Scemama Alice, Lunetto Sophia, Tailor Artysha, Di Cio Stefania, Dibble Matthew, Gautrot Julien, Biddle Adrian
Blizard Institute, Queen Mary University of London, London, E1 2AT, UK.
Queen Mary University of London, London, England, UK.
F1000Res. 2024 Jan 15;12:439. doi: 10.12688/f1000research.131810.2. eCollection 2023.
Metastasis occurs when cancer cells leave the primary tumour and travel to a secondary site to form a new lesion. The tumour microenvironment (TME) is recognised to greatly influence this process, with for instance the vascular system enabling the dissemination of the cells into other tissues. However, understanding the exact role of these microenvironmental cells during metastasis has proven challenging. Indeed, models often appear too simplistic, and the study of the interactions between different cell types in a 3D space is limited. On the other hand, even though models incorporate the TME, observing cells in real-time to understand their exact role is difficult. Horizontal compartmentalised microfluidic models are a promising new platform for metastasis studies. These devices, composed of adjacent microchannels, can incorporate multiple cell types within a 3D space. Furthermore, the transparency and thickness of these models also enables high quality real-time imaging to be performed. This paper demonstrates how these devices can be successfully used for oral squamous cell carcinoma (OSCC) metastasis studies, focusing on the role of the vascular system in this process. Conditions for co-culture of OSCC cells and endothelial cells have been determined and staining protocols optimised. Furthermore, several imaging analysis techniques for these models are described, enabling precise segmentation of the different cell types on the images as well as accurate assessment of their phenotype. These methods can be applied to any study aiming to understand the role of microenvironmental cell types in cancer metastatic dissemination, and overcome several challenges encountered with current and models. Hence, this new model capable of recapitulating important aspects of the cellular complexity of human metastatic dissemination can ultimately contribute to replacing animal studies in this field.
当癌细胞离开原发肿瘤并转移至继发部位形成新的病灶时,就会发生转移。肿瘤微环境(TME)被认为对这一过程有很大影响,例如血管系统能使癌细胞扩散到其他组织中。然而,要了解这些微环境细胞在转移过程中的确切作用已被证明具有挑战性。实际上,相关模型往往显得过于简单,而且在三维空间中研究不同细胞类型之间相互作用的研究有限。另一方面,尽管模型纳入了肿瘤微环境,但实时观察细胞以了解其确切作用却很困难。水平分区微流控模型是转移研究中一个很有前景的新平台。这些由相邻微通道组成的装置,可以在三维空间中纳入多种细胞类型。此外,这些模型的透明度和厚度也使得高质量的实时成像得以进行。本文展示了这些装置如何成功用于口腔鳞状细胞癌(OSCC)转移研究,重点关注血管系统在这一过程中的作用。已经确定了OSCC细胞与内皮细胞共培养的条件,并优化了染色方案。此外,还描述了针对这些模型的几种成像分析技术,能够在图像上精确分割不同的细胞类型,并准确评估它们的表型。这些方法可应用于任何旨在了解微环境细胞类型在癌症转移扩散中作用的研究,并克服了当前模型所面临的若干挑战。因此,这种能够概括人类转移扩散细胞复杂性重要方面的新模型最终有助于取代该领域的动物研究。