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Dying Cell Clearance and Its Impact on the Outcome of Tumor Radiotherapy

Overview
Journal Front Oncol
Specialty Oncology
Date 2012 Sep 14
PMID 22973558
Citations 93
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Abstract

The induction of tumor cell death is one of the major goals of radiotherapy and has been considered to be the central determinant of its therapeutic outcome for a long time. However, accumulating evidence suggests that the success of radiotherapy does not only derive from direct cytotoxic effects on the tumor cells alone, but instead might also depend - at least in part - on innate as well as adaptive immune responses, which can particularly target tumor cells that survive local irradiation. The clearance of dying tumor cells by phagocytic cells of the innate immune system represents a crucial step in this scenario. Dendritic cells and macrophages, which engulf, process and present dying tumor cell material to adaptive immune cells, can trigger, skew, or inhibit adaptive immune responses, respectively. In this review we summarize the current knowledge of different forms of cell death induced by ionizing radiation, the multi-step process of dying cell clearance, and its immunological consequences with special regard toward the potential exploitation of these mechanisms for the improvement of tumor radiotherapy.

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References
1.
Huynh M, Fadok V, Henson P . Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-beta1 secretion and the resolution of inflammation. J Clin Invest. 2002; 109(1):41-50. PMC: 150814. DOI: 10.1172/JCI11638. View

2.
Truman L, Ford C, Pasikowska M, Pound J, Wilkinson S, Dumitriu I . CX3CL1/fractalkine is released from apoptotic lymphocytes to stimulate macrophage chemotaxis. Blood. 2008; 112(13):5026-36. DOI: 10.1182/blood-2008-06-162404. View

3.
Eriksson D, Stigbrand T . Radiation-induced cell death mechanisms. Tumour Biol. 2010; 31(4):363-72. DOI: 10.1007/s13277-010-0042-8. View

4.
Urbonaviciute V, Furnrohr B, Meister S, Munoz L, Heyder P, De Marchis F . Induction of inflammatory and immune responses by HMGB1-nucleosome complexes: implications for the pathogenesis of SLE. J Exp Med. 2008; 205(13):3007-18. PMC: 2605236. DOI: 10.1084/jem.20081165. View

5.
Hanayama R, Tanaka M, Miwa K, Shinohara A, Iwamatsu A, Nagata S . Identification of a factor that links apoptotic cells to phagocytes. Nature. 2002; 417(6885):182-7. DOI: 10.1038/417182a. View