Human Intestinal Organoids and Microphysiological Systems for Modeling Radiotoxicity and Assessing Radioprotective Agents.
Eloïse BougesCharlotte SegersNatalie LeysSarah LebeerJianbo ZhangFelice MastroleoPublished in: Cancers (2023)
Radiotherapy is a commonly employed treatment for colorectal cancer, yet its radiotoxicity-related impact on healthy tissues raises significant health concerns. This highlights the need to use radioprotective agents to mitigate these side effects. This review presents the current landscape of human translational radiobiology, outlining the limitations of existing models and proposing engineering solutions. We delve into radiotherapy principles, encompassing mechanisms of radiation-induced cell death and its influence on normal and cancerous colorectal cells. Furthermore, we explore the engineering aspects of microphysiological systems to represent radiotherapy-induced gastrointestinal toxicity and how to include the gut microbiota to study its role in treatment failure and success. This review ultimately highlights the main challenges and future pathways in translational research for pelvic radiotherapy-induced toxicity. This is achieved by developing a humanized in vitro model that mimics radiotherapy treatment conditions. An in vitro model should provide in-depth analyses of host-gut microbiota interactions and a deeper understanding of the underlying biological mechanisms of radioprotective food supplements. Additionally, it would be of great value if these models could produce high-throughput data using patient-derived samples to address the lack of human representability to complete clinical trials and improve patients' quality of life.
Keyphrases
- radiation induced
- early stage
- endothelial cells
- radiation therapy
- locally advanced
- clinical trial
- high throughput
- cell death
- high glucose
- healthcare
- end stage renal disease
- rectal cancer
- public health
- oxidative stress
- gene expression
- newly diagnosed
- chronic kidney disease
- mental health
- pluripotent stem cells
- signaling pathway
- patient reported outcomes
- stress induced
- health information
- current status
- patient reported
- pi k akt
- placebo controlled