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Experimental & Molecular Medicine ; : 419-426, 2011.
Article Dans Anglais | WPRIM | ID: wpr-102681

Résumé

Radiation is the most useful treatment modality for cancer patients. It initiates a series of signal cascades such as DNA damage response (DDR) signaling for repairing damaged DNA, arresting the cell cycle, and inducing cell death. Until now, few genes have been found to be regulated by radiation, which explains the molecular mechanisms of cellular responses to radiation. Although the transcriptional changes caused by radiation have been widely investigated, little is known about the direct evidence for the transcriptional control of DDR-related genes. Here, we examined the radiosensitivity of two non-small cell lung cancer cell lines (H460 and H1299), which have different p53 status. We monitored the time-dependent changes of 24 DDR-related gene expressions via microarray analysis. Based on the basal expression levels and temporal patterns, we further classified 24 DDR-related genes into four subgroups. Then, we also addressed the protein levels of several DDR-related genes such as TopBP1, Chk1 and Chk2, confirming the results of microarray analysis. Together, these results indicate that the expression patterns of DDR-related genes are associated with radiosensitivity and with the p53 statuses of H460 and H1299, which adds to the understanding of the complex biological responses to radiation.


Sujets)
Humains , Protéines adaptatrices de la transduction du signal/génétique , Protéines du cycle cellulaire/génétique , Lignée cellulaire tumorale , Survie cellulaire/effets des radiations , Altération de l'ADN/effets des radiations , Enzymes de réparation de l'ADN/génétique , Protéines de liaison à l'ADN/génétique , Analyse de profil d'expression de gènes , Régulation de l'expression des gènes tumoraux/effets des radiations , Tumeurs du poumon , Radiotolérance/génétique , Transduction du signal
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