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本文引用的文献

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Targeting self-renewal, an Achilles' heel of cancer stem cells.靶向自我更新,这是癌症干细胞的致命弱点。
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Growth differentiating factor 15 enhances the tumor-initiating and self-renewal potential of multiple myeloma cells.生长分化因子 15 增强多发性骨髓瘤细胞的肿瘤起始和自我更新能力。
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Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma.突变分析揭示了复发性神经胶质瘤的起源和治疗驱动的进化。
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Cell fate factor DACH1 represses YB-1-mediated oncogenic transcription and translation.细胞命运因子 DACH1 抑制 YB-1 介导的致癌转录和翻译。
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Self-renewal as a therapeutic target in human colorectal cancer.人类结直肠癌治疗靶点的自我更新。
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6
Prostate cancer originating in basal cells progresses to adenocarcinoma propagated by luminal-like cells.前列腺癌起源于基底细胞,然后进展为腔细胞样细胞增殖的腺癌。
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Vitamin C modulates TET1 function during somatic cell reprogramming.维生素 C 在体细胞重编程过程中调节 TET1 功能。
Nat Genet. 2013 Dec;45(12):1504-9. doi: 10.1038/ng.2807. Epub 2013 Oct 27.
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Does the microenvironment influence the cell types of origin for prostate cancer?微环境是否影响前列腺癌的细胞起源类型?
Genes Dev. 2013 Jul 15;27(14):1539-44. doi: 10.1101/gad.222380.113.
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Distinct FAK activities determine progenitor and mammary stem cell characteristics.不同的 FAK 活性决定祖细胞和乳腺干细胞的特征。
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Generation of cancer stem-like cells through the formation of polyploid giant cancer cells.通过多倍体巨癌细胞的形成产生癌症干细胞样细胞。
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癌症干细胞:不断进化且功能异质的治疗靶点。

Cancer stem cells: constantly evolving and functionally heterogeneous therapeutic targets.

机构信息

Authors' Affiliations: Research Center for Translational Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China; and Department of Molecular Carcinogenesis, the University of Texas MD Anderson Cancer Center, Science Park, Smithville, Texas

Authors' Affiliations: Research Center for Translational Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China; and Department of Molecular Carcinogenesis, the University of Texas MD Anderson Cancer Center, Science Park, Smithville, Texas.

出版信息

Cancer Res. 2014 Jun 1;74(11):2922-7. doi: 10.1158/0008-5472.CAN-14-0266. Epub 2014 Apr 8.

DOI:10.1158/0008-5472.CAN-14-0266
PMID:24713433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4112560/
Abstract

Elucidating the origin of and dynamic interrelationship between intratumoral cell subpopulations has clear clinical significance in helping to understand the cellular basis of treatment response, therapeutic resistance, and tumor relapse. Cancer stem cells (CSC), together with clonal evolution driven by genetic alterations, generate cancer cell heterogeneity commonly observed in clinical samples. The 2013 Shanghai International Symposium on Cancer Stem Cells brought together leaders in the field to highlight the most recent progress in phenotyping, characterizing, and targeting CSCs and in elucidating the relationship between the cell-of-origin of cancer and CSCs. Discussions from the symposium emphasize the urgent need in developing novel therapeutics to target the constantly evolving CSCs.

摘要

阐明肿瘤内细胞亚群的起源和动态相互关系,对于帮助理解治疗反应、治疗耐药性和肿瘤复发的细胞基础具有明确的临床意义。癌症干细胞 (CSC) 与遗传改变驱动的克隆进化一起,产生了临床上常见的肿瘤细胞异质性。2013 年上海癌症干细胞国际研讨会汇集了该领域的领导者,重点介绍了在表型分析、特征描述和靶向 CSC 方面的最新进展,并阐明了癌症起源细胞与 CSC 之间的关系。会议讨论强调了迫切需要开发针对不断进化的 CSC 的新型治疗方法。