Atomic force microscopy as a tool for assessing the cellular elasticity and adhesiveness to identify cancer cells and tissues

被引:99
作者
Zemla, Joanna [1 ]
Danilkiewicz, Joanna [1 ]
Orzechowska, Barbara [1 ]
Pabijan, Joanna [1 ]
Seweryn, Sara [1 ]
Lekka, Malgorzata [1 ]
机构
[1] Polish Acad Sci, Inst Nucl Phys, Dept Biophys Microstruct, PL-31342 Krakow, Poland
关键词
Atomic force microscopy; Single molecule force spectroscopy; Single cell force spectroscopy; Single cell elasticity; Single molecule unbinding force; Quantitative characterization of cancer-related changes; MECHANICAL-PROPERTIES; OPTICAL TWEEZERS; CARCINOMA-CELLS; ADHESION; AFM; TUMOR; SPECTROSCOPY; INDENTATION; FIBROBLASTS; STIFFNESS;
D O I
10.1016/j.semcdb.2017.06.029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
From the first experiments of the atomic force microscopy (AFM) with biological samples, the range of its potential applications grows extensively. One of them is the use of AFM to characterize biophysical fingerprints of cancer progression in search of non-labelled biomarkers of the disease. The technique offers various functionalities, starting from surface imaging to detection of interaction forces, delivering quantitative parameters that can describe changes characteristic for various diseases, including cancer. In this review, the special emphasis was laid on these studies that compare the AFM-derived properties of reference and cancerous cells using all functionalities from cellular deformability measurements to quantification of the interaction forces at the single-molecule and single-cell levels. Despite the large effort and evidence of the microscope applicability to detect pathologically altered cells, there are still practical challenges remained to be solved before AFM can be implemented for routine cancer tracking and diagnosis. To-date, the AFM can be used to achieve a better understanding of cancer-related processes and mechanisms that could be further employed to design high-resolution clinical assays in a quantitative way. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 124
页数:10
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