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内质网应激诱导的分化使结肠癌干细胞对化疗敏感。

ER-Stress-Induced Differentiation Sensitizes Colon Cancer Stem Cells to Chemotherapy.

机构信息

Tytgat Institute for Liver and Intestinal Research and Department of Gastroenterology and Hepatology, Academic Medical Center, 1105 AZ Amsterdam, the Netherlands.

Laboratory of Experimental Oncology and Radiobiology, Academic Medical Center, 1105 AZ Amsterdam, the Netherlands.

出版信息

Cell Rep. 2015 Oct 20;13(3):489-494. doi: 10.1016/j.celrep.2015.09.016. Epub 2015 Oct 8.


DOI:10.1016/j.celrep.2015.09.016
PMID:26456824
Abstract

Colon cancer stem cells (colon-CSCs) are more resistant to conventional chemotherapy than differentiated cancer cells. This subset of therapy refractory cells is therefore believed to play an important role in post-therapeutic tumor relapse. In order to improve the rate of sustained response to conventional chemotherapy, development of approaches is warranted that specifically sensitize colon-CSCs to treatment. Here, we report that ER-stress-induced activation of the unfolded protein response (UPR) forces colon-CSCs to differentiate, resulting in their enhanced sensitivity to chemotherapy in vitro and in vivo. Our data suggest that agents that induce activation of the UPR may be used to specifically increase sensitivity of colon-CSCs to the effects of conventional chemotherapy.

摘要

结直肠肿瘤干细胞(colon-CSCs)比分化的肿瘤细胞对常规化疗更具有抗性。因此,人们认为这群对治疗有抗性的细胞在治疗后肿瘤复发中起重要作用。为了提高对常规化疗持续反应的比率,有必要开发专门使结肠肿瘤干细胞对治疗敏感的方法。在这里,我们报告 ER 应激诱导的未折叠蛋白反应(UPR)的激活迫使结肠肿瘤干细胞分化,导致它们在体外和体内对化疗的敏感性增强。我们的数据表明,诱导 UPR 激活的药物可用于特异性提高结肠肿瘤干细胞对常规化疗作用的敏感性。

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[7]
Long noncoding RNA 01534 maintains cancer stemness by downregulating endoplasmic reticulum stress response in colorectal cancer.

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