The Cancer Antioxidant Regulation System in Therapeutic Resistance.
Xuanhao GuChunyang MuRujia ZhengZhe ZhangQi ZhangTingbo LiangPublished in: Antioxidants (Basel, Switzerland) (2024)
Antioxidants play a pivotal role in neutralizing reactive oxygen species (ROS), which are known to induce oxidative stress. In the context of cancer development, cancer cells adeptly maintain elevated levels of both ROS and antioxidants through a process termed "redox reprogramming". This balance optimizes the proliferative influence of ROS while simultaneously reducing the potential for ROS to cause damage to the cell. In some cases, the adapted antioxidant machinery can hamper the efficacy of treatments for neoplastic diseases, representing a significant facet of the resistance mechanisms observed in cancer therapy. In this review, we outline the contribution of antioxidant systems to therapeutic resistance. We detail the fundamental constituents of these systems, encompassing the central regulatory mechanisms involving transcription factors (of particular importance is the KEAP1/NRF2 signaling axis), the molecular effectors of antioxidants, and the auxiliary systems responsible for NADPH generation. Furthermore, we present recent clinical trials based on targeted antioxidant systems for the treatment of cancer, assessing the potential as well as challenges of this strategy in cancer therapy. Additionally, we summarize the pressing issues in the field, with the aim of illuminating a path toward the emergence of novel anticancer therapeutic approaches by orchestrating redox signaling.
Keyphrases
- oxidative stress
- reactive oxygen species
- cancer therapy
- dna damage
- papillary thyroid
- clinical trial
- cell death
- squamous cell
- transcription factor
- anti inflammatory
- drug delivery
- ischemia reperfusion injury
- induced apoptosis
- squamous cell carcinoma
- lymph node metastasis
- single cell
- stem cells
- small molecule
- zika virus
- climate change
- young adults
- endoplasmic reticulum stress
- bone marrow
- mesenchymal stem cells
- study protocol
- smoking cessation
- phase iii
- heat shock protein