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  1. Article ; Online: Inhibition of mitochondrial folate metabolism drives differentiation through mTORC1 mediated purine sensing.

    Zarou, Martha M / Rattigan, Kevin M / Sarnello, Daniele / Shokry, Engy / Dawson, Amy / Ianniciello, Angela / Dunn, Karen / Copland, Mhairi / Sumpton, David / Vazquez, Alexei / Helgason, G Vignir

    Nature communications

    2024  Volume 15, Issue 1, Page(s) 1931

    Abstract: Supporting cell proliferation through nucleotide biosynthesis is an essential requirement for cancer cells. Hence, inhibition of folate-mediated one carbon (1C) metabolism, which is required for nucleotide synthesis, has been successfully exploited in ... ...

    Abstract Supporting cell proliferation through nucleotide biosynthesis is an essential requirement for cancer cells. Hence, inhibition of folate-mediated one carbon (1C) metabolism, which is required for nucleotide synthesis, has been successfully exploited in anti-cancer therapy. Here, we reveal that mitochondrial folate metabolism is upregulated in patient-derived leukaemic stem cells (LSCs). We demonstrate that inhibition of mitochondrial 1C metabolism through impairment of de novo purine synthesis has a cytostatic effect on chronic myeloid leukaemia (CML) cells. Consequently, changes in purine nucleotide levels lead to activation of AMPK signalling and suppression of mTORC1 activity. Notably, suppression of mitochondrial 1C metabolism increases expression of erythroid differentiation markers. Moreover, we find that increased differentiation occurs independently of AMPK signalling and can be reversed through reconstitution of purine levels and reactivation of mTORC1. Of clinical relevance, we identify that combination of 1C metabolism inhibition with imatinib, a frontline treatment for CML patients, decreases the number of therapy-resistant CML LSCs in a patient-derived xenograft model. Our results highlight a role for folate metabolism and purine sensing in stem cell fate decisions and leukaemogenesis.
    MeSH term(s) Humans ; Mechanistic Target of Rapamycin Complex 1 ; AMP-Activated Protein Kinases ; Purines/therapeutic use ; Purine Nucleotides ; Leukemia, Myeloid ; Folic Acid/metabolism ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy
    Chemical Substances Mechanistic Target of Rapamycin Complex 1 (EC 2.7.11.1) ; AMP-Activated Protein Kinases (EC 2.7.11.31) ; Purines ; Purine Nucleotides ; Folic Acid (935E97BOY8)
    Language English
    Publishing date 2024-03-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-024-46114-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Arginine dependency is a therapeutically exploitable vulnerability in chronic myeloid leukaemic stem cells.

    Rattigan, Kevin M / Zarou, Martha M / Brabcova, Zuzana / Prasad, Bodhayan / Zerbst, Désirée / Sarnello, Daniele / Kalkman, Eric R / Ianniciello, Angela / Scott, Mary T / Dunn, Karen / Shokry, Engy / Sumpton, David / Copland, Mhairi / Tardito, Saverio / Vande Voorde, Johan / Mussai, Francis / Cheng, Paul / Helgason, G Vignir

    EMBO reports

    2023  Volume 24, Issue 10, Page(s) e56279

    Abstract: To fuel accelerated proliferation, leukaemic cells undergo metabolic deregulation, which can result in specific nutrient dependencies. Here, we perform an amino acid drop-out screen and apply pre-clinical models of chronic phase chronic myeloid leukaemia ...

    Abstract To fuel accelerated proliferation, leukaemic cells undergo metabolic deregulation, which can result in specific nutrient dependencies. Here, we perform an amino acid drop-out screen and apply pre-clinical models of chronic phase chronic myeloid leukaemia (CML) to identify arginine as a nutrient essential for primary human CML cells. Analysis of the Microarray Innovations in Leukaemia (MILE) dataset uncovers reduced ASS1 levels in CML compared to most other leukaemia types. Stable isotope tracing reveals repressed activity of all urea cycle enzymes in patient-derived CML CD34
    MeSH term(s) Humans ; Arginine/metabolism ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/metabolism ; Apoptosis ; Stem Cells/metabolism ; Neoplastic Stem Cells/metabolism
    Chemical Substances Arginine (94ZLA3W45F)
    Language English
    Publishing date 2023-07-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2020896-0
    ISSN 1469-3178 ; 1469-221X
    ISSN (online) 1469-3178
    ISSN 1469-221X
    DOI 10.15252/embr.202256279
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Pyruvate anaplerosis is a targetable vulnerability in persistent leukaemic stem cells.

