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Author Details
Full Name
Victoria M Richon
Affiliation
Discovery and Preclinical Sciences
ORCID
Career Start Year
1984
Papers
118
H Index
73
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34375612
PARP7 negatively regulates the type I interferon response in cancer cells and its inhibition triggers antitumor immunity.
Cancer Cell
2021
33705687
A potent and selective PARP14 inhibitor decreases protumor macrophage gene expression and elicits inflammatory responses in tumor explants.
Cell Chem Biol
2021
34375612
PARP7 negatively regulates the type I interferon response in cancer cells and its inhibition triggers antitumor immunity.
Cancer Cell
2021
33705687
A potent and selective PARP14 inhibitor decreases protumor macrophage gene expression and elicits inflammatory responses in tumor explants.
Cell Chem Biol
2021
28950000
Glutaminase 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 One
2017
28950000
Glutaminase 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 One
2017
26769278
The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat.
J Med Chem
2016
26769278
The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat.
J Med Chem
2016
25979925
CCR 20th Anniversary Commentary: Vorinostat-Gateway to Epigenetic Therapy.
Clin Cancer Res
2015
25897982
Redox-Mediated Suberoylanilide Hydroxamic Acid Sensitivity in Breast Cancer.
Antioxid Redox Signal
2015
26222556
Structural Approaches to Cancer Drug Development.
N Engl J Med
2015
25979925
CCR 20th Anniversary Commentary: Vorinostat-Gateway to Epigenetic Therapy.
Clin Cancer Res
2015
26222556
Structural Approaches to Cancer Drug Development.
N Engl J Med
2015
25897982
Redox-Mediated Suberoylanilide Hydroxamic Acid Sensitivity in Breast Cancer.
Antioxid Redox Signal
2015
24415392
Nonclinical pharmacokinetics and metabolism of EPZ-5676, a novel DOT1L histone methyltransferase inhibitor.
Biopharm Drug Dispos
2014
24415392
Nonclinical pharmacokinetics and metabolism of EPZ-5676, a novel DOT1L histone methyltransferase inhibitor.
Biopharm Drug Dispos
2014
24563539
Selective inhibition of EZH2 by EPZ-6438 leads to potent antitumor activity in EZH2-mutant non-Hodgkin lymphoma.
Mol Cancer Ther
2014
24563539
Selective inhibition of EZH2 by EPZ-6438 leads to potent antitumor activity in EZH2-mutant non-Hodgkin lymphoma.
Mol Cancer Ther
2014
23138183
Abrogation of MLL-AF10 and CALM-AF10-mediated transformation through genetic inactivation or pharmacological inhibition of the H3K79 methyltransferase Dot1l.
Leukemia
2013
23801631
Potent inhibition of DOT1L as treatment of MLL-fusion leukemia.
Blood
2013
24092806
Molecular and biologic analysis of histone deacetylase inhibitors with diverse specificities.
Mol Cancer Ther
2013
24319157
Drug discovery in rare indications: opportunities and challenges.
Hematology Am Soc Hematol Educ Program
2013
23361907
Leukemic transformation by the MLL-AF6 fusion oncogene requires the H3K79 methyltransferase Dot1l.
Blood
2013
23138183
Abrogation of MLL-AF10 and CALM-AF10-mediated transformation through genetic inactivation or pharmacological inhibition of the H3K79 methyltransferase Dot1l.
Leukemia
2013
23620515
Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2.
Proc Natl Acad Sci U S A
2013
23160372
Targeting genetic alterations in protein methyltransferases for personalized cancer therapeutics.
Oncogene
2013
24319157
Drug discovery in rare indications: opportunities and challenges.
Hematology Am Soc Hematol Educ Program
2013
24092806
Molecular and biologic analysis of histone deacetylase inhibitors with diverse specificities.
Mol Cancer Ther
2013
23620515
Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2.
Proc Natl Acad Sci U S A
2013
23801631
Potent inhibition of DOT1L as treatment of MLL-fusion leukemia.
Blood
2013
23160372
Targeting genetic alterations in protein methyltransferases for personalized cancer therapeutics.
Oncogene
2013
23361907
Leukemic transformation by the MLL-AF6 fusion oncogene requires the H3K79 methyltransferase Dot1l.
Blood
2013
22850114
A687V EZH2 is a gain-of-function mutation found in lymphoma patients.
FEBS Lett
2012
22850114
A687V EZH2 is a gain-of-function mutation found in lymphoma patients.
FEBS Lett
2012
22978415
Conformational adaptation drives potent, selective and durable inhibition of the human protein methyltransferase DOT1L.
Chem Biol Drug Des
2012
23023262
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.
Nat Chem Biol
2012
23023262
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.
Nat Chem Biol
2012
22978415
Conformational adaptation drives potent, selective and durable inhibition of the human protein methyltransferase DOT1L.
Chem Biol Drug Des
2012
21118801
Genetic and pharmacological inhibition of PDK1 in cancer cells: characterization of a selective allosteric kinase inhibitor.
J Biol Chem
2011
21118801
Genetic and pharmacological inhibition of PDK1 in cancer cells: characterization of a selective allosteric kinase inhibitor.
J Biol Chem
2011
21493594
PDK1 attenuation fails to prevent tumor formation in PTEN-deficient transgenic mouse models.
Cancer Res
2011
21564555
Chemogenetic analysis of human protein methyltransferases.
Chem Biol Drug Des
2011
21741597
MLL-rearranged leukemia is dependent on aberrant H3K79 methylation by DOT1L.
Cancer Cell
2011
21741596
Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L inhibitor.
Cancer Cell
2011
21856302
The Y641C mutation of EZH2 alters substrate specificity for histone H3 lysine 27 methylation states.
FEBS Lett
2011
21856302
The Y641C mutation of EZH2 alters substrate specificity for histone H3 lysine 27 methylation states.
FEBS Lett
2011
21564555
Chemogenetic analysis of human protein methyltransferases.
Chem Biol Drug Des
2011
21741597
MLL-rearranged leukemia is dependent on aberrant H3K79 methylation by DOT1L.
Cancer Cell
2011
21741596
Selective killing of mixed lineage leukemia cells by a potent small-molecule DOT1L inhibitor.
Cancer Cell
2011
21493594
PDK1 attenuation fails to prevent tumor formation in PTEN-deficient transgenic mouse models.
Cancer Res
2011
1 - 50 of 236
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