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Coherent confocal light scattering spectroscopic microscopy evaluates cancer progression and aggressiveness in live cells and tissue.


ABSTRACT: The observation of biological structures in live cells beyond the diffraction limit with super-resolution fluorescence microscopy is limited by the ability of fluorescence probes to permeate live cells and the effect of these probes, which are often toxic, on cellular behavior. Here we present a coherent confocal light scattering and absorption spectroscopic microscopy that for the first time enables the use of large numerical aperture optics to characterize structures in live cells down to 10 nm spatial scales, well beyond the diffraction limit. Not only does this new capability allow high resolution microscopy with light scattering contrast, but it can also be used with almost any light scattering spectroscopic application which employs lenses. We demonstrate that the coherent light scattering contrast based technique allows continuous temporal tracking of the transition from non-cancerous to an early cancerous state in live cells, without exogenous markers. We also use the technique to sense differences in the aggressiveness of cancer in live cells and for label free identification of different grades of cancer in resected tumor tissues.

SUBMITTER: Pleskow DK 

PROVIDER: S-EPMC8411902 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Coherent confocal light scattering spectroscopic microscopy evaluates cancer progression and aggressiveness in live cells and tissue.

Pleskow Douglas K DK   Zhang Lei L   Turzhitsky Vladimir V   Coughlan Mark F MF   Khan Umar U   Zhang Xuejun X   Sheil Conor J CJ   Glyavina Maria M   Chen Liming L   Shinagare Shweta S   Zakharov Yuri N YN   Vitkin Edward E   Itzkan Irving I   Perelman Lev T LT   Qiu Le L  

ACS photonics 20210620 7


The observation of biological structures in live cells beyond the diffraction limit with super-resolution fluorescence microscopy is limited by the ability of fluorescence probes to permeate live cells and the effect of these probes, which are often toxic, on cellular behavior. Here we present a coherent confocal light scattering and absorption spectroscopic microscopy that for the first time enables the use of large numerical aperture optics to characterize structures in live cells down to 10 n  ...[more]

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