    Rattigan, Kevin M / Brabcova, Zuzana / Sarnello, Daniele / Zarou, Martha M / Roy, Kiron / Kwan, Ryan / de Beauchamp, Lucie / Dawson, Amy / Ianniciello, Angela / Khalaf, Ahmed / Kalkman, Eric R / Scott, Mary T / Dunn, Karen / Sumpton, David / Michie, Alison M / Copland, Mhairi / Tardito, Saverio / Gottlieb, Eyal / Vignir Helgason, G

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 4634

    Abstract: Deregulated oxidative metabolism is a hallmark of leukaemia. While tyrosine kinase inhibitors (TKIs) such as imatinib have increased survival of chronic myeloid leukaemia (CML) patients, they fail to eradicate disease-initiating leukemic stem cells (LSCs) ...

    Abstract Deregulated oxidative metabolism is a hallmark of leukaemia. While tyrosine kinase inhibitors (TKIs) such as imatinib have increased survival of chronic myeloid leukaemia (CML) patients, they fail to eradicate disease-initiating leukemic stem cells (LSCs). Whether TKI-treated CML LSCs remain metabolically deregulated is unknown. Using clinically and physiologically relevant assays, we generate multi-omics datasets that offer unique insight into metabolic adaptation and nutrient fate in patient-derived CML LSCs. We demonstrate that LSCs have increased pyruvate anaplerosis, mediated by increased mitochondrial pyruvate carrier 1/2 (MPC1/2) levels and pyruvate carboxylase (PC) activity, in comparison to normal counterparts. While imatinib reverses BCR::ABL1-mediated LSC metabolic reprogramming, stable isotope-assisted metabolomics reveals that deregulated pyruvate anaplerosis is not affected by imatinib. Encouragingly, genetic ablation of pyruvate anaplerosis sensitises CML cells to imatinib. Finally, we demonstrate that MSDC-0160, a clinical orally-available MPC1/2 inhibitor, inhibits pyruvate anaplerosis and targets imatinib-resistant CML LSCs in robust pre-clinical CML models. Collectively these results highlight pyruvate anaplerosis as a persistent and therapeutically targetable vulnerability in imatinib-treated CML patient-derived samples.
    MeSH term(s) Humans ; Pyruvic Acid ; Imatinib Mesylate/pharmacology ; Imatinib Mesylate/therapeutic use ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics ; Acclimatization ; Biological Assay
    Chemical Substances Pyruvic Acid (8558G7RUTR) ; Imatinib Mesylate (8A1O1M485B)
    Language English
    Publishing date 2023-08-17
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-40222-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Th17 cell master transcription factor RORC2 regulates HIV-1 gene expression and viral outgrowth.

    Wiche Salinas, Tomas Raul / Zhang, Yuwei / Sarnello, Daniele / Zhyvoloup, Alexander / Marchand, Laurence Raymond / Fert, Augustine / Planas, Delphine / Lodha, Manivel / Chatterjee, Debashree / Karwacz, Katarzyna / Oxenford, Sally / Routy, Jean-Pierre / Irlbeck, David / Amrine-Madsen, Heather / Ancuta, Petronela / Fassati, Ariberto

    Proceedings of the National Academy of Sciences of the United States of America

    2022  Volume 118, Issue 48

    Abstract: ... Among ... ...

    Abstract Among CD4
    MeSH term(s) Adult ; CD4-Positive T-Lymphocytes/immunology ; Cell Differentiation/immunology ; Cytokines/metabolism ; Female ; Gene Expression/genetics ; Gene Expression Regulation, Viral/genetics ; HIV Infections/immunology ; HIV-1/genetics ; HIV-1/growth & development ; Humans ; Lymphocyte Activation ; Male ; Middle Aged ; Nuclear Receptor Subfamily 1, Group F, Member 3/genetics ; Nuclear Receptor Subfamily 1, Group F, Member 3/metabolism ; Primary Cell Culture ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes, Regulatory/immunology ; Th17 Cells/metabolism ; Th17 Cells/physiology ; Transcription Factors/metabolism ; Viremia/immunology ; Viremia/virology ; Virus Replication/physiology
    Chemical Substances Cytokines ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; RORC protein, human ; Transcription Factors
    Language English
    Publishing date 2022-01-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2105927118
    Database MEDical Literature Analysis and Retrieval System OnLINE

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