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治疗浓度的抗癫痫药物不能抑制溶瘤腺病毒 Delta24-RGD 在恶性神经胶质瘤中的活性。

Therapeutic concentrations of anti-epileptic drugs do not inhibit the activity of the oncolytic adenovirus Delta24-RGD in malignant glioma.

机构信息

Department of Neurosurgery, Erasmus MC, Rotterdam, The Netherlands.

出版信息

J Gene Med. 2013 Mar-Apr;15(3-4):134-41. doi: 10.1002/jgm.2703.

Abstract

BACKGROUND

The oncolytic adenovirus Delta24-RGD is currently being tested in phase I trials for the treatment of glioblastoma (GBM). Literature suggests that frequently prescribed anticonvulsants for these patients, phenytoin (PHE), valproic acid (VPA) and levetiracetam (LEV), may interfere with cellular mechanisms of cancer or oncolytic virus activity. We therefore investigated the direct effects of these drugs on Delta24-RGD infection and oncolytic activity.

METHODS

The anticonvulsants PHE, VPA, and LEV were combined with Delta24-RGD treatment in established glioma cell lines as well as on a panel of patient-derived GBM cultures. Effects on infection efficiency were assessed using luciferase-encoding adenoviral vectors. Oncolytic activity was determined by WST-1 assay and viral progeny production was quantified by dilution titration.

RESULTS

IC50 values of the anti-epileptic drugs on the four glioma cell lines were far above clinically-relevant concentrations. At therapeutic concentrations, the anti-epileptics generally did not alter the infection efficiency of RGD-modified adenovirus, nor affect progeny production or oncolytic activity of Delta24-RGD. The only exception was found in U373 cells, where VPA slightly antagonised the oncolytic effect of Delta24-RGD (from 29% to 55% viability, p<0.01) as well as viral progeny production (60% decrease, p<0.01). Oncolysis by Delta24-RGD was not inhibited by the anti-epileptics in any of the patient-derived glioma cultures (n=6). In fact, in one culture a slight enhancement of viral oncolysis by PHE and LEV was found, from 89.7% viability to 76% and 62.4%, respectively (p<0.01)

CONCLUSIONS

Therapeutic levels of valproic acid, phenytoin and levetiracetam do not negatively interfere with the infection efficiency or oncolytic activity of Delta24-RGD in patient-derived GBM cells. Therefore, there is no indication that the choice of anticonvulsant for seizure control in glioma patients should take treatment with Delta24-RGD into account.

摘要

背景

溶瘤腺病毒 Delta24-RGD 目前正在进行治疗胶质母细胞瘤(GBM)的 I 期临床试验。文献表明,这些患者经常开的抗癫痫药苯妥英(PHE)、丙戊酸(VPA)和左乙拉西坦(LEV)可能会干扰癌症的细胞机制或溶瘤病毒的活性。因此,我们研究了这些药物对 Delta24-RGD 感染和溶瘤活性的直接影响。

方法

将抗癫痫药 PHE、VPA 和 LEV 与 Delta24-RGD 联合用于已建立的神经胶质瘤细胞系以及一系列患者来源的 GBM 培养物中。使用编码荧光素酶的腺病毒载体评估感染效率。通过 WST-1 测定法确定溶瘤活性,并通过稀释滴定法定量测定病毒产物的产生。

结果

四种神经胶质瘤细胞系的抗癫痫药物的 IC50 值远高于临床相关浓度。在治疗浓度下,抗癫痫药通常不会改变 RGD 修饰的腺病毒的感染效率,也不会影响 Delta24-RGD 的病毒产物产生或溶瘤活性。唯一的例外是在 U373 细胞中,VPA 略微拮抗了 Delta24-RGD 的溶瘤作用(从 29%降至 55%的活力,p<0.01)以及病毒产物的产生(减少 60%,p<0.01)。在任何患者来源的神经胶质瘤培养物中(n=6),Delta24-RGD 的溶瘤作用均未被抗癫痫药抑制。事实上,在一种培养物中,发现 PHE 和 LEV 略微增强了病毒的溶瘤作用,从 89.7%的活力分别降至 76%和 62.4%(p<0.01)。

结论

治疗水平的丙戊酸、苯妥英和左乙拉西坦不会对 Delta24-RGD 在患者来源的 GBM 细胞中的感染效率或溶瘤活性产生负面影响。因此,没有迹象表明,在胶质母细胞瘤患者中选择抗癫痫药来控制癫痫发作时,应考虑使用 Delta24-RGD。

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