Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells

Abstract This work combines single cell Raman spectroscopy (RS) with group and basis restricted non-negative matrix factorisation (GBR-NMF) to identify individual biochemical changes associated with radiation exposure in three human cancer cell lines. The cell lines analysed were derived from lung (...

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Main Authors: Kirsty Milligan, Xinchen Deng, Phillip Shreeves, Ramie Ali-Adeeb, Quinn Matthews, Alexandre Brolo, Julian J. Lum, Jeffrey L. Andrews, Andrew Jirasek
Format: Article
Language:English
Published: Nature Portfolio 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-83343-5
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author Kirsty Milligan
Xinchen Deng
Phillip Shreeves
Ramie Ali-Adeeb
Quinn Matthews
Alexandre Brolo
Julian J. Lum
Jeffrey L. Andrews
Andrew Jirasek
author_facet Kirsty Milligan
Xinchen Deng
Phillip Shreeves
Ramie Ali-Adeeb
Quinn Matthews
Alexandre Brolo
Julian J. Lum
Jeffrey L. Andrews
Andrew Jirasek
author_sort Kirsty Milligan
collection DOAJ
description Abstract This work combines single cell Raman spectroscopy (RS) with group and basis restricted non-negative matrix factorisation (GBR-NMF) to identify individual biochemical changes associated with radiation exposure in three human cancer cell lines. The cell lines analysed were derived from lung (H460), breast (MCF7) and prostate (LNCaP) tissue and are known to display varying degrees of radio sensitivity due to the inherent properties of each cell type. The GBR-NMF approach involves the deconstruction of Raman spectra into component biochemical bases using a library of Raman spectra of known biochemicals present in the cells. Subsequently, scores are obtained on each of these bases which can be directly correlated with the contribution of each chemical to the overall Raman spectrum. We validated GBR-NMF through the correlation of GBR-NMF-derived glycogen scores with scores that were previously observed using principal component analysis (PCA). Phosphatidylcholine, glucose, arginine and asparagine showed a distinct differential score pattern between radio-resistant and radio-sensitive cell types. In summary, the GBR-NMF approach allows for the monitoring of individual biochemical radiation-response dynamics previously unattainable with more traditional PCA-based approaches.
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spelling doaj.art-be7d93b845f34652a78ac742d2abbcae2022-12-21T21:52:15ZengNature PortfolioScientific Reports2045-23222021-02-0111111110.1038/s41598-021-83343-5Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cellsKirsty Milligan0Xinchen Deng1Phillip Shreeves2Ramie Ali-Adeeb3Quinn Matthews4Alexandre Brolo5Julian J. Lum6Jeffrey L. Andrews7Andrew Jirasek8Department of Physics, The University of British ColumbiaDepartment of Physics, The University of British ColumbiaDepartment of Statistics, The University of British ColumbiaDepartment of Physics, The University of British ColumbiaBC Cancer, Centre for the NorthDepartment of Chemistry, University of VictoriaDepartment of Biochemistry and Microbiology, University of VictoriaDepartment of Statistics, The University of British ColumbiaDepartment of Physics, The University of British ColumbiaAbstract This work combines single cell Raman spectroscopy (RS) with group and basis restricted non-negative matrix factorisation (GBR-NMF) to identify individual biochemical changes associated with radiation exposure in three human cancer cell lines. The cell lines analysed were derived from lung (H460), breast (MCF7) and prostate (LNCaP) tissue and are known to display varying degrees of radio sensitivity due to the inherent properties of each cell type. The GBR-NMF approach involves the deconstruction of Raman spectra into component biochemical bases using a library of Raman spectra of known biochemicals present in the cells. Subsequently, scores are obtained on each of these bases which can be directly correlated with the contribution of each chemical to the overall Raman spectrum. We validated GBR-NMF through the correlation of GBR-NMF-derived glycogen scores with scores that were previously observed using principal component analysis (PCA). Phosphatidylcholine, glucose, arginine and asparagine showed a distinct differential score pattern between radio-resistant and radio-sensitive cell types. In summary, the GBR-NMF approach allows for the monitoring of individual biochemical radiation-response dynamics previously unattainable with more traditional PCA-based approaches.https://doi.org/10.1038/s41598-021-83343-5
spellingShingle Kirsty Milligan
Xinchen Deng
Phillip Shreeves
Ramie Ali-Adeeb
Quinn Matthews
Alexandre Brolo
Julian J. Lum
Jeffrey L. Andrews
Andrew Jirasek
Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
Scientific Reports
title Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
title_full Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
title_fullStr Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
title_full_unstemmed Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
title_short Raman spectroscopy and group and basis-restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
title_sort raman spectroscopy and group and basis restricted non negative matrix factorisation identifies radiation induced metabolic changes in human cancer cells
url https://doi.org/10.1038/s41598-021-83343-5
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