Frey B, Derer A, Scheithauer H, Wunderlich R, Fietkau R, Gaipl U (2016)
Publication Type: Journal article
Publication year: 2016
Book Volume: 930
Pages Range: 151-72
DOI: 10.1007/978-3-319-39406-0_7
Radiotherapy (RT) predominantly is aimed to induce DNA damage in tumour cells that results in reduction of their clonogenicity and finally in tumour cell death. Adaptation of RT with higher single doses has become necessary and led to a more detailed view on what kind of tumour cell death is induced and which immunological consequences result from it. RT is capable of rendering tumour cells immunogenic by modifying the tumour cell phenotype and the microenvironment. Danger signals are released as well as the senescence-associated secretory phenotype. This results in maturation of dendritic cells and priming of cytotoxic T cells as well as in activation of natural killer cells. However, RT on the other hand can also result in immune suppressive events including apoptosis induction and foster tumour cell proliferation. That's why RT is nowadays increasingly combined with selected immunotherapies.
APA:
Frey, B., Derer, A., Scheithauer, H., Wunderlich, R., Fietkau, R., & Gaipl, U. (2016). Cancer Cell Death-Inducing Radiotherapy: Impact on Local Tumour Control, Tumour Cell Proliferation and Induction of Systemic Anti-tumour Immunity. Advances in Experimental Medicine and Biology, 930, 151-72. https://doi.org/10.1007/978-3-319-39406-0_7
MLA:
Frey, Benjamin, et al. "Cancer Cell Death-Inducing Radiotherapy: Impact on Local Tumour Control, Tumour Cell Proliferation and Induction of Systemic Anti-tumour Immunity." Advances in Experimental Medicine and Biology 930 (2016): 151-72.
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