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A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data

BACKGROUND: Drug mass spectrometry imaging (MSI) data contain knowledge about drug and several other molecular ions present in a biological sample. However, a proper approach to fully explore the potential of such type of data is still missing. Therefore, a computational pipeline that combines diffe...

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Autores principales: Prasad, Mridula, Postma, Geert, Franceschi, Pietro, Morosi, Lavinia, Giordano, Silvia, Falcetta, Francesca, Giavazzi, Raffaella, Davoli, Enrico, Buydens, Lutgarde M C, Jansen, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688471/
https://www.ncbi.nlm.nih.gov/pubmed/33241286
http://dx.doi.org/10.1093/gigascience/giaa131
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author Prasad, Mridula
Postma, Geert
Franceschi, Pietro
Morosi, Lavinia
Giordano, Silvia
Falcetta, Francesca
Giavazzi, Raffaella
Davoli, Enrico
Buydens, Lutgarde M C
Jansen, Jeroen
author_facet Prasad, Mridula
Postma, Geert
Franceschi, Pietro
Morosi, Lavinia
Giordano, Silvia
Falcetta, Francesca
Giavazzi, Raffaella
Davoli, Enrico
Buydens, Lutgarde M C
Jansen, Jeroen
author_sort Prasad, Mridula
collection PubMed
description BACKGROUND: Drug mass spectrometry imaging (MSI) data contain knowledge about drug and several other molecular ions present in a biological sample. However, a proper approach to fully explore the potential of such type of data is still missing. Therefore, a computational pipeline that combines different spatial and non-spatial methods is proposed to link the observed drug distribution profile with tumor heterogeneity in solid tumor. Our data analysis steps include pre-processing of MSI data, cluster analysis, drug local indicators of spatial association (LISA) map, and ions selection. RESULTS: The number of clusters identified from different tumor tissues. The spatial homogeneity of the individual cluster was measured using a modified version of our drug homogeneity method. The clustered image and drug LISA map were simultaneously analyzed to link identified clusters with observed drug distribution profile. Finally, ions selection was performed using the spatially aware method. CONCLUSIONS: In this paper, we have shown an approach to correlate the drug distribution with spatial heterogeneity in untargeted MSI data. Our approach is freely available in an R package 'CorrDrugTumorMSI'.
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spelling pubmed-76884712020-12-07 A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data Prasad, Mridula Postma, Geert Franceschi, Pietro Morosi, Lavinia Giordano, Silvia Falcetta, Francesca Giavazzi, Raffaella Davoli, Enrico Buydens, Lutgarde M C Jansen, Jeroen Gigascience Research BACKGROUND: Drug mass spectrometry imaging (MSI) data contain knowledge about drug and several other molecular ions present in a biological sample. However, a proper approach to fully explore the potential of such type of data is still missing. Therefore, a computational pipeline that combines different spatial and non-spatial methods is proposed to link the observed drug distribution profile with tumor heterogeneity in solid tumor. Our data analysis steps include pre-processing of MSI data, cluster analysis, drug local indicators of spatial association (LISA) map, and ions selection. RESULTS: The number of clusters identified from different tumor tissues. The spatial homogeneity of the individual cluster was measured using a modified version of our drug homogeneity method. The clustered image and drug LISA map were simultaneously analyzed to link identified clusters with observed drug distribution profile. Finally, ions selection was performed using the spatially aware method. CONCLUSIONS: In this paper, we have shown an approach to correlate the drug distribution with spatial heterogeneity in untargeted MSI data. Our approach is freely available in an R package 'CorrDrugTumorMSI'. Oxford University Press 2020-11-25 /pmc/articles/PMC7688471/ /pubmed/33241286 http://dx.doi.org/10.1093/gigascience/giaa131 Text en © The Author(s) 2020. Published by Oxford University Press GigaScience. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Prasad, Mridula
Postma, Geert
Franceschi, Pietro
Morosi, Lavinia
Giordano, Silvia
Falcetta, Francesca
Giavazzi, Raffaella
Davoli, Enrico
Buydens, Lutgarde M C
Jansen, Jeroen
A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title_full A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title_fullStr A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title_full_unstemmed A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title_short A methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
title_sort methodological approach to correlate tumor heterogeneity with drug distribution profile in mass spectrometry imaging data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688471/
https://www.ncbi.nlm.nih.gov/pubmed/33241286
http://dx.doi.org/10.1093/gigascience/giaa131
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