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1.
ACG Case Rep J ; 11(7): e01434, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38994190

ABSTRACT

Two major etiologies of hyperbilirubinemia include hemolysis and cholestasis. Although rare, the former can give rise to the latter through the formation of pigment gallstones and subsequent biliary tree obstruction. We report a case of a 57-year-old woman with systemic lupus erythematosus who presented with dyspnea and right upper quadrant abdominal pain. She was found to have hepatolithiasis and choledocholithiasis secondary to warm autoimmune hemolytic anemia in the setting of COVID-19. In patients with symptomatic anemia secondary to acute hemolysis and concomitant right upper quadrant abdominal pain, elevated hepatocellular laboratory results should prompt a high clinical suspicion for biliary tree pigment stones.

2.
Sci Rep ; 9(1): 19530, 2019 12 20.
Article in English | MEDLINE | ID: mdl-31863071

ABSTRACT

Triple-negative breast cancer (TNBC) is a highly aggressive subtype that is untreatable with hormonal or HER2-targeted therapies and is also typically unresponsive to checkpoint-blockade immunotherapy. Within the tumor microenvironment dysregulated immune cell metabolism has emerged as a key mechanism of tumor immune-evasion. We have discovered that the Liver-X-Receptors (LXRα and LXRß), nuclear receptors known to regulate lipid metabolism and tumor-immune interaction, are highly activated in TNBC tumor associated myeloid cells. We therefore theorized that inhibiting LXR would induce immune-mediated TNBC-tumor clearance. Here we show that pharmacological inhibition of LXR activity induces tumor destruction primarily through stimulation of CD8+ T-cell cytotoxic activity and mitochondrial metabolism. Our results imply that LXR inverse agonists may be a promising new class of TNBC immunotherapies.


Subject(s)
CD8-Positive T-Lymphocytes/metabolism , Triple Negative Breast Neoplasms/metabolism , Animals , Antineoplastic Agents/therapeutic use , CD8-Positive T-Lymphocytes/drug effects , Cell Line, Tumor , Female , Humans , Mice , Mice, Inbred C57BL , T-Lymphocytes, Cytotoxic/metabolism , Triple Negative Breast Neoplasms/immunology , Tumor Microenvironment/immunology , Tumor Microenvironment/physiology , Xenograft Model Antitumor Assays
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