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鼻咽癌中 CD133(+)细胞的生物学特性。

Biological characteristics of CD133(+) cells in nasopharyngeal carcinoma.

机构信息

Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510080, P.R. China.

出版信息

Oncol Rep. 2013 Jul;30(1):57-63. doi: 10.3892/or.2013.2408. Epub 2013 Apr 22.

Abstract

Cancer stem cells are regarded as the cause of tumour formation and recurrence in nasopharyngeal carcinoma (NPC). However, ideal surface markers for stem cells in NPC remain unidentified. In the present study, we investigated the expression of CD133, Nanog and Sox2 in the nasopharyngeal carcinoma cell line CNE2 and primarily cultured NPC cells using immunofluorescence or flow cytometry. A cell population with a CD133(+) phenotype was enriched using magnetic-activated cell sorting technology. We demonstrated that CD133(+) cells exhibited a strong potential for self-renewal, proliferation and differentiation and a greater potential for in vivo tumour formation in nude mice compared to CD133(-) cells, although the percentage of CD133(+) cells was small. However, the specific marker antigens Nanog and Sox2 were simultaneously expressed in normal cancer stem cells. Our results showed that CD133 can serve as a specific surface marker for nasopharyngeal cancer stem cells.

摘要

癌症干细胞被认为是鼻咽癌(NPC)肿瘤形成和复发的原因。然而,NPC 中用于干细胞的理想表面标志物仍未被识别。在本研究中,我们使用免疫荧光或流式细胞术检测了 NPC 细胞系 CNE2 和原代培养的 NPC 细胞中 CD133、Nanog 和 Sox2 的表达。使用磁激活细胞分选技术富集具有 CD133(+)表型的细胞群。我们证明,与 CD133(-)细胞相比,CD133(+)细胞具有更强的自我更新、增殖和分化能力,并且在裸鼠体内形成肿瘤的能力更强,尽管 CD133(+)细胞的比例很小。然而,正常的癌症干细胞中同时表达了特异性标记抗原 Nanog 和 Sox2。我们的结果表明,CD133 可以作为鼻咽癌细胞干细胞的特异性表面标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee82/3729244/88bfa730034d/OR-30-01-0057-g00.jpg

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