Heavy-ion Radiobiology Research Group, National Institute of Radiological Sciences, Chiba, Japan.
Cancer Sci. 2011 Jun;102(6):1176-80. doi: 10.1111/j.1349-7006.2011.01916.x. Epub 2011 Apr 4.
ZSTK474 is a novel orally applicable phosphoinositide 3-kinase-specific inhibitor that strongly inhibits cancer cell proliferation. To further explore the antitumor effect of ZSTK474 for future clinical usage, we studied its combined effects with radiation. The proliferation of HeLa cells was inhibited by treatment with X-rays alone or ZSTK474 alone. Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 24 h post-irradiation, significantly enhanced cell growth inhibition. The combined effect was also observed for clonogenic survival with continuous ZSTK474 treatment. Western blot analysis showed enhanced phosphorylation of Akt and GSK-3β by X-irradiation, whereas phosphorylation was inhibited by ZSTK474 treatment alone. Treatment with ZSTK474 after X-irradiation also inhibited phosphorylation, and remarkably inhibited xenograft tumor growth. Combined treatment with X-rays and ZSTK474 has greater therapeutic potential than radiation or drug therapy alone, both in vitro and in vivo.
ZSTK474 是一种新型的口服应用的磷酸肌醇 3-激酶特异性抑制剂,能强烈抑制癌细胞增殖。为了进一步探索 ZSTK474 的抗肿瘤作用,以应用于未来的临床治疗,我们研究了其与放疗的联合作用。单独使用 X 射线或 ZSTK474 处理均可抑制 HeLa 细胞的增殖。从照射后 24 小时开始,连续 8 天口服给予 X 射线然后 ZSTK474 的联合治疗,显著增强了细胞生长抑制作用。连续 ZSTK474 处理也观察到集落形成存活的联合效应。Western blot 分析显示 X 射线照射可增强 Akt 和 GSK-3β 的磷酸化,而 ZSTK474 单独处理则抑制磷酸化。X 射线照射后用 ZSTK474 处理也抑制了磷酸化,并显著抑制了异种移植肿瘤的生长。X 射线和 ZSTK474 的联合治疗在体外和体内均具有比单独放疗或药物治疗更大的治疗潜力。