Nanomedicine-mediated ferroptosis targeting strategies for synergistic cancer therapy.
Weimin YinJiao ChangJiuyuan SunTingting ZhangYuge ZhaoYong-Yong LiHaiqing DongPublished in: Journal of materials chemistry. B (2023)
Apoptosis-based treatment plays an important role in regulating the death of tumor cells ( e.g. , chemotherapy, radiotherapy, and immunotherapy). Nevertheless, cancer cells can escape surveillance from apoptosis-associated signaling by bypassing other biological pathways and thus result in considerable resistance to therapies. Significantly, ferroptosis, a newly identified type of regulated cell death that is characterized by iron-dependent and lipid peroxidation accumulation, has aroused great research interest in cancer therapy. Increasing approaches have been developed to induce ferroptosis of tumor cells, including using clinically approved drugs, experimentally used compounds, and nanomedicine formulations. More importantly, the emerging nanomedicine-based strategy has made great advances in tumor treatment because of the promising targeting efficacy and enhanced therapeutic effects. In this review, we mainly overview state-of-the-art research on nanomedicine-mediated ferroptosis targeting strategies for synergistic cancer therapies, such as immunotherapy, chemotherapy, radiotherapy, and photothermal therapy. The potential targeting mechanism of nanomedicine for ferroptosis induction was also included. Finally, the future development of nanomedicine in the field of ferroptosis-based cell death in tumor treatment will be envisioned, aiming to provide new insight for tumor treatment in the clinic.
Keyphrases
- cancer therapy
- cell death
- drug delivery
- cell cycle arrest
- locally advanced
- early stage
- public health
- radiation therapy
- squamous cell carcinoma
- endoplasmic reticulum stress
- transcription factor
- primary care
- young adults
- signaling pathway
- papillary thyroid
- combination therapy
- current status
- replacement therapy
- childhood cancer