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DNA-Demethylating Agents Target Colorectal Cancer Cells by Inducing Viral Mimicry by Endogenous Transcripts

机译:通过内源性转录物诱导病毒模拟,DNA-去甲基化剂靶聚结肠癌细胞

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摘要

DNA-demethylating agents have shown clinical antitumor efficacy via an unknown mechanism of action. Using a combination of experimental and bioinformatics analyses in colorectal cancer cells, we demonstrate that low-dose 5-AZA-CdR targets colorectal cancer-initiating cells (CICs) by inducing viral mimicry. This is associated with induction of dsRNAs derived at least in part from endogenous retroviral elements, activation of the MDA5/MAVS RNA recognition pathway, and downstream activation of IRF7. Indeed, disruption of virus recognition pathways, by individually knocking down MDA5, MAVS, or IRF7, inhibits the ability of 5-AZA-CdR to target colorectal CICs and significantly decreases 5-AZA-CdR long-term growth effects. Moreover, transfection of dsRNA into CICs can mimic the effects of 5-AZA-CdR. Together, our results represent a major shift in understanding the anti-tumor mechanisms of DNA-demethylating agents and highlight the MDA5/MAVS/IRF7 pathway as a potentially druggable target against CICs.
机译:DNA-去甲基化试剂通过未知的作用机制显示临床抗肿瘤功效。使用实验性和生物信息学分析的结肠直肠癌细胞的组合,我们证明了低剂量5-AZA-CDR通过诱导病毒模拟物来靶心结直肠癌引发细胞(CICS)。这与至少部分地来自内源性逆转录病毒元素的DSRNA诱导相关,MDA5 / MAVS RNA识别途径的激活以及IRF7的下游活化。实际上,通过单独敲降MDA5,MAVS或IRF7来抑制5-AZA-CDR至靶结肠直肠CICS的能力并显着降低5-AZA-CDR长期生长效应的干扰。此外,将DSRNA转染到CICS可以模拟5-AZA-CDR的影响。我们的结果在一起代表了了解DNA - 去甲基化试剂的抗肿瘤机制并突出MDA5 / MAVS / IRF7途径作为对CICS的潜在可用的目标的重大转变。

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  • 来源
    《Cell》 |2015年第5期|共13页
  • 作者单位

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Univ So Calif Keck Sch Med Dept Urol Los Angeles CA 90089 USA;

    Univ So Calif Keck Sch Med Dept Urol Los Angeles CA 90089 USA;

    Univ So Calif Keck Sch Med Dept Urol Los Angeles CA 90089 USA;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

    Princess Margaret Canc Ctr Univ Hlth Network Toronto ON M5G 2M9 Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
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