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首页> 外文期刊>Turkish journal of biology >A letter in response to 'Cancer stem cells: emerging actors in both basic and clinical cancer research' Turk J Biol (2014) 38: (c) TUBITAK - doi:10.3906/biy-1406-93 Cancer stem cells (CSCs): targets and strategies for intervention
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A letter in response to 'Cancer stem cells: emerging actors in both basic and clinical cancer research' Turk J Biol (2014) 38: (c) TUBITAK - doi:10.3906/biy-1406-93 Cancer stem cells (CSCs): targets and strategies for intervention

机译:回应“癌症干细胞:基础和临床癌症研究中的新兴角色”的一封信。Turk J Biol(2014)38:(c)TUBITAK-doi:10.3906 / biy-1406-93癌症干细胞(CSC):目标和干预策略

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摘要

This letter to the editor highlights the important aspects of cancer stem cells and provides a deeper insight into the origin and characterization of these cells as well as the mechanisms contributing to drug resistance and relapse. The two currently available models (CSC and the clonal evolution model) need not be mutually exclusive to explain the origin of CSCs. The identification of CSCs (based on surface markers, drug efflux, enzyme activity, and signal transduction molecules and proteins involved in EMT processes) can help in discriminating these cells from other cell types. Moreover, CSCs prefer a hypoxic environment. This microenvironmental cue can trigger certain metabolic alterations that can orchestrate a rewiring of the epigenome. Consequently, changes in transcription factors and signaling molecules can contribute to the plasticity/inter-convertibility of the CSCs and non-CSC cellular states. Hence, an improved understanding of the mechanisms involved also provides opportunities for pharmacological manipulations. This letter also underscores the presence of precancerous stem cells as well as very small embryonic-like stem cells (VSELs) (both considered to be precursors of CSCs). These reports warrant a thorough reanalysis of the source of CSCs (lineage tracing studies), subsequent to the development of better targeted intervention approaches.
机译:给编辑的这封信强调了癌症干细胞的重要方面,并提供了对这些细胞的起源和特征以及导致耐药性和复发的机制的更深入的了解。当前两个可用的模型(CSC和克隆进化模型)不需要相互排斥即可解释CSC的起源。 CSC的识别(基于表面标记,药物外流,酶活性以及与EMT过程有关的信号转导分子和蛋白质)可以帮助将这些细胞与其他细胞类型区分开。此外,CSC更喜欢低氧环境。这种微环境提示可以触发某些新陈代谢的改变,从而可以安排表观基因组的重新布线。因此,转录因子和信号分子的变化可有助于CSC和非CSC细胞状态的可塑性/相互转化性。因此,对所涉及机制的更好理解也为药理操作提供了机会。这封信还强调了癌前干细胞以及非常小的胚胎样干细胞(VSEL)(均被视为CSC的前体)的存在。这些报告需要在开发出更好的针对性干预方法之后,对CSC的来源(血统追踪研究)进行彻底的重新分析。

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