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Functional mitochondrial respiration is essential for glioblastoma tumour growth

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F25%3A00637936" target="_blank" >RIV/68378041:_____/25:00637936 - isvavai.cz</a>

  • Alternative codes found

    RIV/86652036:_____/25:00637936 RIV/68378050:_____/25:00637936 RIV/00216208:11110/25:10497830 RIV/00216208:11130/25:10497830 and 2 more

  • Result on the web

    <a href="https://www.nature.com/articles/s41388-025-03429-6" target="_blank" >https://www.nature.com/articles/s41388-025-03429-6</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41388-025-03429-6" target="_blank" >10.1038/s41388-025-03429-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Functional mitochondrial respiration is essential for glioblastoma tumour growth

  • Original language description

    Horizontal transfer of mitochondria from the tumour microenvironment to cancer cells to support proliferation and enhance tumour progression has been shown for various types of cancer in recent years. Glioblastoma, the most aggressive adult brain tumour, has proven to be no exception when it comes to dynamic intercellular mitochondrial movement, as shown in this study using an orthotopic tumour model of respiration-deficient glioblastoma cells. Although confirmed mitochondrial transfer was shown to facilitate tumour progression in glioblastoma, we decided to investigate whether the related electron transport chain recovery is necessary for tumour formation in the brain. Based on experiments using time-resolved analysis of tumour formation by glioblastoma cells depleted of their mitochondrial DNA, we conclude that functional mitochondrial respiration is essential for glioblastoma growth in vivo, because it is needed to support coenzyme Q redox cycling for de novo pyrimidine biosynthesis controlled by respiration-linked dihydroorotate dehydrogenase enzyme activity. We also demonstrate here that astrocytes are key mitochondrial donors in this model.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Oncogene

  • ISSN

    0950-9232

  • e-ISSN

    1476-5594

  • Volume of the periodical

    44

  • Issue of the periodical within the volume

    30

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    16

  • Pages from-to

    2588-2603

  • UT code for WoS article

    001481335300001

  • EID of the result in the Scopus database

    2-s2.0-105004356661