부산대학교 도서관

There are 160,000 cancer patients worldwide treated with particle radiotherapy (RT). With the advent of proton, and high (FT) charge (Z) and energy (E) FIZE ionizing particle RT, the cardiovascular diseases risk estimates are uncertain. In addition, future deep space exploratory-type missions will expose humans to unknown but low doses of particle irradiation (IR). We examined molecular responses using transcriptome profiling in left ventricular murine cardiomyocytes isolated from mice that were exposed to 90 cGy, I GeV proton ([sup.1]H) and 15 cGy, 1 GeV/ nucleon iron ([sup.56]Fe) over 28 days after exposure. Unsupervised clustering analysis of gene expression segregated samples according to the IR response and time after exposure, with [sup.56]Fe-IR showing the greatest level of gene modulation. [sup.1]H-IR showed little differential transcript modulation. Network analysis categorized the major differentially expressed genes into cell cycle, oxidative responses, and transcriptional regulation functional groups. Transcriptional networks identified key nodes regulating expression. Validation of the signal transduction network by protein analysis and gel shift assay showed that particle IR clearly regulates a long-lived signaling mechanism for ERK1/2, p38 MAPK signaling and' identified NFATc4, GATA4, STAT3, and NF-[kappa]B as regulators of the response at specific time points. These data suggest that the molecular responses and gene expression to [sup.56]Fe-IR in cardiomyocytes are unique and long-lasting. Our study may have significant implications for the efforts of National Aeronautics and Space Administration to develop heart disease risk estimates for astronauts and for patients receiving conventional and particle RT via identification of specific HZE-IR molecular markers. cardiac physiology; cardiomyocyte; radiation biology; gene expression molecular signaling doi:10.1152/ajpheart.00050.2015.