Tissue pO2 distributions in xenograft tumors dynamically imaged by Cherenkov-excited phosphorescence during fractionated radiation therapy.
Cao XuSrinivasa Rao AlluShudong JiangMengyu JiaJason R GunnCuiping YaoEthan P M LaRochelleJennifer R ShellPetr BruzaDavid J GladstoneLesley A JarvisJie TianSergei A VinogradovBrian W PoguePublished in: Nature communications (2020)
Hypoxia in solid tumors is thought to be an important factor in resistance to therapy, but the extreme microscopic heterogeneity of the partial pressures of oxygen (pO2) between the capillaries makes it difficult to characterize the scope of this phenomenon without invasive sampling of oxygen distributions throughout the tissue. Here we develop a non-invasive method to track spatial oxygen distributions in tumors during fractionated radiotherapy, using oxygen-dependent quenching of phosphorescence, oxygen probe Oxyphor PtG4 and the radiotherapy-induced Cherenkov light to excite and image the phosphorescence lifetimes within the tissue. Mice bearing MDA-MB-231 breast cancer and FaDu head neck cancer xenografts show different pO2 responses during each of the 5 fractions (5 Gy per fraction), delivered from a clinical linear accelerator. This study demonstrates subsurface in vivo mapping of tumor pO2 distributions with submillimeter spatial resolution, thus providing a methodology to track response of tumors to fractionated radiotherapy.
Keyphrases
- radiation therapy
- early stage
- locally advanced
- room temperature
- radiation induced
- squamous cell carcinoma
- deep learning
- climate change
- metabolic syndrome
- single cell
- cell proliferation
- endothelial cells
- machine learning
- small cell lung cancer
- adipose tissue
- high fat diet induced
- insulin resistance
- stress induced
- bone marrow
- optic nerve
- signaling pathway
- pi k akt
- ionic liquid
- neural network