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  1. Article ; Online: Functional and multi-omics signatures of mitapivat efficacy upon activation of pyruvate kinase in red blood cells from patients with sickle cell disease.

    D'Alessandro, Angelo / Le, Kang / Lundt, Maureen / Li, Quan / Dunkelberger, Emily B / Cellmer, Troy / Worth, Andrew J / Patil, Spurthi / Huston, Chris / Grier, Abby / Dzieciatkowska, Monika / Stephenson, Daniel / Eaton, William A / Thein, Swee Lay

    Haematologica

    2024  

    Abstract: Mitapivat, a pyruvate kinase (PK) activator, shows great potential as a sickle cell disease (SCD)- modifying therapy. Safety and efficacy of mitapivat as a long-term maintenance therapy is currently being evaluated in two open-label studies. Here we ... ...

    Abstract Mitapivat, a pyruvate kinase (PK) activator, shows great potential as a sickle cell disease (SCD)- modifying therapy. Safety and efficacy of mitapivat as a long-term maintenance therapy is currently being evaluated in two open-label studies. Here we apply a comprehensive multi-omics approach to investigate the impact of activating PK on red blood cells (RBCs) from 15 SCD patients. HbSS patients were enrolled in one of the open label, extended studies (NCT04610866). Leuko-depleted RBCs obtained from fresh whole blood at baseline (visit 1, V1), prior to drug initiation and longitudinal time points over the course of the study were processed for multiomics through a stepwise extraction of metabolites, lipids and proteins. Mitapivat therapy had significant effects on the metabolome, lipidome and proteome of SCD RBCs. Mitapivat decreased 2,3-diphosphoglycerate (DPG) levels, increased adenosine triphosphate (ATP) levels, and improved hematologic and sickling parameters in patients with SCD. Agreement between omics measurements and clinical measurements confirmed the specificity of mitapivat on targeting late glycolysis, with glycolytic metabolites ranking as the top correlates to parameters of hemoglobin S (HbS) oxygen affinity (p50) and sickling kinetics (t50) during treatment. Mitapivat markedly reduced levels of proteins of mitochondrial origin within 2 weeks of initiation of drug treatment, with minimal changes in the reticulocyte counts. The first six months of treatment also witnessed transient elevation of lysophosphatidylcholines and oxylipins with depletion in free fatty acids, suggestive of an effect on membrane lipid remodeling. Multi-omics analysis of RBCs identified benefits for glycolysis, as well as activation of the Lands cycle.
    Language English
    Publishing date 2024-03-07
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    DOI 10.3324/haematol.2023.284831
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Metabolic rewiring induced by ranolazine improves melanoma responses to targeted therapy and immunotherapy.

    Redondo-Muñoz, Marta / Rodriguez-Baena, Francisco Javier / Aldaz, Paula / Caballé-Mestres, Adriá / Moncho-Amor, Verónica / Otaegi-Ugartemendia, Maddalen / Carrasco-Garcia, Estefania / Olias-Arjona, Ana / Lasheras-Otero, Irene / Santamaria, Eva / Bocanegra, Ana / Chocarro, Luisa / Grier, Abby / Dzieciatkowska M, Monika / Bigas, Claudia / Martin, Josefina / Urdiroz-Urricelqui, Uxue / Marzo, Florencio / Santamaria, Enrique /
    Kochan, Grazyna / Escors, David / Larrayoz, Ignacio Marcos / Heyn, Holger / D'Alessandro, Angelo / Attolini, Camille Stephan-Otto / Matheu, Ander / Wellbrock, Claudia / Benitah, Salvador Aznar / Sanchez-Laorden, Berta / Arozarena, Imanol

    Nature metabolism

    2023  Volume 5, Issue 9, Page(s) 1544–1562

    Abstract: Resistance of melanoma to targeted therapy and immunotherapy is linked to metabolic rewiring. Here, we show that increased fatty acid oxidation (FAO) during prolonged BRAF inhibitor (BRAFi) treatment contributes to acquired therapy resistance in mice. ... ...

