Analysis of phosphatidylcholines alterations in human glioblastoma multiform tissues ex vivo

   
Pekov S.I.1, Sorokin A.A.2, Kuzin A.A.2, Bocharov K.V.3, Bormotov D.S.2, Shivalin A.S.2, Shurkhay V.A.4, Potapov A.A.5, Nikolaev E.N.6, Popov I.A.2

1. Skolkovo Institute of Science and Technology, Moscow, Russia; Moscow Institute of Physics and Technology (National Research University), Moscow, Russia
2. Moscow Institute of Physics and Technology (National Research University), Moscow, Russia
3. Semenov Federal Center of Chemical Physic of RAS, Moscow, Russia
4. Moscow Institute of Physics and Technology (National Research University), Moscow, Russia; N.N. Burdenko National Medical Research Center of Neurosurgery, Moscow, Russia
5. N.N. Burdenko National Medical Research Center of Neurosurgery, Moscow, Russia
6. Skolkovo Institute of Science and Technology, Moscow, Russia
Section: Clinical and Diagnostic Research
DOI: 10.18097/PBMC20216701081      PubMed Id: 33645525
Year: 2021  Volume: 67  Issue: 1  Pages: 81-87
Significant metabolism alteration is accompanying the cell malignization process. Energy metabolism disturbance leads to the activation of de novo synthesis and beta-oxidation processes of lipids and fatty acids in a cancer cell, which becomes an indicator of pathological processes inside the cell. The majority of studies dealing with lipid metabolism alterations in glial tumors are performed using the cell lines in vitro or animal models. However, such conditions do not entirely represent the physiological conditions of cell growth or possible cells natural variability. This work presents the results of the data obtained by applying ambient mass spectrometry to human glioblastoma multiform tissues. By analyzing a relatively large cohort of primary and secondary glioblastoma samples, we identify the alterations in cells lipid composition, which accompanied the development of grade IV brain tumors. We demonstrate that primary glioblastomas, as well as ones developed from astrocytomas, are enriched with mono- and diunsaturated phosphatidylcholines (PC 26:1, 30:2, 32:1, 32:2, 34:1, 34:2). Simultaneously, the saturated and polyunsaturated phosphatidylcholines and phosphatidylethanolamines decrease. These alterations are obviously linked to the availability of the polyunsaturated fatty acids and activation of the de novo lipid synthesis and beta-oxidation pathways under the anaerobic conditions in the tumor core.
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Keywords: mass spectrometry, lipidomics, metabolomics, glioblastoma multiform
Citation:

Pekov, S. I., Sorokin, A. A., Kuzin, A. A., Bocharov, K. V., Bormotov, D. S., Shivalin, A. S., Shurkhay, V. A., Potapov, A. A., Nikolaev, E. N., Popov, I. A. (2021). Analysis of phosphatidylcholines alterations in human glioblastoma multiform tissues ex vivo. Biomeditsinskaya Khimiya, 67(1), 81-87.
This paper is also available as the English translation: 10.1134/S1990750821030070
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