Published May 2014 | Version v1
Journal article

Synergism inhibition effect of adenovirus-mediated IL-21 gene combined with ionizing radiation on the growth of pulmonary carcinoma cells

  • 1. Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Tianjin (China)

Description

Objective: To explore the synergism inhibition effect of adenovirus-mediated inter-leukin-21(IL-21) gene combined with ionizing radiation on the growth of pulmonary carcinoma cells A549. Methods: A549 cells were divided into four groups: blank control group, Ad-IL-21 group (cells were transfected with Ad-IL-21), radiation group (cells were exposed to 6 Gy 137Cs γ-ray) and Ad-IL-21 combined with radiation group (cells were transfected with Ad-IL-21 before exposed to 6 Gy 137Cs γ-ray). The cell growth, cell cycle and cell apoptosis of A549 cells were observed. Results: The inhibition rate of Ad-IL-21 combined with radiation group was the highest, reached 40%, which was significantly higher than that of Ad-IL-21 group (about 22%) and radiation group (about 17%)(F = 45.6 and 57.5, both P < 0.05). Cells of Ad-IL-21 combined with radiation group were arrested at G2 phase (35.4%), significantly higher than that of Ad-IL-21 group (25.2%) and radiation group (17.5%)(F = 16.6 and 32.8, both P < 0.05). The cell apoptosis rate of combination group was the highest, reached 33.1% and there were significant differences compared with Ad-IL-21 group (27.8%) and radiation group (14.8%)(F = 15.9 and 41.7, both P < 0.05). Conclusion: Ad-IL-21 transfection combined with radiation shows synergism effect on the inhibition of pulmonary carcinoma cells growth. (authors)

Additional details

Publishing Information

Journal Title
International Journal of Radiation Medicine and Nuclear Medicine
Journal Volume
38
Journal Issue
3
Journal Page Range
p. 161-163
ISSN
1673-4114

Optional Information

Notes
3 figs., 8 refs.; http://dx.doi.org/10.3760/cma.j.issn.1673-4114.2014.03.005