    Abstract Resistance of melanoma to targeted therapy and immunotherapy is linked to metabolic rewiring. Here, we show that increased fatty acid oxidation (FAO) during prolonged BRAF inhibitor (BRAFi) treatment contributes to acquired therapy resistance in mice. Targeting FAO using the US Food and Drug Administration-approved and European Medicines Agency-approved anti-anginal drug ranolazine (RANO) delays tumour recurrence with acquired BRAFi resistance. Single-cell RNA-sequencing analysis reveals that RANO diminishes the abundance of the therapy-resistant NGFR
    MeSH term(s) United States ; Animals ; Mice ; Ranolazine/pharmacology ; Ranolazine/therapeutic use ; Melanoma/drug therapy ; Melanoma/metabolism ; Immunotherapy ; Protein Kinase Inhibitors/pharmacology ; Methionine
    Chemical Substances Ranolazine (A6IEZ5M406) ; Protein Kinase Inhibitors ; Methionine (AE28F7PNPL)
    Language English
    Publishing date 2023-08-10
    Publishing country Germany
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 2522-5812
    ISSN (online) 2522-5812
    DOI 10.1038/s42255-023-00861-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Simultaneous targeting of PD-1 and IL-2Rβγ with radiation therapy inhibits pancreatic cancer growth and metastasis.

    Piper, Miles / Hoen, Maureen / Darragh, Laurel B / Knitz, Michael W / Nguyen, Diemmy / Gadwa, Jacob / Durini, Greta / Karakoc, Idil / Grier, Abby / Neupert, Brooke / Van Court, Benjamin / Abdelazeem, Khalid N M / Yu, Justin / Olimpo, Nicholas A / Corbo, Sophia / Ross, Richard Blake / Pham, Tiffany T / Joshi, Molishree / Kedl, Ross M /
    Saviola, Anthony J / Amann, Maria / Umaña, Pablo / Codarri Deak, Laura / Klein, Christian / D'Alessandro, Angelo / Karam, Sana D

    Cancer cell

    2023  Volume 41, Issue 5, Page(s) 950–969.e6

    Abstract: In pancreatic ductal adenocarcinoma (PDAC) patients, we show that response to radiation therapy (RT) is characterized by increased IL-2Rβ and IL-2Rγ along with decreased IL-2Rα expression. The bispecific PD1-IL2v is a PD-1-targeted IL-2 variant (IL-2v) ... ...

    Abstract In pancreatic ductal adenocarcinoma (PDAC) patients, we show that response to radiation therapy (RT) is characterized by increased IL-2Rβ and IL-2Rγ along with decreased IL-2Rα expression. The bispecific PD1-IL2v is a PD-1-targeted IL-2 variant (IL-2v) immunocytokine with engineered IL-2 cis targeted to PD-1 and abolished IL-2Rα binding, which enhances tumor-antigen-specific T cell activation while reducing regulatory T cell (Treg) suppression. Using PD1-IL2v in orthotopic PDAC KPC-driven tumor models, we show marked improvement in local and metastatic survival, along with a profound increase in tumor-infiltrating CD8
    MeSH term(s) Humans ; CD8-Positive T-Lymphocytes ; Programmed Cell Death 1 Receptor ; Interleukin-2 Receptor alpha Subunit/therapeutic use ; Interleukin-2/pharmacology ; Pancreatic Neoplasms/genetics ; Pancreatic Neoplasms/radiotherapy ; Pancreatic Neoplasms/metabolism ; Carcinoma, Pancreatic Ductal/genetics ; Carcinoma, Pancreatic Ductal/radiotherapy ; Carcinoma, Pancreatic Ductal/drug therapy ; Immunotherapy
    Chemical Substances Programmed Cell Death 1 Receptor ; Interleukin-2 Receptor alpha Subunit ; Interleukin-2
    Language English
    Publishing date 2023-04-27
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2078448-X
    ISSN 1878-3686 ; 1535-6108
    ISSN (online) 1878-3686
    ISSN 1535-6108
    DOI 10.1016/j.ccell.2023.04.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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