Fan Ruitai,Hu Yong,Liu Junqi,Zhang Jingjing,Chen Yucheng,Song Rui,Gu Hao.Effect of bortezomib on radiosensitivity of U87 glioma and distribution of cell cycle[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(08):758-760.
Fan Ruitai,Hu Yong,Liu Junqi,Zhang Jingjing,Chen Yucheng,Song Rui,Gu Hao.Effect of bortezomib on radiosensitivity of U87 glioma and distribution of cell cycle[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(08):758-760.DOI:
Effect of bortezomib on radiosensitivity of U87 glioma and distribution of cell cycle
Objective To study the effect of bortezomib (BTZ) on radiosensitivity of U87 glioma and distribution of cell cycle. Methods A nude mouse U87 glioma model was established. The nude mice were randomly divided into control group
irradiation group
BTZ group
and irradiation + BTZ group. After treatment with 8MeV-β irradiation
mice in irradiation +BTZ group were treated with BTZ by intraperitoneal injection. U87 glioma tissue was isolated and weighed. U87 glioma-inhibiting rat
e was calculated. Distribution of cell cycle
tumor growth delay (TGD) time
and sensitizing enhancement ratio (SER) were detected. The average survival time of nude mice in different groups was compared. Results The U87 glioma-inhibiting rate was significantly higher and the TGD time was significantly longer in irradiation +BTZ group than in irradiation group (46.5%vs31.5%
59 dvs38 d,P0.01). The sensitivity of radiotherapy was increased 1.44-fold when irradiation was combined with BTZ treatment. The proportion of tumor cells at the G
0
/G
1
phase was significantly lower than that of those at the G
2
/M phase after irradiation and BTZ treatment than before irradiation and BTZ treatment (79.9%vs66.0%
3.2%vs16.4%
P0.05). The survival time of nude mice was longer after irradiation and BTZ treatment. Conclusion BTZ can significantly up-regulate the radiosensitivity of U87 glioma
effectively reverse the irradiation-induced retardation of tumor cells at the G
0
/G
1
phase
increase the proportion of tumor cells at the G
2
/M phase
and prolong the survival time of tumor-bearing mice.
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