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作 者:张先稳[1] 刘永彪[2] 周强[3] 郝兴芝[3] 陈杰[3]
机构地区:[1]苏北人民医院放疗中心,江苏扬州225001 [2]徐州医学院肿瘤研究所,江苏徐州221002 [3]徐州医学院医学影像系,江苏徐州221002
出 处:《肿瘤防治杂志》2005年第20期1530-1534,共5页China Journal of Cancer Prevention and Treatment
基 金:国家自然科学基金(30200069)
摘 要:目的:探讨C60-AEDP对H22肝癌细胞和S180肉瘤细胞的影响及作用机制。方法:体外培养H22肝癌细胞和S180肉瘤细胞,MTT法观察药物在不同浓度、不同条件和不同时间下,对细胞生长方式的影响,FCM法了解其作用机制。结果:光照12h,C60-AEDP对H22和S180肿瘤细胞有生长抑制效应,呈浓度效应关系;在非光照条件下,C60-AEDP对H22和S180肿瘤细胞有生长抑制效应,呈浓度-时间效应关系;通过FCM观察,在光照条件下,C60-AEDP可引起G1/S周期阻滞;在非光照条件下,C60-AEDP可引起M/G1周期细胞阻滞;并都可引起细胞凋亡增加,H22、S180肿瘤细胞凋亡率在光照条件下分别增加了32%、26%,而非光照条件下分别增加了9%、5%。结论:在体外条件下,C60-AEDP在光照条件下和非光照条件下,均表现出对肿瘤细胞生长微弱的抑制效应。这种微弱的抑制效应可能是通过对细胞周期的影响而发挥作用。肿瘤防治杂志,2005,12(20)OBJECTIVE: To nvestigate the impact and mechanism of C60-AEDP to liver cancer cell H22 and sarcoma cell S180. METHODS: H22 and S180 cells were incubated at 96-hole board to observe effects of the drug on cell growth by MTT method, and to investigate the mechanism by FCM method. RESULTS: Under the illu mination condition for 12 h or not, it was demonstrated that C60-AEDP inhibited the growth of H22 and S180 cells, and the inhibitory rate was concentration- and time-dependents. C60 AEDP caused G1/S cycle block under illumination condition and M/G1 cycle block without illumination. The apoptosis rates of H22 and S180 cells were enhanced in the level of 32%, 260/00 under illumination condition, and 9%, 5% without illumination respectively. CONCLUSIONS: C60-AEDP has the slightly inhibitory effect on tumour cells of H22 and S180. It may be worked by the influence on cell cycle.
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