Mechanical Properties and Nanomotion of BT-20 and ZR-75 Breast Cancer Cells Studied by Atomic Force Microscopy and Optical Nanomotion Detection Method

Author:

Starodubtseva Maria N.12ORCID,Shkliarava Nastassia M.2ORCID,Chelnokova Irina A.2ORCID,Villalba María I.34,Krylov Andrei Yu.5,Nadyrov Eldar A.6ORCID,Kasas Sandor34

Affiliation:

1. Department of Medical and Biological Physics, Gomel State Medical University, 246000 Gomel, Belarus

2. Laboratory of the Stability of Biological Systems, Radiobiology Institute of NAS of Belarus, 246007 Gomel, Belarus

3. Laboratory of Biological Electron Microscopy, Ecole Polytechnique Fédérale de Lausanne (EPFL), University of Lausanne (UNIL), 1015 Lausanne, Switzerland

4. Centre Universitaire Romand de Médecine Légale, UFAM, University of Lausanne, 1015 Lausanne, Switzerland

5. Department of Forensic Medicine, Institute of Further Training and Retraining of the Personnel, State Forensic Examination Committee of the Republic of Belarus, 220033 Minsk, Belarus

6. Department of Histology, Cytology and Embryology, Gomel State Medical University, 246000 Gomel, Belarus

Abstract

Cells of two molecular genetic types of breast cancer—hormone-dependent breast cancer (ZR-75 cell line) and triple-negative breast cancer (BT-20 cell line)—were studied using atomic force microscopy and an optical nanomotion detection method. Using the Peak Force QNM and Force Volume AFM modes, we revealed the unique patterns of the dependence of Young’s modulus on the indentation depth for two cancer cell lines that correlate with the features of the spatial organization of the actin cytoskeleton. Within a 200–300 nm layer just under the cell membrane, BT-20 cells are stiffer than ZR-75 cells, whereas in deeper cell regions, Young’s modulus of ZR-75 cells exceeds that of BT-20 cells. Two cancer cell lines also displayed a difference in cell nanomotion dynamics upon exposure to cytochalasin D, a potent actin polymerization inhibitor. The drug strongly modified the nanomotion pattern of BT-20 cells, whereas it had almost no effect on the ZR-75 cells. We are confident that nanomotion monitoring and measurement of the stiffness of cancer cells at various indentation depths deserve further studies to obtain effective predictive parameters for use in clinical practice.

Funder

Belarusian Republican Foundation for Fundamental Research

SNSF

Publisher

MDPI AG

Subject

General Medicine

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