Tri-methylation of H3K79 is decreased in TGF-β1-induced epithelial-to-mesenchymal transition in lung cancer

EMT: 2016

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DOT1L cooperates with the c-Myc-p300 complex to epigenetically derepress CDH1 transcription factors in breast cancer progression

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Regulation of mTOR Signaling by Semaphorin 3F-Neuropilin 2 Interactions In Vitro and In Vivo

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RE-IIBP Methylates H3K79 and Induces MEIS1-mediated Apoptosis via H2BK120 Ubiquitination by RNF20

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Neuropilin-2 Is Upregulated in Lung Cancer Cells during TGF- 1-Induced Epithelial-Mesenchymal Transition

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A Synthetic Lethality-Based Strategy to Treat Cancers Harboring a Genetic Deficiency in the Chromatin Remodeling Factor BRG1

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EZH2 Protein Expression Associates with the Early Pathogenesis, Tumor Progression, and Prognosis of Non-Small Cell Lung Carcinoma

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(2013) Vamsidhar Velcheti et al.   LABORATORY INVESTIGATION

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Epigenetic coordination of signaling pathways during the epithelial-mesenchymal transition

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Global Decrease of Histone H3K27 Acetylation in ZEB1-Induced Epithelial to Mesenchymal Transition in Lung Cancer Cells

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Lung cancer with loss of BRG1/BRM, shows epithelial mesenchymal transition phenotype and distinct histologic and genetic features

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Tumor B7-H1 and B7-H3 Expression in Squamous Cell Carcinoma of the Lung

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(2012) Steven A. Johnsen   FEBS LETTERS

Comprehensive genomic characterization of squamous cell lung cancers

(2012)   NATURE

Epigenetic protein families: a new frontier for drug discovery

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Lung cancer

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DOT1L/KMT4 Recruitment and H3K79 Methylation Are Ubiquitously Coupled with Gene Transcription in Mammalian Cells

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Nonprocessive methylation by Dot1 leads to functional redundancy of histone H3K79 methylation states

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