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
- cancer therapy
- reactive oxygen species
- drug delivery
- papillary thyroid
- stem cells
- dna damage
- oxidative stress
- squamous cell
- cell cycle arrest
- oxide nanoparticles
- induced apoptosis
- cell therapy
- healthcare
- gene expression
- photodynamic therapy
- emergency department
- single cell
- metabolic syndrome
- type diabetes
- weight loss
- squamous cell carcinoma
- crystal structure
- lymph node metastasis
- ischemia reperfusion injury
- endoplasmic reticulum stress
- childhood cancer
- small molecule
- drug induced
- drug release
- insulin resistance
- adverse drug
- pi k akt
- energy transfer
- electronic health record
- case control