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干细胞在脑肿瘤替代治疗中的应用:基因递送的潜力

Stem cell in alternative treatments for brain tumors: potential for gene delivery.

作者信息

Mariotti Veronica, Greco Steven J, Mohan Ryan D, Nahas George R, Rameshwar Pranela

机构信息

Department of Medicine - Hematology/Oncology, New Jersey Medical School, Rutgers School of Biomedical Sciences, E-585, 185 South Orange Avenue, Newark, NJ 07103 USA.

Stowers Institute for Medical Research, Kansas City, MO USA.

出版信息

Mol Cell Ther. 2014 Aug 1;2:24. doi: 10.1186/2052-8426-2-24. eCollection 2014.

DOI:10.1186/2052-8426-2-24
PMID:26056591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4451968/
Abstract

Despite ongoing research efforts and attempts to bring new drugs into trial, the prognosis for brain tumors remains poor. Patients with the most common and lethal intracranial neoplasia, glioblastoma multiforme (GBM), have an average survival of one year with combination of surgical resection, radiotherapy and temozolomide. One of the main problems in the treatment of GBM is getting drugs across the blood brain barrier (BBB) efficiently. In an attempt to solve this problem, there are ongoing experimental and clinical trials to deliver drugs within stem cells. The purpose for this method is the ease by which stem cells home to the brain. This review discusses the experimental and clinical applications of stem cells for GBM. We also discuss the different properties of stem cells. This information is important to understand why one stem cell would be advantageous over another in cell therapy. We provide an overview of the different drug delivery methods, gene-based treatments and cancer vaccines for GBM, including the stem cell subset.

摘要

尽管一直在进行研究并努力将新药带入临床试验,但脑肿瘤的预后仍然很差。患有最常见且致命的颅内肿瘤——多形性胶质母细胞瘤(GBM)的患者,通过手术切除、放疗和替莫唑胺联合治疗,平均生存期为一年。治疗GBM的主要问题之一是如何有效地使药物穿过血脑屏障(BBB)。为了解决这个问题,目前正在进行将药物递送至干细胞内的实验和临床试验。这种方法的目的是利用干细胞归巢至脑部的便利性。本综述讨论了干细胞在GBM中的实验和临床应用。我们还讨论了干细胞的不同特性。了解这些信息对于理解在细胞治疗中一种干细胞为何比另一种更具优势很重要。我们概述了针对GBM的不同药物递送方法基于基因的治疗和癌症疫苗,包括干细胞亚群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e66/4451968/7da710a75d7c/40591_2014_28_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e66/4451968/5767ca77b3c4/40591_2014_28_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e66/4451968/7da710a75d7c/40591_2014_28_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e66/4451968/5767ca77b3c4/40591_2014_28_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e66/4451968/7da710a75d7c/40591_2014_28_Fig2_HTML.jpg

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本文引用的文献

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EGFRvIII-specific chimeric antigen receptor T cells migrate to and kill tumor deposits infiltrating the brain parenchyma in an invasive xenograft model of glioblastoma.在胶质母细胞瘤的侵袭性异种移植模型中,表皮生长因子受体III型变异体(EGFRvIII)特异性嵌合抗原受体T细胞迁移至浸润脑实质的肿瘤沉积物并将其杀死。
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Neuropsychiatric Lupus, the Blood Brain Barrier, and the TWEAK/Fn14 Pathway.神经精神性狼疮、血脑屏障与TWEAK/Fn14信号通路
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