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利用特定遗传因子将原代人星形胶质细胞快速重编程为强效肿瘤起始细胞

Rapid Reprogramming of Primary Human Astrocytes into Potent Tumor-Initiating Cells with Defined Genetic Factors.

作者信息

Li Fang, Liu Xinjian, Sampson John H, Bigner Darell D, Li Chuan-Yuan

机构信息

Department of Dermatology, Duke University Medical Center, Durham, North Carolina.

Department of Neurosurgery, Duke University Medical Center, Durham, North Carolina. Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, North Carolina.

出版信息

Cancer Res. 2016 Sep 1;76(17):5143-50. doi: 10.1158/0008-5472.CAN-16-0171. Epub 2016 Jun 30.

Abstract

Cancer stem-like cells (CSC) are thought to drive brain cancer, but their cellular and molecular origins remain uncertain. Here, we report the successful generation of induced CSC (iCSC) from primary human astrocytes through the expression of defined genetic factors. Combined transduction of four factors, Myc, Oct-4, p53DD, and Ras, induced efficient transformation of primary human astrocytes into malignant cells with powerful tumor-initiating capabilities. Notably, transplantation of 100 transduced cells into nude mice was sufficient for tumor formation. The cells showed unlimited self-renewal ability with robust telomerase activities. In addition, they expressed typical glioma stem-like cell markers, such as CD133, CD15, and CD90. Moreover, these cells could form spheres in culture and differentiate into neuron-like, astrocyte-like, and oligodendrocyte-like cells. Finally, they also displayed resistance to the widely used brain cancer drug temozolomide. These iCSCs could provide important tools for studies of glioma biology and therapeutics development. Cancer Res; 76(17); 5143-50. ©2016 AACR.

摘要

癌症干细胞(CSC)被认为是引发脑癌的原因,但其细胞和分子起源仍不明确。在此,我们报告了通过表达特定基因因子成功从原代人星形胶质细胞诱导生成诱导性癌症干细胞(iCSC)。Myc、Oct-4、p53DD和Ras这四种因子的联合转导可有效将原代人星形胶质细胞转化为具有强大肿瘤起始能力的恶性细胞。值得注意的是,将100个转导细胞移植到裸鼠体内就足以形成肿瘤。这些细胞表现出无限的自我更新能力,端粒酶活性强劲。此外,它们表达典型的胶质瘤干细胞样细胞标志物,如CD133、CD15和CD90。而且,这些细胞在培养中可形成球体,并分化为神经元样、星形胶质细胞样和少突胶质细胞样细胞。最后,它们还对广泛使用的脑癌药物替莫唑胺表现出抗性。这些诱导性癌症干细胞可为胶质瘤生物学研究和治疗方法开发提供重要工具。《癌症研究》;76(17);5143 - 50。©2016美国癌症研究协会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33dd/5082736/bd8c1e45978e/nihms800335f1.jpg

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