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Author Details

Victoria M Richon
Discovery and Preclinical Sciences
1984
118
73
PMIDPaper TitleJournal TitlePublished Year
34375612PARP7 negatively regulates the type I interferon response in cancer cells and its inhibition triggers antitumor immunity.Cancer Cell2021
33705687A potent and selective PARP14 inhibitor decreases protumor macrophage gene expression and elicits inflammatory responses in tumor explants.Cell Chem Biol2021
34375612PARP7 negatively regulates the type I interferon response in cancer cells and its inhibition triggers antitumor immunity.Cancer Cell2021
33705687A potent and selective PARP14 inhibitor decreases protumor macrophage gene expression and elicits inflammatory responses in tumor explants.Cell Chem Biol2021
28950000Glutaminase is essential for the growth of triple-negative breast cancer cells with a deregulated glutamine metabolism pathway and its suppression synergizes with mTOR inhibition.PLoS One2017
28950000Glutaminase is essential for the growth of triple-negative breast cancer cells with a deregulated glutamine metabolism pathway and its suppression synergizes with mTOR inhibition.PLoS One2017
26769278The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat.J Med Chem2016
26769278The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat.J Med Chem2016
25979925CCR 20th Anniversary Commentary: Vorinostat-Gateway to Epigenetic Therapy.Clin Cancer Res2015
25897982Redox-Mediated Suberoylanilide Hydroxamic Acid Sensitivity in Breast Cancer.Antioxid Redox Signal2015
26222556Structural Approaches to Cancer Drug Development.N Engl J Med2015
25979925CCR 20th Anniversary Commentary: Vorinostat-Gateway to Epigenetic Therapy.Clin Cancer Res2015
26222556Structural Approaches to Cancer Drug Development.N Engl J Med2015
25897982Redox-Mediated Suberoylanilide Hydroxamic Acid Sensitivity in Breast Cancer.Antioxid Redox Signal2015
24415392Nonclinical pharmacokinetics and metabolism of EPZ-5676, a novel DOT1L histone methyltransferase inhibitor.Biopharm Drug Dispos2014
24415392Nonclinical pharmacokinetics and metabolism of EPZ-5676, a novel DOT1L histone methyltransferase inhibitor.Biopharm Drug Dispos2014
24563539Selective inhibition of EZH2 by EPZ-6438 leads to potent antitumor activity in EZH2-mutant non-Hodgkin lymphoma.Mol Cancer Ther2014
24563539Selective inhibition of EZH2 by EPZ-6438 leads to potent antitumor activity in EZH2-mutant non-Hodgkin lymphoma.Mol Cancer Ther2014
23138183Abrogation of MLL-AF10 and CALM-AF10-mediated transformation through genetic inactivation or pharmacological inhibition of the H3K79 methyltransferase Dot1l.Leukemia2013
23801631Potent inhibition of DOT1L as treatment of MLL-fusion leukemia.Blood2013
24092806Molecular and biologic analysis of histone deacetylase inhibitors with diverse specificities.Mol Cancer Ther2013
24319157Drug discovery in rare indications: opportunities and challenges.Hematology Am Soc Hematol Educ Program2013
23361907Leukemic transformation by the MLL-AF6 fusion oncogene requires the H3K79 methyltransferase Dot1l.Blood2013
23138183Abrogation of MLL-AF10 and CALM-AF10-mediated transformation through genetic inactivation or pharmacological inhibition of the H3K79 methyltransferase Dot1l.Leukemia2013
23620515Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2.Proc Natl Acad Sci U S A2013
23160372Targeting genetic alterations in protein methyltransferases for personalized cancer therapeutics.Oncogene2013
24319157Drug discovery in rare indications: opportunities and challenges.Hematology Am Soc Hematol Educ Program2013
24092806Molecular and biologic analysis of histone deacetylase inhibitors with diverse specificities.Mol Cancer Ther2013
23620515Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2.Proc Natl Acad Sci U S A2013
23801631Potent inhibition of DOT1L as treatment of MLL-fusion leukemia.Blood2013
23160372Targeting genetic alterations in protein methyltransferases for personalized cancer therapeutics.Oncogene2013
23361907Leukemic transformation by the MLL-AF6 fusion oncogene requires the H3K79 methyltransferase Dot1l.Blood2013
22850114A687V EZH2 is a gain-of-function mutation found in lymphoma patients.FEBS Lett2012
22850114A687V EZH2 is a gain-of-function mutation found in lymphoma patients.FEBS Lett2012
22978415Conformational adaptation drives potent, selective and durable inhibition of the human protein methyltransferase DOT1L.Chem Biol Drug Des2012
23023262A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.Nat Chem Biol2012
23023262A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.Nat Chem Biol2012
22978415Conformational adaptation drives potent, selective and durable inhibition of the human protein methyltransferase DOT1L.Chem Biol Drug Des2012
21118801Genetic and pharmacological inhibition of PDK1 in cancer cells: characterization of a selective allosteric kinase inhibitor.J Biol Chem2011
21118801Genetic and pharmacological inhibition of PDK1 in cancer cells: characterization of a selective allosteric kinase inhibitor.J Biol Chem2011
21493594PDK1 attenuation fails to prevent tumor formation in PTEN-deficient transgenic mouse models.Cancer Res2011
21564555Chemogenetic analysis of human protein methyltransferases.Chem Biol Drug Des2011
21741597MLL-rearranged leukemia is dependent on aberrant H3K79 methylation by DOT1L.Cancer Cell2011
21741596Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L inhibitor.Cancer Cell2011
21856302The Y641C mutation of EZH2 alters substrate specificity for histone H3 lysine 27 methylation states.FEBS Lett2011
21856302The Y641C mutation of EZH2 alters substrate specificity for histone H3 lysine 27 methylation states.FEBS Lett2011
21564555Chemogenetic analysis of human protein methyltransferases.Chem Biol Drug Des2011
21741597MLL-rearranged leukemia is dependent on aberrant H3K79 methylation by DOT1L.Cancer Cell2011
21741596Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L inhibitor.Cancer Cell2011
21493594PDK1 attenuation fails to prevent tumor formation in PTEN-deficient transgenic mouse models.Cancer Res2011
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Co-authored papers 7
Goldfinch Bio Inc.
Co-authored papers 6
Memorial Sloan Kettering Cancer Center
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Boston Children's Hospital
Co-authored papers 4
Merck & Co., Inc.
Co-authored papers 3
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Co-authored papers 2
Peter MacCallum Cancer Centre
Co-authored papers 2
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Yale University School of Medicine
Co-authored papers 2
MD Anderson Cancer Center
Co-authored papers 2
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Co-authored papers 2
TESARO Inc.
Co-authored papers 2
Drug Metabolism and Pharmacokinetics
Co-authored papers 1
Center for Cancer Training, National Cancer Institute, National Institutes of Health
Co-authored papers 1
Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center
Co-authored papers 1
Program Resources Inc. NCI-FCDRC
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tranSMART Foundation
Co-authored papers 1
Center for Cancer Research, National Cancer Institute, National Institutes of Health
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Memorial Sloan Kettering Cancer Center
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Science Applications International Corporation/Frederick
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The University of Texas MD Anderson Cancer Center
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Georgia Cancer Center
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