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Integrated Metabolomics and Transcriptomics Using an Optimised Dual Extraction Process to Study Human Brain Cancer Cells and Tissues

Rahman, Ruman; Woodward, Alison; Pandele, Alina; Abdelrazig, Salah; Ortori, Catherine; Khan, Iqbal; Castellanos-Uribe, Marcos; May, Sean; Barrett, David; Grundy, Richard; Kim, Dong-Hyun

Integrated Metabolomics and Transcriptomics Using an Optimised Dual Extraction Process to Study Human Brain Cancer Cells and Tissues Thumbnail


Authors

Alina Pandele

Salah Abdelrazig

Catherine Ortori

Iqbal Khan

Marcos Castellanos-Uribe

David Barrett

RICHARD GRUNDY richard.grundy@nottingham.ac.uk
Professor of Paediatric Neuro-Oncology



Abstract

The integration of untargeted metabolomics and transcriptomics from the same population of cells or tissue enhances the confidence in the identified metabolic pathways and understanding of the enzyme–metabolite relationship. Here, we optimised a simultaneous extraction method of metabolites/lipids and RNA from ependymoma cells (BXD-1425). Relative to established RNA (mirVana kit) or metabolite (sequential solvent addition and shaking) single extraction methods, four dual-extraction techniques were evaluated and compared (methanol:water:chloroform ratios): cryomill/mirVana (1:1:2); cryomill-wash/Econospin (5:1:2); rotation/phenol-chloroform (9:10:1); Sequential/mirVana (1:1:3). All methods extracted the same metabolites, yet rotation/phenol-chloroform did not extract lipids. Cryomill/mirVana and sequential/mirVana recovered the highest amounts of RNA, at 70 and 68% of that recovered with mirVana kit alone. sequential/mirVana, involving RNA extraction from the interphase of our established sequential solvent addition and shaking metabolomics-lipidomics extraction method, was the most efficient approach overall. Sequential/mirVana was applied to study a) the biological effect caused by acute serum starvation in BXD-1425 cells and b) primary ependymoma tumour tissue. We found (a) 64 differentially abundant metabolites and 28 differentially expressed metabolic genes, discovering four gene-metabolite interactions, and (b) all metabolites and 62% lipids were above the limit of detection, and RNA yield was sufficient for transcriptomics, in just 10 mg of tissue.

Citation

Rahman, R., Woodward, A., Pandele, A., Abdelrazig, S., Ortori, C., Khan, I., …Kim, D. (2021). Integrated Metabolomics and Transcriptomics Using an Optimised Dual Extraction Process to Study Human Brain Cancer Cells and Tissues. Metabolites, 11(4), Article 240. https://doi.org/10.3390/metabo11040240

Journal Article Type Article
Acceptance Date Apr 12, 2021
Online Publication Date Apr 14, 2021
Publication Date 2021-04
Deposit Date Apr 13, 2021
Publicly Available Date Apr 20, 2021
Journal Metabolites
Electronic ISSN 2218-1989
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 11
Issue 4
Article Number 240
DOI https://doi.org/10.3390/metabo11040240
Keywords Biochemistry; Molecular Biology; Endocrinology, Diabetes and Metabolism
Public URL https://nottingham-repository.worktribe.com/output/5461719
Publisher URL https://www.mdpi.com/2218-1989/11/4/240