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The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613834/ https://www.ncbi.nlm.nih.gov/pubmed/35962472 http://dx.doi.org/10.1002/1873-3468.14462 |
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author | Holzknecht, Max Guerrero‐Navarro, Lena Petit, Michele Albertini, Eva Damisch, Elisabeth Simonini, Anna Schmitt, Fernando Parson, Walther Fiegl, Heidelinde Weiss, Alexander Jansen‐Duerr, Pidder |
author_facet | Holzknecht, Max Guerrero‐Navarro, Lena Petit, Michele Albertini, Eva Damisch, Elisabeth Simonini, Anna Schmitt, Fernando Parson, Walther Fiegl, Heidelinde Weiss, Alexander Jansen‐Duerr, Pidder |
author_sort | Holzknecht, Max |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7613834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76138342022-11-16 The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro Holzknecht, Max Guerrero‐Navarro, Lena Petit, Michele Albertini, Eva Damisch, Elisabeth Simonini, Anna Schmitt, Fernando Parson, Walther Fiegl, Heidelinde Weiss, Alexander Jansen‐Duerr, Pidder FEBS Lett Research Articles 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. John Wiley and Sons Inc. 2022-08-12 2022-11 /pmc/articles/PMC7613834/ /pubmed/35962472 http://dx.doi.org/10.1002/1873-3468.14462 Text en © 2022 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Holzknecht, Max Guerrero‐Navarro, Lena Petit, Michele Albertini, Eva Damisch, Elisabeth Simonini, Anna Schmitt, Fernando Parson, Walther Fiegl, Heidelinde Weiss, Alexander Jansen‐Duerr, Pidder The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro |
title | The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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title_full | The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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title_fullStr | The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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title_full_unstemmed | The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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title_short | The mitochondrial enzyme FAHD1 regulates complex II activity in breast cancer cells and is indispensable for basal BT‐20 cells in vitro
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title_sort | mitochondrial enzyme fahd1 regulates complex ii activity in breast cancer cells and is indispensable for basal bt‐20 cells in vitro |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613834/ https://www.ncbi.nlm.nih.gov/pubmed/35962472 http://dx.doi.org/10.1002/1873-3468.14462 |
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