Supramolecular Nitric Oxide Depot for Hypoxic Tumor Vessel Normalization and Radiosensitization.
Cuihong YangGanen MuYing ZhangYang GaoWenxue ZhangJinjian LiuWenwen ZhangPaiyun LiLijun YangZhimou YangJie GaoJianfeng LiuPublished in: Advanced materials (Deerfield Beach, Fla.) (2022)
In cancer radiotherapy, the lack of fixed DNA damage by oxygen in hypoxic microenvironment of solid tumors often leads to severe radioresistance. Nitric oxide (NO) is a potent radiosensitizer that acts in two ways. It can directly react with the radical DNA thus fixing the damage. It also normalizes the abnormal tumor vessels, thereby increasing blood perfusion and oxygen supply. To achieve these functions, the dosage and duration of NO treatment need to be carefully controlled, otherwise it will lead to the exact opposite outcomes. However, a delivery method that fulfills both requirements is still lacking. A NO depot is designed for the control of NO releasing both over quantity and duration for hypoxic tumor vessel normalization and radiosensitization. In B16-tumor-bearing mice, the depot can provide low dosage NO continuously and release large amount of NO immediately before irradiation for a short period of time. These two modes of treatment work in synergy to reverse the radioresistance of B16 tumors more efficiently than releasing at single dosage.
Keyphrases
- nitric oxide
- dna damage
- stem cells
- oxidative stress
- early stage
- hydrogen peroxide
- type diabetes
- squamous cell carcinoma
- radiation therapy
- metabolic syndrome
- dna damage response
- early onset
- magnetic resonance
- adipose tissue
- skeletal muscle
- anti inflammatory
- cell free
- locally advanced
- quantum dots
- molecular dynamics
- squamous cell
- density functional theory
- replacement therapy
- drug induced
- circulating tumor cells