Pidder Jansen‐Duerr

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Articles (11)

The mitochondrial enzyme fumarylacetoacetate hydrolase domain‐containing protein 1 (FAHD1) was identified to be upregulated in breast cancer tissues. Here, we show that FAHD1 is indispensable for the survival of BT‐20 cells, representing the basal breast cancer cell type. A lentiviral knock‐down of FAHD1 in the breast cancer cell lines MCF‐7 and BT‐20 results in lower succinate dehydrogenase (complex II) activity. In luminal MCF‐7 cells, this leads to reduced proliferation when cultured in medium containing only glutamine as the carbon source. Of note, both cell lines show attenuated protein levels of the enzyme glutaminase (GLS) which activates programmed cell death in BT‐20. These findings demonstrate that FAHD1 is crucial for the functionality of complex II in breast cancer cells and acts on glutaminolysis in the mitochondria.

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

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2020

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2020

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2020

Collaborators (9)

Heidi Fiegl

Medical University of Innsbruck

AUSTRIA
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Corina T. Madreiter-Sokolowski

Associate Professor

Medical University of Graz

AUSTRIA
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Elisabeth Maria Damisch

Medical University of Innsbruck

AUSTRIA
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Thomas Haller

Assoc.-Prof.

Medical University of Innsbruck

AUSTRIA
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Klaus R. Liedl

University of Innsbruck

AUSTRIA
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Alexander Weiss

European Research Institute for the Biology of Ageing, University of Groningen, UMC Groningen: Groningen, Netherlands

AUSTRIA
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Maria Cavinato

-

AUSTRIA
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Frank Edenhofer

Prof., Head Dpt. Genomics, Stem Cell Biology & Regenerative Medicine

University of Innsbruck

AUSTRIA
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Marta Suarez Cubero

University of Innsbruck

AUSTRIA
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