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肿瘤干细胞中端粒酶下调

Telomerase downregulation in cancer brain stem cell.

机构信息

Brain Tumour North West, Faculty of Science and Technology, University of Central Lancashire, Preston, UK.

出版信息

Mol Cell Biochem. 2009 Nov;331(1-2):153-9. doi: 10.1007/s11010-009-0153-y. Epub 2009 May 9.

Abstract

Cancer stem cells (CSCs) are a minute sub-population of self-renewing, immortal cells, which can be responsible for chemoresistance observed in the treatment of cancer. CSCs are similar to cancer cells requiring telomerase activity or alternative mechanisms for their proliferation and regeneration. This study explored the correlation between CD133 (stem cell marker) and telomerase expression using CD133+ cells isolated from the glioma GOS-3 cell line with magnetic affinity cell sorting (MACS). GOS-3 CD133+ showed a transcription downregulation of hTERT ( approximately 100-fold decrease) compared with CD133- cells. In order to further substantiate the novel finding, serum deprivation was adopted to enrich CD133 expression in GOS-3 cells. A pronounced upregulation of cd133 and downregulation of telomerase expression were produced as a consequence of decreasing serum supplement levels in GOS-3 cells. These findings showed for the first time that telomerase is downregulated in brain cancer stem cells compared to cancer cells.

摘要

癌症干细胞(CSC)是一小部分自我更新、永生的细胞,它们可能是导致癌症治疗中观察到的化疗耐药的原因。CSC 类似于需要端粒酶活性或其他机制来增殖和再生的癌细胞。本研究使用从神经胶质瘤 GOS-3 细胞系中分离的 CD133+细胞通过磁性亲和细胞分选(MACS),探讨了 CD133(干细胞标志物)与端粒酶表达之间的相关性。与 CD133-细胞相比,GOS-3 CD133+细胞的 hTERT 转录下调(约 100 倍)。为了进一步证实这一新发现,采用血清剥夺法在 GOS-3 细胞中富集 CD133 表达。随着 GOS-3 细胞中血清补充水平的降低,cd133 的表达明显上调,端粒酶的表达下调。这些发现首次表明,与癌细胞相比,脑癌干细胞中端粒酶下调。

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