| |  Online-Ressource |
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| Verfasst von: | Darawshi, Odai [VerfasserIn]  |
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| | Muz, Barbara [VerfasserIn] |
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| | Naamat, Shiri Gershon [VerfasserIn] |
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| | Praveen, Bellam [VerfasserIn] |
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| | Mahameed, Mohamed [VerfasserIn] |
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| | Goldberg, Karin [VerfasserIn] |
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| | Dipta, Priya [VerfasserIn] |
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| | Shmuel, Miriam [VerfasserIn] |
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| | Forno, Francesca [VerfasserIn] |
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| | Boukeileh, Shatha [VerfasserIn] |
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| | Pahima, Hadas [VerfasserIn] |
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| | Hermann, Julia [VerfasserIn] |
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| | Raab, Marc-Steffen [VerfasserIn] |
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| | Poos, Alexandra [VerfasserIn] |
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| | Weinhold, Niels [VerfasserIn] |
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| | Rosenbluh, Chaggai [VerfasserIn] |
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| | Gatt, Moshe E. [VerfasserIn] |
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| | Palm, Wilhelm [VerfasserIn] |
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| | Azab, Abdel Kareem [VerfasserIn] |
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| | Tirosh, Boaz [VerfasserIn] |
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| Titel: | An mTORC1 to HRI signaling axis promotes cytotoxicity of proteasome inhibitors in multiple myeloma |
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| Verf.angabe: | Odai Darawshi, Barbara Muz, Shiri Gershon Naamat, Bellam Praveen, Mohamed Mahameed, Karin Goldberg, Priya Dipta, Miriam Shmuel, Francesca Forno, Shatha Boukeileh, Hadas Pahima, Julia Hermann, Marc S. Raab, Alexandra M. Poos, Niels Weinhold, Chaggai Rosenbluh, Moshe E. Gatt, Wilhelm Palm, Abdel Kareem Azab and Boaz Tirosh |
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| E-Jahr: | 2022 |
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| Jahr: | 18 November 2022 |
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| Umfang: | 12 S. |
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| Fussnoten: | Gesehen am 18.01.2023 |
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| Titel Quelle: | Enthalten in: Cell death & disease |
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| Ort Quelle: | London [u.a.] : Nature Publishing Group, 2010 |
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| Jahr Quelle: | 2022 |
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| Band/Heft Quelle: | 13(2022), 11, Artikel-ID 969, Seite 1-12 |
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| ISSN Quelle: | 2041-4889 |
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| Abstract: | Multiple myeloma (MM) causes approximately 20% of deaths from blood cancers. Notwithstanding significant therapeutic progress, such as with proteasome inhibitors (PIs), MM remains incurable due to the development of resistance. mTORC1 is a key metabolic regulator, which frequently becomes dysregulated in cancer. While mTORC1 inhibitors reduce MM viability and synergize with other therapies in vitro, clinically, mTORC1 inhibitors are not effective for MM. Here we show that the inactivation of mTORC1 is an intrinsic response of MM to PI treatment. Genetically enforced hyperactivation of mTORC1 in MM was sufficient to compromise tumorigenicity in mice. In vitro, mTORC1-hyperactivated MM cells gained sensitivity to PIs and hypoxia. This was accompanied by increased mitochondrial stress and activation of the eIF2α kinase HRI, which initiates the integrated stress response. Deletion of HRI elevated the toxicity of PIs in wt and mTORC1-activated MM. Finally, we identified the drug PMA as a robust inducer of mTORC1 activity, which synergized with PIs in inducing MM cell death. These results help explain the clinical inefficacy of mTORC1 inhibitors in MM. Our data implicate mTORC1 induction and/or HRI inhibition as pharmacological strategies to enhance MM therapy by PIs. |
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| DOI: | doi:10.1038/s41419-022-05421-4 |
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| URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext: https://doi.org/10.1038/s41419-022-05421-4 |
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| | Volltext: https://www.nature.com/articles/s41419-022-05421-4 |
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| | DOI: https://doi.org/10.1038/s41419-022-05421-4 |
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| Datenträger: | Online-Ressource |
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| Sprache: | eng |
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| Sach-SW: | Apoptosis |
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| | Cancer metabolism |
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| K10plus-PPN: | 1831418835 |
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| Verknüpfungen: | → Zeitschrift |
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¬An¬ mTORC1 to HRI signaling axis promotes cytotoxicity of proteasome inhibitors in multiple myeloma / Darawshi, Odai [VerfasserIn]; 18 November 2022 (Online-Ressource)
