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细胞竞争驱动上皮肿瘤形成果蝇模型中转移性肿瘤的形成。

Cell Competition Drives the Formation of Metastatic Tumors in a Drosophila Model of Epithelial Tumor Formation.

作者信息

Eichenlaub Teresa, Cohen Stephen M, Herranz Héctor

机构信息

Department of Cellular and Molecular Medicine, University of Copenhagen, Blegdamsvej 3, Copenhagen 2200 N, Denmark.

Department of Cellular and Molecular Medicine, University of Copenhagen, Blegdamsvej 3, Copenhagen 2200 N, Denmark; Institute of Molecular and Cell Biology, 61 Biopolis Drive, Singapore 138673, Singapore.

出版信息

Curr Biol. 2016 Feb 22;26(4):419-27. doi: 10.1016/j.cub.2015.12.042. Epub 2016 Feb 4.

Abstract

Cell competition is a homeostatic process in which proliferating cells compete for survival. Elimination of otherwise normal healthy cells through competition is important during development and has recently been shown to contribute to maintaining tissue health during organismal aging. The mechanisms that allow for ongoing cell competition during adult life could, in principle, contribute to tumorigenesis. However, direct evidence supporting this hypothesis has been lacking. Here, we provide evidence that cell competition drives tumor formation in a Drosophila model of epithelial cancer. Cells expressing EGFR together with the conserved microRNA miR-8 acquire the properties of supercompetitors. Neoplastic transformation and metastasis depend on the ability of these cells to induce apoptosis and engulf nearby cells. miR-8 expression causes genome instability by downregulating expression of the Septin family protein Peanut. Cytokinesis failure due to downregulation of Peanut is required for tumorigenesis. This study provides evidence that the cellular mechanisms that drive cell competition during normal tissue growth can be co-opted to drive tumor formation and metastasis. Analogous mechanisms for cytokinesis failure may lead to polyploid intermediates in tumorigenesis in mammalian cancer models.

摘要

细胞竞争是一种稳态过程,在此过程中增殖细胞为生存而竞争。在发育过程中,通过竞争消除原本正常健康的细胞很重要,并且最近已表明这有助于在机体衰老过程中维持组织健康。原则上,成年期持续进行细胞竞争的机制可能有助于肿瘤发生。然而,一直缺乏支持这一假说的直接证据。在此,我们提供证据表明,在果蝇上皮癌模型中细胞竞争驱动肿瘤形成。与保守的微小RNA miR-8一起表达表皮生长因子受体(EGFR)的细胞获得了超级竞争者的特性。肿瘤转化和转移取决于这些细胞诱导凋亡并吞噬附近细胞的能力。miR-8表达通过下调Septin家族蛋白花生(Peanut)的表达导致基因组不稳定。花生表达下调导致的胞质分裂失败是肿瘤发生所必需的。这项研究提供证据表明,在正常组织生长过程中驱动细胞竞争的细胞机制可被用于驱动肿瘤形成和转移。胞质分裂失败的类似机制可能导致哺乳动物癌症模型肿瘤发生过程中出现多倍体中间体。

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