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Immune response to bacteria induces dissemination of Ras-activated Drosophila hindgut cells

机译:对细菌的免疫反应诱导Ras激活的果蝇后肠细胞的传播

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摘要

Although pathogenic bacteria are suspected contributors to colorectal cancer progression, cancer-promoting bacteria and their mode of action remain largely unknown. Here we report that sustained infection with the human intestinal colonizer Pseudomonas aeruginosa synergizes with the Ras1V12 oncogene to induce basal invasion and dissemination of hindgut cells to distant sites. Cross-talk between infection and dissemination requires sustained activation by the bacteria of the Imd–dTab2–dTak1 innate immune pathway, which converges with Ras1V12 signalling on JNK pathway activation, culminating in extracellular matrix degradation. Hindgut, but not midgut, cells are amenable to this cooperative dissemination, which is progressive and genetically and pharmacologically inhibitable. Thus, Drosophila hindgut provides a valuable system for the study of intestinal malignancies.
机译:尽管怀疑致病菌是导致结直肠癌进展的因素,但促癌细菌及其作用方式仍是未知之数。在这里,我们报道人类肠道菌落铜绿假单胞菌的持续感染与Ras1 V12 癌基因协同作用,诱导基础侵袭和后肠细胞向远处的扩散。感染和传播之间的串扰需要Imd–dTab2–dTak1先天性免疫途径的细菌持续激活,该途径与JNK途径激活的Ras1 V12 信号融合,最终导致细胞外基质降解。后肠细胞而不是中肠细胞适合这种合作性传播,这种合作性传播是渐进的并且在遗传和药理学上是可抑制的。因此,果蝇后肠为肠道恶性肿瘤的研究提供了有价值的系统。

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