1. Sensitization of Patient-Derived Colorectal Cancer Organoids to Photon and Proton Radiation by Targeting DNA Damage Response Mechanisms.
- Author
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Pape, Kristin, Lößner, Anna J., William, Doreen, Czempiel, Tabea, Beyreuther, Elke, Klimova, Anna, Lehmann, Claudia, Schmäche, Tim, Merker, Sebastian R., Naumann, Max, Ada, Anne-Marlen, Baenke, Franziska, Seidlitz, Therese, Bütof, Rebecca, Dietrich, Antje, Krause, Mechthild, Weitz, Jürgen, Klink, Barbara, von Neubeck, Cläre, and Stange, Daniel E.
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COLORECTAL cancer , *PROTON therapy , *TISSUES , *COMBINED modality therapy , *DNA damage - Abstract
Simple Summary: Radiotherapy plays an important role in the treatment of colorectal cancer (CRC). Approximately one-third of patients with rectal cancer show a pathological complete response upon total neoadjuvant treatment. Patient-derived CRC organoids were investigated regarding their radiotherapeutic treatment response—both in terms of conventional photon irradiation, the combination thereof with chemotherapy, as well as proton irradiation. By inhibition of an important sensor molecule for DNA damage, which has been shown to be activated upon irradiation, radioresistant organoids could be resensitized. Pathological complete response (pCR) has been correlated with overall survival in several cancer entities including colorectal cancer. Novel total neoadjuvant treatment (TNT) in rectal cancer has achieved pathological complete response in one-third of the patients. To define better treatment options for nonresponding patients, we used patient-derived organoids (PDOs) as avatars of the patient's tumor to apply both photon- and proton-based irradiation as well as single and combined chemo(radio)therapeutic treatments. While response to photon and proton therapy was similar, PDOs revealed heterogeneous responses to irradiation and different chemotherapeutic drugs. Radiotherapeutic response of the PDOs was significantly correlated with their ability to repair irradiation-induced DNA damage. The classical combination of 5-FU and irradiation could not sensitize radioresistant tumor cells. Ataxia-telangiectasia mutated (ATM) kinase was activated upon radiation, and by inhibition of this central sensor of DNA damage, radioresistant PDOs were resensitized. The study underlined the capability of PDOs to define nonresponders to irradiation and could delineate therapeutic approaches for radioresistant patients. [ABSTRACT FROM AUTHOR]
- Published
- 2022
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