Milker-Zabel Stefanie, Zabel-du Bois Angelika, Ranai Gholamreza, Trinh Thuy, Unterberg Andreas, Debus Jürgen, Lipson Kenneth E, Abdollahi Amir, Huber Peter E
Department of Radiation Oncology, University of Heidelberg, Heidelberg, Germany.
Int J Radiat Oncol Biol Phys. 2008 Mar 15;70(4):1213-8. doi: 10.1016/j.ijrobp.2007.11.041. Epub 2008 Jan 30.
To analyze the effect of the multireceptor tyrosine kinase inhibitor SU11657 (primarily vascular endothelial growth factor, platelet-derived growth factor) in combination with irradiation in freshly isolated primary human meningioma cells.
Tumor specimens were obtained from meningioma patients undergoing surgery at the Department of Neurosurgery, University of Heidelberg, Germany. For the present study only cells up to passage 6 were used. Benign and atypical meningioma cells and human umbilical vein endothelial cells (HUVEC) were treated with SU11657 alone and in combination with 6-MV photons (0-10 Gy). Clonogenic survival and cell proliferation were determined alone and in coculture assays to determine direct and paracrine effects.
Radiation and SU11657 alone reduced cell proliferation in atypical and benign meningioma cells as well as in HUVEC in a dose-dependent manner. SU11657 alone also reduced clonogenic survival of benign and atypical meningioma cells. SU11657 increased radiosensitivity of human meningioma cells in clonogenic survival and cell number/proliferation assays. The anticlonogenic and antiproliferative effects alone and the radiosensitization effects of SU11657 were more pronounced in atypical meningioma cells compared with benign meningioma cells.
Small-molecule tyrosine kinase inhibitors like SU11657 are capable of amplifying the growth inhibitory effects of irradiation in meningioma cells. These data provide a rationale for further clinical evaluation of this combination concept, especially in atypical and malignant meningioma patients.
分析多受体酪氨酸激酶抑制剂SU11657(主要作用于血管内皮生长因子、血小板衍生生长因子)联合放疗对新鲜分离的原代人脑膜瘤细胞的影响。
肿瘤标本取自德国海德堡大学神经外科接受手术的脑膜瘤患者。本研究仅使用传代6次以内的细胞。分别单独用SU11657以及将其与6兆伏光子(0 - 10戈瑞)联合处理良性和非典型脑膜瘤细胞以及人脐静脉内皮细胞(HUVEC)。通过单独培养和共培养试验测定克隆形成存活率和细胞增殖情况,以确定直接和旁分泌效应。
单独放疗和SU11657均以剂量依赖方式降低非典型和良性脑膜瘤细胞以及HUVEC的细胞增殖。单独使用SU11657也降低了良性和非典型脑膜瘤细胞的克隆形成存活率。在克隆形成存活率和细胞数量/增殖试验中,SU11657提高了人脑膜瘤细胞的放射敏感性。与良性脑膜瘤细胞相比,SU11657单独的抗克隆形成和抗增殖作用以及放射增敏作用在非典型脑膜瘤细胞中更为明显。
像SU11657这样的小分子酪氨酸激酶抑制剂能够增强放疗对脑膜瘤细胞的生长抑制作用。这些数据为进一步临床评估这种联合方案提供了理论依据,尤其是在非典型和恶性脑膜瘤患者中。