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基于干细胞的恶性脑胶质瘤治疗。

Stem cell-based therapy for malignant glioma.

机构信息

Lund Stem Cell Center, BMC B10, Lund University, Lund, Sweden; Molecular Medicine, Center for Molecular Pathology, Lund University, Skåne University Hospital, Malmö, Sweden.

出版信息

Cancer Treat Rev. 2013 Jun;39(4):358-65. doi: 10.1016/j.ctrv.2012.06.006. Epub 2012 Jul 13.

Abstract

Stem cells have been extensively investigated as tumour-tropic vectors for gene delivery to solid tumours. In this review, we discuss the potential for using stem cells as cellular vector systems in gene therapy for malignant gliomas, with a focus on neural stem cells, and multipotent mesenchymal stromal cells. Tumour cell-derived substances and factors associated with tumour-induced inflammation and tumour neovascularisation can specifically attract stem cells to invasive gliomas. Injected stem cells engineered to produce anti-tumour substances have shown strong therapeutic effects in experimental glioma models. However, the potential caveats include the immunosuppressive functions of multipotent mesenchymal stromal cells, the contribution of stem cells to the pro-tumourigenic stroma, and the malignant transformation of implanted stem cells. In addition, it is not yet known which stem cell types and therapeutic genes will be most effective for the treatment of glioma patients. Here, we highlight the possibilities and problems for translating promising experimental findings in glioma models into the clinic.

摘要

干细胞作为肿瘤趋向性载体,已被广泛研究用于将基因递送至实体瘤。在这篇综述中,我们讨论了使用干细胞作为恶性神经胶质瘤基因治疗中细胞载体系统的潜力,重点是神经干细胞和多能间充质基质细胞。肿瘤细胞衍生的物质和与肿瘤诱导的炎症及肿瘤新生血管生成相关的因子,可以特异性地吸引干细胞浸润侵袭性神经胶质瘤。经基因工程改造以产生抗肿瘤物质的注入干细胞,在实验性神经胶质瘤模型中显示出很强的治疗效果。然而,潜在的问题包括多能间充质基质细胞的免疫抑制功能、干细胞对促肿瘤性基质的贡献,以及植入干细胞的恶性转化。此外,尚不清楚哪种干细胞类型和治疗基因对治疗神经胶质瘤患者最有效。在这里,我们强调了将有前途的实验结果转化为神经胶质瘤模型临床应用的可能性和问题。

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