Genome-Wide Microarray Analysis of Human Fibroblasts in Response to γ Radiation and the Radiation-Induced Bystander Effect

被引:16
作者
Kalanxhi, Erta [1 ]
Dahle, Jostein [1 ]
机构
[1] Oslo Univ Hosp, Inst Canc Res, Dept Radiat Biol, N-0310 Oslo, Norway
关键词
GENE-EXPRESSION; IONIZING-RADIATION; IRRADIATED-CELLS; ALPHA-PARTICLE; INTERCELLULAR COMMUNICATION; PHOTODYNAMIC TREATMENT; MITOCHONDRIAL-FUNCTION; TARGETED IRRADIATION; SIGNALING PATHWAY; CANCER-THERAPY;
D O I
10.1667/RR2694.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Kalanxhi, E. and Dahle, J. Genome-Wide Microarray Analysis of Human Fibroblasts in Response to gamma Radiation and the Radiation-Induced Bystander Effect. Radiat. Res. 177, 35-43 (2012). Radiation-induced bystander effects have been studied extensively due to their potential implications for cancer therapy and radiation protection; however, a complete understanding of the molecular mechanisms remains to be elucidated. In this study, we monitored transcriptional responses to gamma radiation in irradiated and bystander fibroblasts simultaneously employing a genome-wide microarray approach to determine factors that may be modulated in the generation or propagation of the bystander effect. For the microarray data we employed analysis at both the single-gene and gene-set level to place the findings in a biological context. Unirradiated bystander fibroblasts that were recipients of growth medium harvested from irradiated cultures 2 h after exposure to 2 Gy displayed transient enrichment in gene sets belonging to ribosome, oxidative phosphorylation and neurodegenerative disease pathways associated with mitochondria! dysfunctions. The response to direct irradiation was characterized by induction of signaling and apoptosis genes and the gradual formation of a cellular immune response. A set of 14 genes, many of which were regulated by p53, were found to be induced early after irradiation (prior to medium transfer) and may be important in the generation or propagation of the bystander effect. (C) 2012 by Radiation Research Society
引用
收藏
页码:35 / 43
页数:9
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