Cheung Kevin J, Ewald Andrew J
Department of Cell Biology, Center for Cell Dynamics, School of Medicine, Johns Hopkins University, 855 N. Wolfe St, 452 Rangos Bldg, Baltimore, MD 21205, USA; Department of Oncology, School of Medicine, Johns Hopkins University, 855 N. Wolfe St, 452 Rangos Bldg, Baltimore, MD 21205, USA.
Curr Opin Cell Biol. 2014 Oct;30:99-111. doi: 10.1016/j.ceb.2014.07.003. Epub 2014 Aug 17.
Metastasis begins when tumors invade into surrounding tissues. In breast cancer, the study of cell interactions has provided fundamental insights into this complex process. Powerful intravital and 3D organoid culture systems have emerged that enable biologists to model the complexity of cell interactions during cancer invasion in real-time. Recent studies utilizing these techniques reveal distinct mechanisms through which multiple cancer cell and stromal cell subpopulations interact, including paracrine signaling, direct cell-cell adhesion, and remodeling of the extracellular matrix. Three cell interaction mechanisms have emerged to explain how breast tumors become invasive: epithelial-mesenchymal transition, collective invasion, and the macrophage-tumor cell feedback loop. Future work is needed to distinguish whether these mechanisms are mutually exclusive or whether they cooperate to drive metastasis.
转移始于肿瘤侵入周围组织。在乳腺癌中,对细胞相互作用的研究为这一复杂过程提供了基本见解。强大的活体和三维类器官培养系统已经出现,使生物学家能够实时模拟癌症侵袭过程中细胞相互作用的复杂性。最近利用这些技术进行的研究揭示了多种癌细胞和基质细胞亚群相互作用的不同机制,包括旁分泌信号传导、直接细胞间粘附以及细胞外基质的重塑。已经出现了三种细胞相互作用机制来解释乳腺肿瘤如何变得具有侵袭性:上皮-间质转化、集体侵袭和巨噬细胞-肿瘤细胞反馈回路。需要未来的研究来区分这些机制是相互排斥的,还是它们协同作用以驱动转移。