Gene Delivery in Neuro-Oncology

被引:22
作者
Dixit, Karan [1 ]
Kumthekar, Priya [1 ]
机构
[1] Northwestern Univ, Div Neurooncol, Dept Neurol, 710 N Lake Shore Dr,Abbott Hall Room 1123, Chicago, IL 60611 USA
关键词
Gene therapy; Stemcells; Nanoparticles; Viral vectors; Glioblastoma; High-grade glioma; HERPES-SIMPLEX-VIRUS; NEURAL STEM-CELLS; THYMIDINE KINASE GENE; HIGH-GRADE GLIOMA; PHASE-I TRIAL; RECURRENT GLIOBLASTOMA-MULTIFORME; RETROVIRAL REPLICATING VECTOR; HUMAN-MALIGNANT GLIOMA; INTRAVENOUS GANCICLOVIR; THERAPEUTIC-EFFICACY;
D O I
10.1007/s11912-017-0628-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review Glioblastoma multiforme (GBM) is the most common primary malignant brain tumor in adults with a dismal prognosis despite aggressive multimodal management thus novel treatments are urgently needed. Gene therapy is a versatile treatment strategy being investigated in multiple cancers including GBM. In gene therapy, a variety of vectors or "carriers" are used to deliver genes designed for different anti-tumoral effects. Gene delivery vehicles and approaches to treatment will be addressed in this review. Recent Findings The most commonly studied vectors are viral based, however, driven by advances in biomedical engineering, mesenchymal and neural stem cells, as well as multiple different types of nanoparticles have been developed to improve tumor tropism and also increase gene transfer into tumor cells. Different genes have been studied including suicide genes, which convert non-toxic prodrug into cytotoxic drug; immunomodulatory genes, which stimulate the immune system; and tumor suppressor genes which repair the defect that allow cells to divide unchecked. Summary Gene therapy may be a promising treatment strategy in neuro-oncology as it is versatile and flexible due to the ability to tailor vectors and genes for specific therapeutic activity. Pre-clinical studies and clinical trials have demonstrated feasibility and safety of gene therapy; however, further studies are required to determine efficacy.
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页数:11
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