Nanoceria: an innovative strategy for cancer treatment.
Joyce L Y TangShehzahdi S MoonshiHang Thu TaPublished in: Cellular and molecular life sciences : CMLS (2023)
Nanoceria or cerium oxide nanoparticles characterised by the co-existing of Ce 3+ and Ce 4+ that allows self-regenerative, redox-responsive dual-catalytic activities, have attracted interest as an innovative approach to treating cancer. Depending on surface characteristics and immediate environment, nanoceria exerts either anti- or pro-oxidative effects which regulate reactive oxygen species (ROS) levels in biological systems. Nanoceria mimics ROS-related enzymes that protect normal cells at physiological pH from oxidative stress and induce ROS production in the slightly acidic tumour microenvironment to trigger cancer cell death. Nanoceria as nanozymes also generates molecular oxygen that relieves tumour hypoxia, leading to tumour cell sensitisation to improve therapeutic outcomes of photodynamic (PDT), photothermal (PTT) and radiation (RT), targeted and chemotherapies. Nanoceria has been engineered as a nanocarrier to improve drug delivery or in combination with other drugs to produce synergistic anti-cancer effects. Despite reported preclinical successes, there are still knowledge gaps arising from the inadequate number of studies reporting findings based on physiologically relevant disease models that accurately represent the complexities of cancer. This review discusses the dual-catalytic activities of nanoceria responding to pH and oxygen tension gradient in tumour microenvironment, highlights the recent nanoceria-based platforms reported to be feasible direct and indirect anti-cancer agents with protective effects on healthy tissues, and finally addresses the challenges in clinical translation of nanoceria based therapeutics.
Keyphrases
- cell death
- reactive oxygen species
- drug delivery
- cancer therapy
- papillary thyroid
- stem cells
- oxidative stress
- dna damage
- cell cycle arrest
- squamous cell
- cell therapy
- oxide nanoparticles
- induced apoptosis
- photodynamic therapy
- type diabetes
- lymph node metastasis
- small molecule
- squamous cell carcinoma
- skeletal muscle
- single molecule
- signaling pathway
- ischemia reperfusion injury
- adverse drug
- insulin resistance
- single cell
- bone marrow
- radiation induced
- weight loss
- radiation therapy
- energy transfer
- heat shock protein