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单染色体增益可作为结肠癌转移抑制因子和促进因子。

Single-Chromosomal Gains Can Function as Metastasis Suppressors and Promoters in Colon Cancer.

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA; Google, Inc., New York, NY 10011, USA.

出版信息

Dev Cell. 2020 Feb 24;52(4):413-428.e6. doi: 10.1016/j.devcel.2020.01.034.

Abstract

High levels of cancer aneuploidy are frequently associated with poor prognosis. To examine the relationship between aneuploidy and cancer progression, we analyzed a series of congenic cell lines that harbor single extra chromosomes. We found that across 13 different trisomic cell lines, 12 trisomies suppressed invasiveness or were largely neutral, while a single trisomy increased metastatic behavior by triggering a partial epithelial-mesenchymal transition. In contrast, we discovered that chromosomal instability activates cGAS/STING signaling but strongly suppresses invasiveness. By analyzing patient copy-number data, we demonstrate that specific aneuploidies are associated with distinct outcomes, and the acquisition of certain aneuploidies is in fact linked with a favorable prognosis. Thus, aneuploidy is not a uniform driver of malignancy, and different aneuploidies can uniquely influence tumor progression. At the same time, the gain of a single chromosome is capable of inducing a profound cell state transition, thereby linking genomic plasticity, phenotypic plasticity, and metastasis.

摘要

高水平的癌症非整倍体经常与预后不良相关。为了研究非整倍体与癌症进展之间的关系,我们分析了一系列携带单个额外染色体的同基因细胞系。我们发现,在 13 种不同的三体细胞系中,12 种三体抑制了侵袭性或基本呈中性,而单一的三体通过触发部分上皮-间充质转化增加了转移性行为。相比之下,我们发现染色体不稳定性激活了 cGAS/STING 信号,但强烈抑制了侵袭性。通过分析患者的拷贝数数据,我们证明了特定的非整倍体与不同的结果相关,并且某些非整倍体的获得实际上与预后良好相关。因此,非整倍体并不是恶性的统一驱动因素,不同的非整倍体可以独特地影响肿瘤的进展。同时,单个染色体的获得能够诱导细胞状态的深刻转变,从而将基因组可塑性、表型可塑性和转移联系起来。

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