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果蝇中 JNK 介导的吞噬作用消除致癌性邻居。

Elimination of oncogenic neighbors by JNK-mediated engulfment in Drosophila.

机构信息

Department of Cell Biology, G-COE, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.

出版信息

Dev Cell. 2011 Mar 15;20(3):315-28. doi: 10.1016/j.devcel.2011.02.007.

Abstract

A newly emerged oncogenic cell in the epithelial population has to confront antitumor selective pressures in the host tissue. However, the mechanisms by which surrounding normal tissue exerts antitumor effects against oncogenically transformed cells are poorly understood. In Drosophila imaginal epithelia, clones of cells mutant for evolutionarily conserved tumor suppressor genes such as scrib or dlg lose their epithelial integrity and are eliminated from epithelia when surrounded by wild-type tissue. Here, we show that surrounding normal cells activate nonapoptotic JNK signaling in response to the emergence of oncogenic mutant cells. This JNK activation leads to upregulation of PVR, the Drosophila PDGF/VEGF receptor. Genetic and time-lapse imaging analyses reveal that PVR expression in surrounding cells activates the ELMO/Mbc-mediated phagocytic pathway, thereby eliminating oncogenic neighbors by engulfment. Our data indicate that JNK-mediated cell engulfment could be an evolutionarily conserved intrinsic tumor-suppression mechanism that eliminates premalignant cells from epithelia.

摘要

上皮群体中新生的致癌细胞必须在宿主组织中面对抗肿瘤的选择性压力。然而,周围正常组织对致癌转化细胞发挥抗肿瘤作用的机制还知之甚少。在果蝇的 imaginal 上皮中,细胞克隆突变体对于进化上保守的肿瘤抑制基因如 scrib 或 dlg 的上皮完整性丧失,并且当被野生型组织包围时从上皮中消除。在这里,我们表明周围正常细胞在响应致癌突变细胞的出现时激活非凋亡性 JNK 信号。这种 JNK 激活导致果蝇 PDGF/VEGF 受体 PVR 的上调。遗传和延时成像分析表明,周围细胞中 PVR 的表达激活了 ELMO/Mbc 介导的吞噬途径,从而通过吞噬作用消除致癌的邻近细胞。我们的数据表明,JNK 介导的细胞吞噬作用可能是一种进化上保守的内在肿瘤抑制机制,可将前恶性细胞从上皮中消除。

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