TY - JOUR
T1 - Gene expression profiling of biological pathway alterations by radiation exposure
AU - Lee, Kuei Fang
AU - Weng, Julia Tzu Ya
AU - Hsu, Paul Wei Che
AU - Chi, Yu Hsiang
AU - Chen, Ching Kai
AU - Liu, Ingrid Y.
AU - Chen, Yi Cheng
AU - Wu, Lawrence Shih Hsin
N1 - Publisher Copyright:
Copyright © 2014 Kuei-Fang Lee et al.
PY - 2014
Y1 - 2014
N2 - Though damage caused by radiation has been the focus of rigorous research, the mechanisms through which radiation exerts harmful effects on cells are complex and not well-understood. In particular, the influence of low dose radiation exposure on the regulation of genes and pathways remains unclear. In an attempt to investigate the molecular alterations induced by varying doses of radiation, a genome-wide expression analysis was conducted. Peripheral blood mononuclear cells were collected from five participants and each sample was subjected to 0.5 Gy, 1 Gy, 2.5 Gy, and 5Gy of cobalt 60 radiation, followed by arraybased expression profiling. Gene set enrichment analysis indicated that the immune system and cancer development pathways appeared to be the major affected targets by radiation exposure. Therefore, 1Gy radioactive exposure seemed to be a critical threshold dosage. In fact, after 1Gy radiation exposure, expression levels of several genes including FADD, TNFRSF10B, TNFRSF8, TNFRSF10A, TNFSF10, TNFSF8, CASP1, and CASP4 that are associated with carcinogenesis and metabolic disorders showed significant alterations. Our results suggest that exposure to low-dose radiation may elicit changes in metabolic and immune pathways, potentially increasing the risk of immune dysfunctions and metabolic disorders.
AB - Though damage caused by radiation has been the focus of rigorous research, the mechanisms through which radiation exerts harmful effects on cells are complex and not well-understood. In particular, the influence of low dose radiation exposure on the regulation of genes and pathways remains unclear. In an attempt to investigate the molecular alterations induced by varying doses of radiation, a genome-wide expression analysis was conducted. Peripheral blood mononuclear cells were collected from five participants and each sample was subjected to 0.5 Gy, 1 Gy, 2.5 Gy, and 5Gy of cobalt 60 radiation, followed by arraybased expression profiling. Gene set enrichment analysis indicated that the immune system and cancer development pathways appeared to be the major affected targets by radiation exposure. Therefore, 1Gy radioactive exposure seemed to be a critical threshold dosage. In fact, after 1Gy radiation exposure, expression levels of several genes including FADD, TNFRSF10B, TNFRSF8, TNFRSF10A, TNFSF10, TNFSF8, CASP1, and CASP4 that are associated with carcinogenesis and metabolic disorders showed significant alterations. Our results suggest that exposure to low-dose radiation may elicit changes in metabolic and immune pathways, potentially increasing the risk of immune dysfunctions and metabolic disorders.
UR - http://www.scopus.com/inward/record.url?scp=84924023127&partnerID=8YFLogxK
U2 - 10.1155/2014/834087
DO - 10.1155/2014/834087
M3 - 期刊論文
C2 - 25276823
AN - SCOPUS:84924023127
SN - 2314-6133
VL - 2014
JO - BioMed Research International
JF - BioMed Research International
M1 - 834087
ER -