Department of Electrical Engineering, The Pennsylvania State University, University Park, PA, 16801, USA.
Department of Biomedical Engineering, The Pennsylvania State University, University Park, PA, USA.
Sci Rep. 2024 Oct 9;14(1):23560. doi: 10.1038/s41598-024-73688-y.
Collective cancer invasion exhibits a hierarchical structure characterized by leader-follower organization. Dynamic gene expression analysis of invading cells using nanobiosensors within 3D microenvironments provides a valuable means to explore the regulation of leader cells during collective cancer invasion. Nonetheless, the analysis of time-lapse, multimodal images that capture the intricacies of complex invading structures and gene expression profiles in 3D tumor spheroids poses a significant technological challenge. Here, we present a computer vision-based workflow that streamlines the identification of protrusions and detached clusters from 3D tumor spheroids. This methodology not only discerns invading multicellular structures and quantifies their physical properties, but also captures gene expression patterns associated with these invasive mechanisms using an intracellular nanobiosensor. Consequently, it empowers a systematic exploration of the genotypic and phenotypic heterogeneities inherent in cancer invasion. To illustrate the effectiveness of this approach, we applied it to the analysis of a long noncoding RNA, MALAT1, in tumor spheroids derived from patients with muscle-invasive bladder cancer. Our investigation delved into the heterogeneity of cancer invasion and its relationship to MALAT1 expression. Overall, this workflow represents a valuable tool for gaining insights into the complexities of cancer invasion.
肿瘤的集体浸润表现出一种层级结构,其特征是领导者-追随者的组织形式。利用纳米生物传感器在 3D 微环境中对浸润细胞进行动态基因表达分析,为探索集体肿瘤浸润过程中领导者细胞的调控提供了有价值的手段。然而,对捕获复杂浸润结构和 3D 肿瘤球体中基因表达谱的时间推移、多模态图像的分析仍然是一个重大的技术挑战。在这里,我们提出了一种基于计算机视觉的工作流程,用于简化从 3D 肿瘤球体中识别突起和分离簇。这种方法不仅可以区分浸润性的多细胞结构并量化它们的物理特性,还可以使用细胞内纳米生物传感器捕获与这些浸润机制相关的基因表达模式。因此,它能够系统地探索癌症浸润中固有的遗传和表型异质性。为了说明这种方法的有效性,我们将其应用于分析源自肌肉浸润性膀胱癌患者的肿瘤球体中的长非编码 RNA MALAT1。我们的研究深入探讨了癌症浸润的异质性及其与 MALAT1 表达的关系。总的来说,该工作流程代表了一种深入了解癌症浸润复杂性的有价值的工具。