Search Results - "Soroko, Kara M"
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Combined targeting of the BRD4-NUT-p300 axis in NUT midline carcinoma by dual selective bromodomain inhibitor, NEO2734
Published in Molecular cancer therapeutics (01-07-2020)“…NUT midline carcinoma (NMC) is a rare, aggressive subtype of squamous carcinoma that is driven by the BRD4-NUT fusion oncoprotein. BRD4, a BET protein, binds…”
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Antigen presentation deficiency, mesenchymal differentiation, and resistance to immunotherapy in the murine syngeneic CT2A tumor model
Published in Frontiers in immunology (28-12-2023)“…The GL261 and CT2A syngeneic tumor lines are frequently used as immunocompetent orthotopic mouse models of human glioblastoma (huGBM) but demonstrate distinct…”
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Milademetan is a highly potent MDM2 inhibitor in Merkel cell carcinoma
Published in JCI insight (08-07-2022)“…Merkel cell carcinoma (MCC) is an aggressive neuroendocrine carcinoma of the skin with 2 etiologies. Merkel cell polyomavirus (MCPyV) integration is present in…”
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Concurrent Dexamethasone Limits the Clinical Benefit of Immune Checkpoint Blockade in Glioblastoma
Published in Clinical cancer research (01-01-2021)“…Dexamethasone, a uniquely potent corticosteroid, is frequently administered to patients with brain tumors to decrease tumor-associated edema, but limited data…”
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Quinazolinones as allosteric fourth-generation EGFR inhibitors for the treatment of NSCLC
Published in Bioorganic & medicinal chemistry letters (15-07-2022)“…[Display omitted] The C797S mutation confers resistance to covalent EGFR inhibitors used in the treatment of lung tumors with the activating L858R mutation…”
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ERK Inhibitor LY3214996-Based Treatment Strategies for RAS -Driven Lung Cancer
Published in Molecular cancer therapeutics (01-04-2021)“…gene mutations are the most frequent oncogenic event in lung cancer. They activate multiple RAS-centric signaling networks among them the MAPK, PI3K, and RB…”
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An allosteric inhibitor against the therapy-resistant mutant forms of EGFR in non-small cell lung cancer
Published in Nature cancer (01-04-2022)“…Epidermal growth factor receptor (EGFR) therapy using small-molecule tyrosine kinase inhibitors (TKIs) is initially efficacious in patients with EGFR-mutant…”
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Abstract P203: Milademetan is a potent, murine double minute 2 (MDM2) inhibitor, highly active in TP53 wild-type (p53WT) Merkel cell carcinoma (MCC) cell lines
Published in Molecular cancer therapeutics (01-12-2021)“…Abstract Background: MCC is a highly aggressive neuroendocrine carcinoma of the skin with a poor overall prognosis. Current treatment options include surgery…”
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Milademetan is a highly potent MDM2 inhibitor in TP53 wild-type (p53 WT) models of Merkel cell carcinoma (MCC)
Published in Journal of investigative dermatology (01-10-2022)Get full text
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Establishment of the Bcwm.2 Cell Line As a BTK-Inhibitor Resistant, BCL2 Inhibitor Sensitive in Vitro and In Vivo Study Model for Waldenström's Macroglobulinemia
Published in Blood (02-11-2023)“…Background: Waldenström's macroglobulinemia (WM) is an indolent B-cell lymphoproliferative disorder characterized by bone marrow (BM) infiltration with…”
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Allosteric inhibition of drug resistant forms of EGFR L858R mutant NSCLC
Published in Nature cancer (01-04-2022)“…Although treatment with small molecule epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) is initially efficacious for patients with…”
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