The Involvement of Peroxiporins and Antioxidant Transcription Factors in Breast Cancer Therapy Resistance.
Lidija MilkovićMonika MlinarićIvan LučićAna Čipak GašparovićPublished in: Cancers (2023)
Breast cancer is still the leading cause of death in women of all ages. The reason for this is therapy resistance, which leads to the progression of the disease and the formation of metastases. Multidrug resistance (MDR) is a multifactorial process that leads to therapy failure. MDR involves multiple processes and many signaling pathways that support each other, making it difficult to overcome once established. Here, we discuss cellular-oxidative-stress-modulating factors focusing on transcription factors NRF2, FOXO family, and peroxiporins, as well as their possible contribution to MDR. This is significant because oxidative stress is a consequence of radiotherapy, chemotherapy, and immunotherapy, and the activation of detoxification pathways could modulate the cellular response to therapy and could support MDR. These proteins are not directly responsible for MDR, but they support the survival of cancer cells under stress conditions.
Keyphrases
- oxidative stress
- multidrug resistant
- transcription factor
- signaling pathway
- cancer therapy
- dna damage
- ischemia reperfusion injury
- induced apoptosis
- drug delivery
- locally advanced
- diabetic rats
- polycystic ovary syndrome
- metabolic syndrome
- adipose tissue
- dna binding
- pi k akt
- mesenchymal stem cells
- stem cells
- epithelial mesenchymal transition
- radiation induced
- pregnant women
- insulin resistance
- cell therapy
- breast cancer risk
- pregnancy outcomes
- rectal cancer
- childhood cancer