Abstract

We demonstrated that X-ray irradiation at low doses of between 2 and 5 cGy stimulated proliferation of a normal human diploid. At low doses of between 2 and 5 cGy, ERK1/2 was phosphorylated as efficiently as at higher doses between 50 and 100 cGy of X-rays, while the p53 protein level was not increased by doses below 50 cGy. On the other hand, the p53 protein was efficiently accumulated at higher doses of X-ray more than 100 cGy. ERK1/2 was phosphorylated by doses over 50 cGy with increasing doses. We found that activated ERK1/2 augmented phosphorylation of the Elk-1 protein. Furthermore, over expression of ERK2 in NCI-H1299, and human lung carcinoma cells, potentiated enhanced proliferation, while down-regulation of ERK2 using the anti-sense ERK2 gene abrogated the stimulative effect of low-dose irradiation. These results indicate that a limited range of low-dose ionizing radiation differentially activate ERK1/2 kinases, which causes enhanced proliferation of cells receiving very low doses of ionizing radiation.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.