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腺病毒基因疗法治疗高级别恶性胶质瘤

Adenoviral gene therapy in high-grade malignant glioma.

作者信息

Pedersini Rebecca, Vattemi Emanuela, Claudio Pier Paolo

机构信息

Division of Medical Oncology, Central Hospital, Bolzano, Italy.

出版信息

Drug News Perspect. 2010 Jul-Aug;23(6):368-79. doi: 10.1358/dnp.2010.23.6.1524009.

Abstract

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.

摘要

尽管手术技术有所进步,放射治疗和化疗有所改进,并且在治疗手段中增加了新的生物制剂,但近几十年来,高级别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取得的进展表明,针对致癌作用的分子途径进行靶向治疗可能为胶质瘤治疗提供替代方法或补充方法。病毒,尤其是腺病毒,在这些分子方法的应用和发展中发挥了关键作用。腺病毒已被改造为用于基因治疗的治疗性基因递送载体,以及用于溶瘤病毒治疗的直接细胞毒性剂。本综述的目的是对腺病毒在高级别恶性胶质瘤治疗中的应用进行展望。

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