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散发性嗜铬细胞瘤发生中肿瘤干细胞样细胞的意义。

Implication of tumor stem-like cells in the tumorigenesis of sporadic paraganglioma.

机构信息

Developmental & Stem Cell Institute, Department of Gynecology, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.

出版信息

Med Oncol. 2013 Dec;30(4):659. doi: 10.1007/s12032-013-0659-8. Epub 2013 Aug 31.

Abstract

It is commonly believed that paragangliomas are rare tumors arising from the neural crest-derived chromaffin cells. Although it has been speculated that paraganglioma is related to stem cell origin, there has been lack of direct evidence demonstrating the presence of (neural) stem cells in these tumor tissues. In this study, we found a subgroup of human paraganglioma from ten clinical samples displayed definitive markers of CD133 and/or nestin, the fundamental features of neural stem cell capable of self-renewal and differentiation. A panel of lineage-specific markers was also manifest in some of these tumors, consistent with the hierarchical and heterogeneous nature of these tumors. These observations strongly suggest that at least some forms of paraganglioma maintain tumor stem-like cells (TSCs) that potentially contribute to the histologic complexity of human paraganglioma. Finally, we found that the genomic DNA structure becomes highly unstable in tumor cells of paraganglioma, indicating the loss of tight control of genomic surveillance system be an important transitory event from normal multi-potent tissue stem cells to TSCs.

摘要

人们普遍认为,嗜铬细胞瘤是源自神经嵴来源的嗜铬细胞的罕见肿瘤。虽然有人推测嗜铬细胞瘤与干细胞起源有关,但缺乏直接证据表明这些肿瘤组织中存在(神经)干细胞。在这项研究中,我们从十个临床样本中发现了一部分人类嗜铬细胞瘤,这些肿瘤表现出 CD133 和/或巢蛋白的明确标记,这些标记是具有自我更新和分化能力的神经干细胞的基本特征。这些肿瘤中的一些还表现出一系列谱系特异性标记,符合这些肿瘤的层次和异质性性质。这些观察结果强烈表明,至少某些形式的嗜铬细胞瘤维持着肿瘤干细胞样细胞(TSC),这些细胞可能有助于人类嗜铬细胞瘤的组织学复杂性。最后,我们发现,嗜铬细胞瘤肿瘤细胞的基因组 DNA 结构变得高度不稳定,表明基因组监测系统的紧密控制丧失是从正常多能组织干细胞到 TSC 的一个重要过渡事件。

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