An investigation of the viscoelastic properties and the actin cytoskeletal structure of triple negative breast cancer cells. (October 2018)

• Record Type: Journal Article
• Authors: Hu, Jingjie; Zhou, Yuxiao; Obayemi, John D.; Du, Jing; Soboyejo, Winston O.
• Is Part Of: Journal of the mechanical behavior of biomedical materials. Volume 86(2018)
• Page Start: 1
• Page End: 13
• Publication Date: 2018-10
• Subjects: Shear assay method -- Digital image correlation -- Cell viscoelasticity -- Actin cytoskeletal structure -- Cancer diagnosis; Biomedical materials -- Periodicals; Biomedical materials -- Mechanical properties -- Periodicals; Biomedical materials; Biomedical materials -- Mechanical properties; Periodicals; Electronic journals; 610.28
• DOI: 10.1016/j.jmbbm.2018.05.038
• Languages: English
• ISSNs: 1751-6161

Abstract

Abstract: An improved understanding of the evolution of cell structure and viscoelasticity with cancer malignancy could enable the development of a new generation of biomarkers and methods for cancer diagnosis. Hence, in this study, we present the viscoelastic properties (moduli and viscosities) and the actin cytoskeletal structures of triple negative breast cancer (TNBC) cells with different metastatic potential. These include: MCF-10A normal breast cells (studied as a control); MDA-MB-468 cells (less metastatic TNBC cells), and MDA-MB-231 cells (highly metastatic TNBC cells). A combination of shear assay and digital imaging correlation (DIC) techniques is used to measure the local viscoelastic properties of live breast cells subjected to constant shear stress. The local moduli and viscosities of the nuclei and cytoplasm are characterized using a generalized Maxwell model, which is used to determine the time-dependent creep responses of cells. The nuclei are shown to be stiffer and more viscous than the cytoplasms of the normal breast cells and TNBC cells. The MCF-10A normal breast cells are found to be twice as stiff as the less metastatic MDA-MB-468 breast cancer cells and over ten times stiffer than the highly metastatic MDA-MB-231 breast cancer cells. Similar trends are also observed in the viscosities of the nuclei and the cytoplasms. The measured differences in cell viscoelastic properties are also associated with significant changes in the cell cytoskeletal structure, which is studied using confocal fluorescence microscopy. This reveals significant differences in the levels of actin expression and organization in TNBC cells as they become highly metastatic. Our results suggest that the shear assay measurements of cell viscoelastic properties may be used as effective biomarkers for TNBC diagnosis and screening. Graphical abstract: fx1 Highlights: Combined shear assay and DIC method can measure local cell viscoelasticity. TNBC cells can be differentiated from normal breast cells based on viscoelasticity. TNBC cell viscoelasticity correlates with their actin cytoskeletal structure. Shear assay and DIC approaches provides new insights for TNBC screening.