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      Automated estimation of cancer cell deformability with machine learning and acoustic trapping

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          Abstract

          Cell deformability is a useful feature for diagnosing various diseases (e.g., the invasiveness of cancer cells). Existing methods commonly inflict pressure on cells and observe changes in cell areas, diameters, or thickness according to the degree of pressure. Then, the Young’s moduli (i.e., a measure of deformability) of cells are estimated based on the assumption that the degrees of the changes are inversely proportional to Young’s moduli. However, manual measurements of the physical changes in cells are labor-intensive, and the subjectivity of the operators can intervene during this step, thereby causing considerable uncertainty. Further, because the shapes of cells are nonuniform, we cannot ensure the assumption for linear correlations of physical changes in cells with their deformability. Therefore, this study aims at measuring non-linear elastic moduli of live cells (degrees of cell deformability) automatically by employing conventional neural networks (CNN) and multilayer perceptrons (MLP) while preserving (or enhancing) the accuracy of the manual methods. First, we obtain photomicrographs of cells on multiple pressure levels using single-beam acoustic tweezers, and then, we suggest an image preprocessing method for emphasizing changes in cell areas on the photomicrographs. The CNN model is trained to measure the ratios of the cell area change at each pressure level. Then, we apply the multilayer perceptron (MLP) to learn the correlations of the cell area change ratios according to the pressure levels with cell deformability. The accuracy of the CNN was evaluated using two types of breast cancer cells: MDA-MB-231 (invasive) and MCF-7 (noninvasive). The MLP was assessed using five different beads (Young’s moduli from 0.214 to 9.235 kPa), which provides standardized reference data of the non-linear elastic moduli of live cells. Finally, we validated the practicality of the proposed system by examining whether the non-linear elastic moduli estimated by the proposed system can distinguish invasive breast cancer cells from noninvasive ones.

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          Adaptive subgradient methods for online learning and stochastic optimization

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            The optical stretcher: a novel laser tool to micromanipulate cells.

            When a dielectric object is placed between two opposed, nonfocused laser beams, the total force acting on the object is zero but the surface forces are additive, thus leading to a stretching of the object along the axis of the beams. Using this principle, we have constructed a device, called an optical stretcher, that can be used to measure the viscoelastic properties of dielectric materials, including biologic materials such as cells, with the sensitivity necessary to distinguish even between different individual cytoskeletal phenotypes. We have successfully used the optical stretcher to deform human erythrocytes and mouse fibroblasts. In the optical stretcher, no focusing is required, thus radiation damage is minimized and the surface forces are not limited by the light power. The magnitude of the deforming forces in the optical stretcher thus bridges the gap between optical tweezers and atomic force microscopy for the study of biologic materials.
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              A comparison of methods to assess cell mechanical properties

              Cell mechanics controls important cellular and subcellular functions, including cell adhesion, migration, polarization, and differentiation, as well as organelle organization, and trafficking inside the cytoplasm. Yet, reported values of cell stiffness and viscosity vary strongly, suggesting disagreements in how results of different methods are obtained or analyzed. To address this issue and illustrate the complementarity of different instruments, we present, analyze, and critically compare measurements conducted by some of the most widely used methods of cell mechanics: atomic force microscopy, magnetic twisting cytometry, particle-tracking microrheology, parallel-plates rheometry, cell monolayer rheology, and the optical stretcher. These measurements highlight that elastic and viscous moduli of MCF-7 breast cancer cells can vary 1,000 fold and 100 fold, respectively. We discuss the sources of these variations, including the level of applied mechanical stress and rate of deformation, the geometry of the probe, the location probed in the cell, and the extracellular microenvironment.
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                Author and article information

                Contributors
                hglim@pknu.ac.kr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                27 April 2022
                27 April 2022
                2022
                : 12
                : 6891
                Affiliations
                [1 ]GRID grid.411947.e, ISNI 0000 0004 0470 4224, Department of Artificial Intelligence, , The Catholic University of Korea, ; Bucheon, 14662 Republic of Korea
                [2 ]GRID grid.412576.3, ISNI 0000 0001 0719 8994, Department of Biomedical Engineering, , Pukyong National University, ; Busan, 48513 Republic of Korea
                [3 ]GRID grid.42505.36, ISNI 0000 0001 2156 6853, Department of Biomedical Engineering, , University of Southern California, ; Los Angeles, CA 90089 USA
                [4 ]GRID grid.49100.3c, ISNI 0000 0001 0742 4007, Department of Convergence IT Engineering, , Pohang University of Science and Technology, ; Pohang, 37673 Republic of Korea
                Article
                10882
                10.1038/s41598-022-10882-w
                9046201
                35477742
                0e13f325-28e9-4e70-bcbe-f2391e4b6100
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 January 2022
                : 13 April 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100002648, Catholic University of Korea;
                Award ID: M-2021-B0008-00043
                Funded by: FundRef http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: 2021R1F1A1062979
                Award ID: 2019R1A2C2010484
                Funded by: Pukyong National University Research Fund
                Award ID: CD20210995
                Categories
                Article
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                © The Author(s) 2022

                Uncategorized
                biomedical engineering,cancer screening
                Uncategorized
                biomedical engineering, cancer screening

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