腺病毒基因治疗高度恶性胶质瘤。

Rebecca Pedersini, Emanuela Vattemi, Pier Paolo Claudio
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引用次数: 6

摘要

尽管手术技术的进步,放射治疗和化疗的改进,以及新的生物制剂的加入,近几十年来,高度恶性胶质瘤患者的中位生存期几乎没有变化。然而,对脑肿瘤生物学的基本认识的进展表明,靶向致癌的分子途径可能为胶质瘤治疗提供替代或额外的方法。病毒,特别是腺病毒,在这些分子方法的应用和发展中起着关键作用。腺病毒已被设计为基因治疗的载体,用于传递治疗基因,并作为溶瘤病毒治疗的直接细胞毒剂。本文综述的目的是展望腺病毒在高度恶性胶质瘤治疗中的应用。
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Adenoviral gene therapy in high-grade malignant glioma.

Despite advances in surgical techniques, improvement in radiation treatments and chemotherapy, and the addition of new biological agents to the armamentarium, the median survival of patients with high-grade malignant glioma has changed little over recent decades. However, advances in the fundamental understanding of brain tumor biology suggest that targeting molecular pathways underlying carcinogenesis may provide alternative or additional approaches to glioma treatment. Viruses, particularly adenoviruses, have been critical in the application and development of these molecular approaches. Adenoviruses have been engineered to function as vectors for delivering therapeutic genes for gene therapy, and as direct cytotoxic agents for oncolytic viral therapy. The purpose of this review is to provide a prospective on the use of adenoviruses in high-grade malignant glioma therapy.

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来源期刊
Drug news & perspectives
Drug news & perspectives 医学-药学
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