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  1. AU="Firl, Christina E M"
  2. AU="Davies, Jane" AU="Davies, Jane"
  3. AU="Srinivasan, Karpagam"
  4. AU="Pritam Banerjee"
  5. AU="Fried, Miriam"
  6. AU="Andita P. Newton"
  7. AU="Larsen, B. B."
  8. AU="McPheeters, D"

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  1. Article ; Online: Contribution of S100A4-expressing fibroblasts to anti-SSA/Ro-associated atrioventricular nodal calcification and soluble S100A4 as a biomarker of clinical severity.

    Firl, Christina E M / Halushka, Marc / Fraser, Nicola / Masson, Mala / Cuneo, Bettina F / Saxena, Amit / Clancy, Robert / Buyon, Jill

    Frontiers in immunology

    2023  Volume 14, Page(s) 1114808

    Abstract: Background: Fibrosis and dystrophic calcification disrupting conduction tissue architecture are histopathological lesions characterizing cardiac manifestations of neonatal lupus (cardiac-NL) associated with maternal anti-SSA/Ro antibodies.: Objectives! ...

    Abstract Background: Fibrosis and dystrophic calcification disrupting conduction tissue architecture are histopathological lesions characterizing cardiac manifestations of neonatal lupus (cardiac-NL) associated with maternal anti-SSA/Ro antibodies.
    Objectives: Increased appreciation of heterogeneity in fibroblasts encourages re-examination of existing models with the consideration of multiple fibroblast subtypes (and their unique functional differences) in mind. This study addressed fibroblast heterogeneity by examining expression of α-Smooth Muscle Actin (myofibroblasts) and of S100 Calcium-Binding Protein A4 (S100A4).
    Methods: Using a previously established model of rheumatic scarring/fibrosis
    Results: S100A4 immunostaining was observed in 4 cardiac-NL hearts with positional identity in the conduction system at regions of dystrophic calcification but not fibrotic zones, the latter containing only myofibroblasts.
    Conclusions: These findings position the S100A4
    MeSH term(s) Infant, Newborn ; Humans ; Heart Block/etiology ; Heart Block/pathology ; Heart ; Biomarkers ; Calcinosis ; Fibrosis ; Fibroblasts/metabolism ; S100 Calcium-Binding Protein A4/metabolism
    Chemical Substances Biomarkers ; S100A4 protein, human (142662-27-9) ; S100 Calcium-Binding Protein A4
    Language English
    Publishing date 2023-04-06
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1114808
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Cysteine depletion induces pancreatic tumor ferroptosis in mice.

    Badgley, Michael A / Kremer, Daniel M / Maurer, H Carlo / DelGiorno, Kathleen E / Lee, Ho-Joon / Purohit, Vinee / Sagalovskiy, Irina R / Ma, Alice / Kapilian, Jonathan / Firl, Christina E M / Decker, Amanda R / Sastra, Steve A / Palermo, Carmine F / Andrade, Leonardo R / Sajjakulnukit, Peter / Zhang, Li / Tolstyka, Zachary P / Hirschhorn, Tal / Lamb, Candice /
    Liu, Tong / Gu, Wei / Seeley, E Scott / Stone, Everett / Georgiou, George / Manor, Uri / Iuga, Alina / Wahl, Geoffrey M / Stockwell, Brent R / Lyssiotis, Costas A / Olive, Kenneth P

    Science (New York, N.Y.)

    2020  Volume 368, Issue 6486, Page(s) 85–89

    Abstract: Ferroptosis is a form of cell death that results from the catastrophic accumulation of lipid reactive oxygen species (ROS). Oncogenic signaling elevates lipid ROS production in many tumor types and is counteracted by metabolites that are derived from the ...

    Abstract Ferroptosis is a form of cell death that results from the catastrophic accumulation of lipid reactive oxygen species (ROS). Oncogenic signaling elevates lipid ROS production in many tumor types and is counteracted by metabolites that are derived from the amino acid cysteine. In this work, we show that the import of oxidized cysteine (cystine) via system x
    MeSH term(s) Animals ; Carcinoma, Pancreatic Ductal/metabolism ; Carcinoma, Pancreatic Ductal/pathology ; Cationic Amino Acid Transporter 1/genetics ; Cell Line, Tumor ; Cystathionine gamma-Lyase/administration & dosage ; Cystathionine gamma-Lyase/pharmacology ; Cysteine/deficiency ; Cystine/metabolism ; Ferroptosis/drug effects ; Ferroptosis/genetics ; Gene Deletion ; Humans ; Mice ; Mice, Mutant Strains ; Pancreatic Neoplasms/metabolism ; Pancreatic Neoplasms/pathology
    Chemical Substances Cationic Amino Acid Transporter 1 ; Slc7a1 protein, mouse ; Cystine (48TCX9A1VT) ; Cystathionine gamma-Lyase (EC 4.4.1.1) ; Cysteine (K848JZ4886)
    Language English
    Publishing date 2020-04-03
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.aaw9872
    Database MEDical Literature Analysis and Retrieval System OnLINE

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