Restoration of FGF receptor type 2 enhances radiosensitivity of hormone-refractory human prostate carcinoma PC-3 cells

被引:0
|
作者
Matsubara, Akio [1 ]
Teishima, Jun
Mirkhat, Suichinov
Yasumoto, Hiroaki
Mochizuki, Hideki [2 ]
Seki, Mitsuhiro [3 ]
Mutaguchi, Kazuaki
Mckeehan, Wallace L. [4 ]
Usui, Tsuguru
机构
[1] Hiroshima Univ, Dept Urol, Grad Sch Biomed Sci, Minami Ku, Hiroshima 7348551, Japan
[2] JA Hiroshima Kouseiren Hosp, Dept Urol, Hatsukaichi, Hiroshima, Japan
[3] Chuden Hosp, Dept Urol, Hiroshima, Japan
[4] Texas A&M Hlth Sci Ctr, Inst Biosci & Technol, Ctr Canc & Stem Cell Biol, Houston, TX USA
关键词
cell death therapy; differentiation therapy; gene therapy; prostate cancer; radiosensitivity; tumor suppression; tyrosine kinases;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study was undertaken to investigate the radiosensitizing effects of fibroblast growth factor receptor 2IIIb (FGFR2IIIb) in androgen-independent human prostate carcinoma PC-3 cells devoid of normally resident epithelial cell FGFR2IIIb. Materials and Methods: A clonal line of PC-3 cells expressing FGFR2IIIb was established by stable transfection. Clonogenic cell survival, apoptosis and cell cycle distribution with and without gamma-irradiation were then compared between FGFR2IIIb-expressing PC-3 cells and control cells mock-transfected with vector alone. Results: Gamma-irradiation resulted in an increase of clonogenic cell death concurrent with enhanced apoptosis and cell cycle arrest in the G2/M-phase in both transfected and untransfected cells. A quantitative analysis of all three parameters indicated that cells expressing FGFR2IIIb were significantly more sensitive to irradiation than control cells. Conclusion: These results indicate that restoration of FGFR2IIIb to PC-3 cells enhances their sensitivity to irradiation through acceleration of apoptosis and cell cycle arrest.
引用
收藏
页码:2141 / 2146
页数:6
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