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CRAdRGDflt-IL24 virotherapy in combination with chemotherapy of experimental glioma

机译:CRAdRGDflt-IL24病毒疗法联合实验性神经胶质瘤化疗

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Malignant forms of glioma, the most common primary brain tumors, remain poorly responsive to multimodality therapeutic interventions, including chemotherapy. Suppressed apoptosis and extraordinary invasiveness are important distinctive features that contribute to the malignant phenotype of glioma. We have developed the vascular endothelial growth factor receptor 1 (VEGFR-1/flt-1) conditional replicating adenoviral vector (CRAdRGDflt-IL24) encoding the interleukin-24 (IL-24) gene. We investigated whether a combination of CRAdRGDflt-IL24-mediated oncolytic virotherapy and chemotherapy using temozolomide (TMZ) produces increased cytotoxicity against human glioma cells in comparison with these agents alone. Combination of CRAdRGDflt-IL24 and TMZ significantly enhanced cytotoxicity in vitro, inhibited D54MG tumor growth and prolonged survival of mice harboring intracranial human glioma xenografts in comparison with CRAdRGDflt-IL24 or TMZ alone. These data indicate that combined treatment with CRAdRGDflt-IL24-mediated oncolytic virotherapy and TMZ chemotherapy provides a promising approach for glioma therapy.
机译:恶性形式的神经胶质瘤(最常见的原发性脑部肿瘤)对包括化疗在内的多种治疗干预措施的反应仍然较差。抑制的细胞凋亡和非凡的侵袭性是导致神经胶质瘤恶性表型的重要特征。我们已经开发了编码白介素24(IL-24)基因的血管内皮生长因子受体1(VEGFR-1 / flt-1)条件复制腺病毒载体(CRAdRGDflt-IL24)。我们研究了与单独使用这些药物相比,使用替莫唑胺(TMZ)的CRAdRGDflt-IL24介导的溶瘤病毒疗法和化学疗法的组合是否产生针对人神经胶质瘤细胞的增加的细胞毒性。与单独使用CRAdRGDflt-IL24或TMZ相比,CRAdRGDflt-IL24和TMZ的组合在体外显着增强了细胞毒性,抑制了D54MG肿瘤的生长,并延长了携带颅内人神经胶质瘤异种移植物的小鼠的存活时间。这些数据表明,CRAdRGDflt-IL24介导的溶瘤病毒疗法和TMZ化疗的联合治疗为神经胶质瘤治疗提供了一种有希望的方法。

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