Université Lille, Inserm, CHU Lille, U1192, Laboratoire Protéomique, Réponse Inflammatoire Et Spectrométrie de Masse (PRISM), Equipe Labellisée Ligue Contre le Cancer, Lille, France.
University Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, US 41 - UAR 2014 - PLBS, F-59000 Lille, France.
Cell Rep Methods. 2024 Jun 17;4(6):100792. doi: 10.1016/j.crmeth.2024.100792. Epub 2024 Jun 10.
3D tumoroids have revolutionized in vitro/ex vivo cancer biology by recapitulating the complex diversity of tumors. While tumoroids provide new insights into cancer development and treatment response, several limitations remain. As the tumor microenvironment, especially the immune system, strongly influences tumor development, the absence of immune cells in tumoroids may lead to inappropriate conclusions. Macrophages, key players in tumor progression, are particularly challenging to integrate into the tumoroids. In this study, we established three optimized and standardized methods for co-culturing human macrophages with breast cancer tumoroids: a semi-liquid model and two matrix-embedded models tailored for specific applications. We then tracked interactions and macrophage infiltration in these systems using flow cytometry and light sheet microscopy and showed that macrophages influenced not only tumoroid molecular profiles but also chemotherapy response. This underscores the importance of increasing the complexity of 3D models to more accurately reflect in vivo conditions.
3D 类器官通过重现肿瘤的复杂多样性,彻底改变了体外/体内癌症生物学。虽然类器官为癌症发展和治疗反应提供了新的见解,但仍存在一些局限性。由于肿瘤微环境(特别是免疫系统)强烈影响肿瘤的发展,类器官中缺乏免疫细胞可能导致不恰当的结论。巨噬细胞是肿瘤进展的关键参与者,特别难以整合到类器官中。在这项研究中,我们建立了三种优化和标准化的方法,用于将人源巨噬细胞与乳腺癌类器官共培养:一种半液体模型和两种针对特定应用的基质嵌入模型。然后,我们使用流式细胞术和光片显微镜跟踪这些系统中的相互作用和巨噬细胞浸润,并表明巨噬细胞不仅影响类器官的分子特征,还影响化疗反应。这突显了增加 3D 模型复杂性以更准确地反映体内条件的重要性。