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Neural Stem Cell-based Gene Therapy for Brain Tumors

机译:基于神经干细胞的脑肿瘤基因治疗

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Advances in gene-based medicine since 1990s have ushered in new therapeutic strategy of gene therapy for inborn error genetic diseases and cancer. Malignant brain tumors such as glioblastoma multiforme and medulloblastoma remain virtually untreatable and lethal. Currently available treatment for brain tumors including radical surgical resection followed by radiation and chemotherapy, have substantially improved the survival rate in patients suffering from these brain tumors; however, it remains incurable in large proportion of patients. Therefore, there is substantial need for effective, low-toxicity therapies for patients with malignant brain tumors, and gene therapy targeting brain tumors should fulfill this requirement. Gene therapy for brain tumors includes many therapeutic strategies and these strategies can be grouped in two major categories: molecular and immunologic. The widely used molecular gene therapy approach is suicide gene therapy based on the conversion of non-toxic prodrugs into active anticancer agents via introduction of enzymes and genetic immunotherapy involves the gene transfer of immune-stimulating cytokines including IL-4, IL-12 and TRAIL. For both molecular and immune gene therapy, neural stem cells (NSCs) can be used as delivery vehicle of therapeutic genes. NSCs possess an inherent tumor tropism that supports their use as a reliable delivery vehicle to target therapeutic gene products to primary brain tumors and metastatic cancers throughout the brain. Significance of the NSC-based gene therapy for brain tumor is that it is possible to exploit the tumor-tropic property of NSCs to mediate effective, tumor-selective therapy for primary and metastatic cancers in the brain and outside, for which no tolerated curative treatments are currently available.
机译:自1990年代以来,基于基因的医学取得了新进展,迎来了针对先天性遗传病和癌症的基因治疗新治疗策略。恶性脑瘤,例如多形性胶质母细胞瘤和髓母细胞瘤,实际上仍然无法治愈且具有致命性。目前可用的脑肿瘤治疗方法包括根治性手术切除,然后放疗和化疗,已大大改善了患有这些脑肿瘤的患者的生存率;但是,它仍然无法治愈大部分患者。因此,非常需要针对恶性脑肿瘤患者的有效的低毒性疗法,并且针对脑肿瘤的基因疗法应满足该要求。脑肿瘤的基因治疗包括许多治疗策略,这些策略可分为两大类:分子和免疫学。广泛使用的分子基因疗法是自杀基因疗法,其基础是通过引入酶将无毒前药转化为活性抗癌药,而遗传免疫疗法则涉及免疫刺激细胞因子(包括IL-4,IL-12和TRAIL)的基因转移。对于分子和免疫基因治疗,神经干细胞(NSC)都可以用作治疗基因的传递载体。 NSC具有固有的肿瘤嗜性,支持将其用作可靠的载体,将治疗性基因产物靶向整个脑部的原发性脑肿瘤和转移性癌症。基于NSC的基因疗法对脑肿瘤的意义在于,可以利用NSC的向肿瘤特性来介导针对脑内外的原发性和转移性癌症的有效,肿瘤选择性治疗,对此没有耐受的治疗方法目前可用。

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