U-981, Gustave Roussy, Villejuif, France.
Department of Translational Research, Institut Curie, Paris, France.
Nat Cell Biol. 2018 Mar;20(3):296-306. doi: 10.1038/s41556-017-0027-6. Epub 2018 Feb 5.
Metastases account for 90% of cancer-related deaths; thus, it is vital to understand the biology of tumour dissemination. Here, we collected and monitored >50 patient specimens ex vivo to investigate the cell biology of colorectal cancer (CRC) metastatic spread to the peritoneum. This reveals an unpredicted mode of dissemination. Large clusters of cancer epithelial cells displaying a robust outward apical pole, which we termed tumour spheres with inverted polarity (TSIPs), were observed throughout the process of dissemination. TSIPs form and propagate through the collective apical budding of hypermethylated CRCs downstream of canonical and non-canonical transforming growth factor-β signalling. TSIPs maintain their apical-out topology and use actomyosin contractility to collectively invade three-dimensional extracellular matrices. TSIPs invade paired patient peritoneum explants, initiate metastases in mice xenograft models and correlate with adverse patient prognosis. Thus, despite their epithelial architecture and inverted topology TSIPs seem to drive the metastatic spread of hypermethylated CRCs.
转移占癌症相关死亡的 90%;因此,了解肿瘤扩散的生物学特性至关重要。在这里,我们收集并监测了 >50 个患者标本的离体情况,以研究结直肠癌(CRC)转移到腹膜的细胞生物学。这揭示了一种出乎意料的扩散模式。在整个扩散过程中,我们观察到大量显示出强大外向顶端的癌细胞簇,我们将其称为具有倒置极性的肿瘤球体(TSIPs)。TSIPs 通过经典和非经典转化生长因子-β信号下游的高甲基化 CRC 的集体顶端出芽形成和传播。TSIPs 保持其顶端向外的拓扑结构,并利用肌动球蛋白收缩性进行集体入侵三维细胞外基质。TSIPs 侵袭配对的患者腹膜外植体,在小鼠异种移植模型中引发转移,并与患者不良预后相关。因此,尽管具有上皮结构和倒置拓扑结构,TSIPs 似乎可以驱动高甲基化 CRC 的转移扩散。