Modulation of Radiation responses by pre-exposure to irradiated Cell conditioned medium.
Issue Date
2007-04Keywords
HUMAN PAPILLOMA VIRUSNEOPLASMS
CANCER
RADIOTHERAPY
MeSH
Adaptation, PhysiologicalCell Line
Cell Survival
Culture Media, Conditioned
DNA
DNA Damage
Dose-Response Relationship, Radiation
Humans
Keratinocytes
Radiation Dosage
Radiation Tolerance
Metadata
Show full item recordCitation
Modulation of radiation responses by pre-exposure to irradiated cell conditioned medium. 2007, 167 (4):485-92 Radiat. Res.Publisher
Radiation Research SocietyJournal
Radiation researchDOI
10.1667/RR0159.1PubMed ID
17388689Abstract
The aim of this study was to investigate whether exposure of HPV-G cells to irradiated cell conditioned medium (ICCM) could induce an adaptive response if the cells were subsequently challenged with a higher ICCM dose. Clonogenic survival and major steps in the cascade leading to apoptosis, such as calcium influx and loss of mitochondrial membrane potential, were examined to determine whether these events could be modified by giving a priming dose of ICCM before the challenge dose. Clonogenic survival data indicated an ICCM-induced adaptive response in HPV-G cells "primed" with 5 mGy or 0.5 Gy ICCM for 24 h and then exposed to 0.5 Gy or 5 Gy ICCM. Reactive oxygen species (ROS) were found to be involved in the bystander-induced cell death. Calcium fluxes varied in magnitude across the exposed cell population, and a significant number of the primed HPV-G cells did not respond to the challenge ICCM dose. No significant loss of mitochondrial membrane potential was observed when HPV-G cells were exposed to 0.5 Gy ICCM for 24 h followed by exposure to 5 Gy ICCM for 6 h. Exposure of HPV-G cells to 5 mGy ICCM for 24 h followed by exposure to 0.5 Gy ICCM for 18 h caused a significant increase in mitochondrial mass and a change in mitochondrial location, events associated with the perpetuation of genomic instability. This study has shown that a priming dose of ICCM has the ability to induce an adaptive response in HPV-G cells subsequently exposed to a challenge dose of ICCM.Item Type
ArticleLanguage
enISSN
0033-7587ae974a485f413a2113503eed53cd6c53
10.1667/RR0159.1
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