Intact-Cell MALDI-ToF Mass Spectrometry for the Authentication of Drug-Adapted Cancer Cell Lines.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
02 10 2019
Historique:
received: 06 08 2019
revised: 22 09 2019
accepted: 27 09 2019
entrez: 5 10 2019
pubmed: 5 10 2019
medline: 14 8 2020
Statut: epublish

Résumé

The use of cell lines in research can be affected by cell line misidentification. Short tandem repeat (STR) analysis is an effective method, and the gold standard, for the identification of the genetic origin of a cell line, but methods that allow the discrimination between cell lines of the same genetic origin are lacking. Here, we use intact cell MALDI-ToF mass spectrometry analysis, routinely used for the identification of bacteria in clinical diagnostic procedures, for the authentication of a set of cell lines consisting of three parental neuroblastoma cell lines (IMR-5, IMR-32 and UKF-NB-3) and eleven drug-adapted sublines. Principal component analysis (PCA) of intact-cell MALDI-ToF mass spectrometry data revealed clear differences between most, but not all, of the investigated cell lines. Mass spectrometry whole-cell fingerprints enabled the separation of IMR-32 and its clonal subline IMR-5. Sublines that had been adapted to closely related drugs, for example, the cisplatin- and oxaliplatin-resistant UKF-NB-3 sublines and the vincristine- and vinblastine-adapted IMR-5 sublines, also displayed clearly distinctive patterns. In conclusion, intact whole-cell MALDI-ToF mass spectrometry has the potential to be further developed into an authentication method for mammalian cells of a common genetic origin.

Identifiants

pubmed: 31581737
pii: cells8101194
doi: 10.3390/cells8101194
pmc: PMC6830094
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Vincristine 5J49Q6B70F
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/K017640/1
Pays : United Kingdom

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Auteurs

Jane F Povey (JF)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. J.Povey@kent.ac.uk.

Emily Saintas (E)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. esaintas@icloud.com.

Adewale V Aderemi (AV)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. walerem@yahoo.com.

Florian Rothweiler (F)

Institut für Medizinische Virologie, Klinikum der Goethe-Universität, 60596 Frankfurt am Main, Germany. f.rothweiler@kinderkrebsstiftung-frankfurt.de.

Richard Zehner (R)

Institut für Rechtsmedizin, Klinikum der Goethe-Universität, 60596 Frankfurt am Main, Germany. zehner@em.uni-frankfurt.de.

Wilhelm G Dirks (WG)

Leibniz-Institute Deutsche Sammlung für Mikroorganismen und Zellkulturen GmbH, 38124 Braunschweig, Germany. wdi@dsmz.de.

Jindrich Cinatl (J)

Institut für Medizinische Virologie, Klinikum der Goethe-Universität, 60596 Frankfurt am Main, Germany.

Andrew J Racher (AJ)

Lonza Biologics, Slough SL1 4DX, UK. andy.racher@lonza.com.

Mark N Wass (MN)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. m.n.wass@kent.ac.uk.

C Mark Smales (CM)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. C.M.Smales@kent.ac.uk.

Martin Michaelis (M)

Industry Biotechnology Centre and School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK. M.Michaelis@kent.ac.uk.

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Classifications MeSH