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病毒载体作为胶质母细胞瘤的治疗药物。

Viral vectors as therapeutic agents for glioblastoma.

作者信息

Aghi Manish, Rabkin Samuel

机构信息

Massachusetts General Hospital and Harvard Medical School, Department of Neurosurgery, Molecular Neurosurgery Laboratory, Boston, MA 02114, USA.

出版信息

Curr Opin Mol Ther. 2005 Oct;7(5):419-30.

Abstract

Established treatments such as surgery, radiation and chemotherapy have not altered the median survival of glioblastoma, the most common malignant brain tumor. Since these failures reflect the highly invasive nature of glioblastoma, as well as the fact that few cells are actively replicating at any given point in time, therapies need to act in areas of the brain distant from the site of tumor origin and for long after their introduction. Over the past decade, laboratory studies and early clinical trials have raised hope that these therapeutic requirements may be fulfilled by gene therapy using non-replicating transgene-bearing viruses, oncolytic viruses or migratory stem cells to deliver tumoricidal transgenes. The principles behind these approaches and their initial results are reviewed.

摘要

诸如手术、放疗和化疗等既定治疗方法并未改变胶质母细胞瘤(最常见的恶性脑肿瘤)的中位生存期。由于这些治疗失败反映了胶质母细胞瘤的高度侵袭性,以及在任何给定时间点很少有细胞在积极复制这一事实,因此治疗需要在远离肿瘤起源部位的脑区发挥作用,并且在引入治疗后很长时间内持续发挥作用。在过去十年中,实验室研究和早期临床试验带来了希望,即使用携带非复制性转基因的病毒、溶瘤病毒或迁移干细胞进行基因治疗来递送杀肿瘤转基因,可能满足这些治疗需求。本文综述了这些方法背后的原理及其初步结果。

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