcai Li,
  • Xianhai Zeng,
  • Michael Chi Fai Tong,
  • George Gong Chen

Journal volume & issue
Vol. 173
p. 116324

Abstract

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Oxidative stress (OS) is recognized as a contributing factor in the development and progression of thyroid cancer. Nuclear factor erythroid 2-related factor 2 (Nrf2) is a pivotal transcription factor involved in against OS generated by excessive reactive oxygen species (ROS). It governs the expression of a wide array of genes implicated in detoxification and antioxidant pathways. However, studies have demonstrated that the sustained activation of Nrf2 can contribute to tumor progression and drug resistance in cancers. The expression of Nrf2 was notably elevated in papillary thyroid cancer tissues compared to normal tissues, indicating that Nrf2 may play an oncogenic role in the development of papillary thyroid cancer. Nrf2 and its downstream targets are involved in the progression of thyroid cancer by impacting the prognosis and ferroptosis. Furthermore, the inhibition of Nrf2 can increase the sensitivity of target therapy in thyroid cancer. Therefore, Nrf2 appears to be a potential therapeutic target for the treatment of thyroid cancer. This review summarized current data on Nrf2 expression in thyroid cancer, discussed the function of Nrf2 in thyroid cancer, and analyzed various strategies to inhibit Nrf2.

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