通过慢病毒感染,选择性消耗带有染色体外DNA的癌细胞。

IF 3.3 Q3 ONCOLOGY
Eunhee Yi, Amit D Gujar, Dacheng Zhao, Kentaro Suina, Xue Jin, Katharina Pardon, Qinghao Yu, Larisa Kagermazova, Emmanuel E Korsah, Noah A Dusseau, Jef D Boeke, Anton G Henssen, Roel G W Verhaak
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引用次数: 0

摘要

染色体外DNA (ecDNA)是在癌症中发现的一种主要的局灶性癌基因扩增模式,最近作为一种新兴的癌症标志重新受到关注,在癌症中普遍存在。随着技术的进步,如高覆盖测序和活细胞基因组成像,我们现在可以研究ecDNA的行为和功能。然而,我们仍然缺乏对如何消除ecDNA的理解。当我们试图研究ecDNA行为的机制时,我们观察到含有ecDNA的细胞在慢病毒而不是转座子转导过程中耗竭。这一发现可能为在新兴的ecDNA研究中利用慢病毒系统提供重要信息。此外,这一观察结果表明具有ecDNA的细胞具有特异性敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective Depletion of Cancer Cells with Extrachromosomal DNA via Lentiviral Infection.

Extrachromosomal DNA (ecDNA), a major focal oncogene amplification mode found across cancer, has recently regained attention as an emerging cancer hallmark, with a pervasive presence across cancers. With technical advancements such as high-coverage sequencing and live-cell genome imaging, we can now investigate the behaviors and functions of ecDNA. However, we still lack an understanding of how to eliminate ecDNA. We observed depletion of cells containing ecDNA during lentiviral but not transposon-based transduction, whereas we sought to investigate the mechanism of ecDNA behavior. This discovery may provide critical information on utilizing a lentiviral system in emerging ecDNA research. Additionally, this observation suggests specific sensitivities for cells with ecDNA.

Significance: ecDNA is an essential factor in cancer progression. We found that a group of cancer cells with ecDNA is selectively depleted after lentiviral infection. This finding provides promise for ecDNA-specific targeting, suggests the need for caution in using lentivirus, and offers alternative ways to study ecDNA.

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