Membrane Signaling Induced by High Doses of Ionizing Radiation in the Endothelial Compartment. Relevance in Radiation Toxicity

被引:57
作者
Corre, Isabelle [1 ]
Guillonneau, Maeva [1 ]
Paris, Francois [1 ]
机构
[1] Univ Nantes, CNRS 6299, Inst Rech Sante, CRCNA,UMR Inserm U892, F-44007 Nantes, France
关键词
radiotherapy; radiation toxicity; endothelium; plasma membrane; acid sphingomyelinase; ceramide; ACID SPHINGOMYELINASE GENE; CERAMIDE-INDUCED APOPTOSIS; KINASE-C-ZETA; NORMAL TISSUE; OXIDATIVE STRESS; LYSOSOME FUSION; GROWTH-FACTOR; DOUBLE-BLIND; CATHEPSIN-D; CELL-DEATH;
D O I
10.3390/ijms141122678
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor areas can now be very precisely delimited thanks to technical progress in imaging and ballistics. This has also led to the development of novel radiotherapy protocols, delivering higher doses of ionizing radiation directly to cancer cells. Despite this, radiation toxicity in healthy tissue remains a major issue, particularly with dose-escalation in these new protocols. Acute and late tissue damage following irradiation have both been linked to the endothelium irrigating normal tissues. The molecular mechanisms involved in the endothelial response to high doses of radiation are associated with signaling from the plasma membrane, mainly via the acid sphingomyelinase/ceramide pathway. This review describes this signaling pathway and discusses the relevance of targeting endothelial signaling to protect healthy tissues from the deleterious effects of high doses of radiation.
引用
收藏
页码:22678 / 22696
页数:19
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