Bauman G S, Fisher B J, McDonald W, Amberger V R, Moore E, Del Maestro R F
Department of Radiation Oncology, London Regional Cancer Clinic, University of Western Ontario, Canada.
Int J Dev Neurosci. 1999 Aug-Oct;17(5-6):643-51. doi: 10.1016/s0736-5748(99)00023-4.
An experimental model of malignant glioma growth involving implantation of spheroids into a gel matrix of collagen type I has been developed. This model has been used to characterize changes in glioma cell invasion in response to single dose and fractionated radiation treatment. Suspensions of C6 astrocytoma cells were grown in spinner culture flasks to yield spheroids of varying size (300-1000 microm). Implantation of spheroids into a gel matrix of collagen type I was associated with measurable invasion of the surrounding gel by individual tumor cells. Changes in the distance of invasion in response to single dose and fractionated radiation were measured. Changes in apoptosis and proliferative indices in different regions of the spheroids in response to radiation were also assessed. In unirradiated gels, maximum depth of invasion, 1300-1750 microm, was achieved by 5 days after implantation. A radiation dose-dependent inhibition of invasion was noted and was most profound for larger spheroids. Fractionation of the radiation dose was associated with a partial recovery of invasion. Changes in apoptotic and proliferative indices in response to radiation depended on the region of the spheroid examined. Increases in apoptosis were noted for cells at the surface of the spheroid and invading cells while cells at the centre of the spheroid demonstrated virtually no increase in apoptosis. Likewise, a dose-dependent decrease in proliferative indices following radiation was noted among the invading cells and cells at the surface of the spheroid but not at the centre of the spheroid. We have described a model of malignant glioma invasion which possesses many of the qualities of in vivo malignant gliomas. Within this model, invasion appeared to be inhibited by radiation in a dose- and fractionation-dependent fashion. Measurement of apoptotic and cell proliferation indices favour a direct cytotoxic effect on the invading cells as the most likely mechanism for this phenomenon.
已建立了一种恶性胶质瘤生长的实验模型,该模型涉及将球体植入I型胶原凝胶基质中。此模型已用于表征胶质瘤细胞在单次剂量和分次放射治疗后的侵袭变化。将C6星形细胞瘤细胞悬液在旋转培养瓶中培养以产生不同大小(300 - 1000微米)的球体。将球体植入I型胶原凝胶基质中会导致单个肿瘤细胞对周围凝胶的可测量侵袭。测量了单次剂量和分次放射后侵袭距离的变化。还评估了球体不同区域对放射的凋亡和增殖指数变化。在未照射的凝胶中,植入后5天达到最大侵袭深度,为1300 - 1750微米。观察到放射剂量依赖性的侵袭抑制,对较大球体最为显著。放射剂量的分次与侵袭的部分恢复相关。放射后凋亡和增殖指数的变化取决于所检查的球体区域。球体表面和侵袭细胞的凋亡增加,而球体中心的细胞凋亡几乎没有增加。同样,放射后侵袭细胞和球体表面细胞的增殖指数呈剂量依赖性下降,但球体中心细胞未出现这种情况。我们描述了一种恶性胶质瘤侵袭模型,该模型具有许多体内恶性胶质瘤的特征。在这个模型中,侵袭似乎受到放射的剂量和分次依赖性抑制。凋亡和细胞增殖指数的测量表明,对侵袭细胞的直接细胞毒性作用是这种现象最可能的机制。