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本文引用的文献

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The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.2016 年世界卫生组织中枢神经系统肿瘤分类:概述。
Acta Neuropathol. 2016 Jun;131(6):803-20. doi: 10.1007/s00401-016-1545-1. Epub 2016 May 9.
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A combined gene signature of hypoxia and notch pathway in human glioblastoma and its prognostic relevance.人类胶质母细胞瘤中缺氧与Notch信号通路的联合基因特征及其预后相关性
PLoS One. 2015 Mar 3;10(3):e0118201. doi: 10.1371/journal.pone.0118201. eCollection 2015.
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Growth arrest and forced differentiation of human primary glioblastoma multiforme by a novel small molecule.一种新型小分子诱导人原发性多形性胶质母细胞瘤生长停滞并促进其分化
Sci Rep. 2014 Jul 3;4:5546. doi: 10.1038/srep05546.
4
Sox2 promotes malignancy in glioblastoma by regulating plasticity and astrocytic differentiation.Sox2通过调节可塑性和星形胶质细胞分化促进胶质母细胞瘤的恶性发展。
Neoplasia. 2014 Mar;16(3):193-206, 206.e19-25. doi: 10.1016/j.neo.2014.03.006. Epub 2014 Apr 13.
5
Sox2 is required to maintain cancer stem cells in a mouse model of high-grade oligodendroglioma.Sox2 在高级少突胶质细胞瘤的小鼠模型中维持癌症干细胞。
Cancer Res. 2014 Mar 15;74(6):1833-44. doi: 10.1158/0008-5472.CAN-13-1942. Epub 2014 Mar 5.
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Correlation between the prognostic value and the expression of the stem cell marker CD133 and isocitrate dehydrogenase1 in glioblastomas.胶质母细胞瘤中干细胞标志物 CD133 和异柠檬酸脱氢酶 1 的表达与预后价值的相关性。
J Neurooncol. 2013 Dec;115(3):333-41. doi: 10.1007/s11060-013-1234-z. Epub 2013 Oct 16.
7
Serum-free culture success of glial tumors is related to specific molecular profiles and expression of extracellular matrix-associated gene modules.无血清培养胶质肿瘤的成功与特定的分子谱和细胞外基质相关基因模块的表达有关。
Neuro Oncol. 2013 Dec;15(12):1684-95. doi: 10.1093/neuonc/not116. Epub 2013 Sep 17.
8
Concise review: the involvement of SOX2 in direct reprogramming of induced neural stem/precursor cells.简明综述:SOX2 在诱导性神经干细胞/前体细胞的直接重编程中的作用。
Stem Cells Transl Med. 2013 Aug;2(8):579-83. doi: 10.5966/sctm.2012-0179. Epub 2013 Jul 1.
9
Astrocytoma grade IV (glioblastoma multiforme) displays 3 subtypes with unique expression profiles of intermediate filament proteins.星形细胞瘤 4 级(多形性胶质母细胞瘤)表现出 3 种亚型,具有独特的中间丝蛋白表达谱。
Hum Pathol. 2013 Oct;44(10):2081-8. doi: 10.1016/j.humpath.2013.03.013. Epub 2013 Jun 18.
10
Specific expression pattern of a novel Otx2 splicing variant during neural differentiation.新型 Otx2 剪接变异体在神经分化过程中的特异性表达模式。
Gene. 2013 Jul 1;523(1):33-8. doi: 10.1016/j.gene.2013.03.114. Epub 2013 Apr 5.

通过贴壁培养对CD133/SOX2胶质母细胞瘤干细胞进行选择性富集。

Selective enrichment of CD133/SOX2 glioblastoma stem cells via adherent culture.

作者信息

Lv Ke, Chen Zhenyu, Zhang Xiaoqing, Zhang Quanbin, Liu Ling

机构信息

Neurosurgical Department, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200092, P.R. China.

Neuroregeneration Key Laboratory of Shanghai Universities, Tongji University School of Medicine, Shanghai 200092, P.R. China.

出版信息

Oncol Lett. 2018 Oct;16(4):4567-4576. doi: 10.3892/ol.2018.9154. Epub 2018 Jul 17.

DOI:10.3892/ol.2018.9154
PMID:30197675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6126346/
Abstract

Most of the brain tumors are malignant with an extremely poor survival rate. Recent progress in identifying cancer stem cells (CSCs) within the brain tumors is starting to revolutionize our understanding in the imitation and progression of tumors as well as relapse and the development of therapeutic strategies. Suspension spheroid body culture paradigm is a routine method in enriching CSCs. While, it was reported recently that CSCs within the brain tumor may also be enriched through adherent monolayer culture with optimized properties. In the present study, 18 surgically resected brain tumors were used for analyzing the feasibility of adherent enrichment of CSCs. The results indicated that 50% of glioblastomas were able to generate adherent CSCs, which were uniformly positive for Sox2, CD133, GFAP and Nestin. However, adherent culture paradigm failed to yield CSCs in secondary brain tumors, including neurocytomas, ependymomas, germ cell tumors or low-grade astrocytomas, which is most likely due to a lack of CD133/Sox2 cells within the original biopsies. Therefore, it was concluded that the adherent culture paradigm may serve as a reliable method in enriching brain CSCs, but this method is more suitable for enriching CD133/Sox2 CSCs in glioblastomas.

摘要

大多数脑肿瘤是恶性的,生存率极低。最近在脑肿瘤中识别癌症干细胞(CSCs)方面取得的进展,正开始彻底改变我们对肿瘤的发生、发展以及复发和治疗策略制定的理解。悬浮球体培养模式是富集CSCs的常规方法。然而,最近有报道称,脑肿瘤中的CSCs也可以通过具有优化特性的贴壁单层培养来富集。在本研究中,使用18例手术切除的脑肿瘤来分析贴壁富集CSCs的可行性。结果表明,50%的胶质母细胞瘤能够产生贴壁CSCs,这些细胞对Sox2、CD133、GFAP和巢蛋白均呈阳性。然而,贴壁培养模式未能在继发性脑肿瘤中产生CSCs,包括神经细胞瘤、室管膜瘤、生殖细胞瘤或低级别星形细胞瘤,这很可能是由于原始活检组织中缺乏CD133/Sox2细胞。因此,得出的结论是,贴壁培养模式可能是富集脑CSCs的可靠方法,但这种方法更适合于富集胶质母细胞瘤中的CD133/Sox2 CSCs。