Literature DB >> 31239270

EN1 Is a Transcriptional Dependency in Triple-Negative Breast Cancer Associated with Brain Metastasis.

Guillermo Peluffo1,2, Ashim Subedee1,3, Nicholas W Harper1, Natalie Kingston1, Bojana Jovanović1,2, Felipe Flores1,4, Laura E Stevens1,2, Francisco Beca5,6, Anne Trinh1,2, Chandra Sekhar Reddy Chilamakuri7, Evangelia K Papachristou7, Katherine Murphy1, Ying Su1,2, Andriy Marusyk1,2, Clive S D'Santos7, Oscar M Rueda7, Andrew H Beck5,6, Carlos Caldas7, Jason S Carroll7, Kornelia Polyak8,2,3.   

Abstract

To define transcriptional dependencies of triple-negative breast cancer (TNBC), we identified transcription factors highly and specifically expressed in primary TNBCs and tested their requirement for cell growth in a panel of breast cancer cell lines. We found that EN1 (engrailed 1) is overexpressed in TNBCs and its downregulation preferentially and significantly reduced viability and tumorigenicity in TNBC cell lines. By integrating gene expression changes after EN1 downregulation with EN1 chromatin binding patterns, we identified genes involved in WNT and Hedgehog signaling, neurogenesis, and axonal guidance as direct EN1 transcriptional targets. Quantitative proteomic analyses of EN1-bound chromatin complexes revealed association with transcriptional repressors and coactivators including TLE3, TRIM24, TRIM28, and TRIM33. High expression of EN1 correlated with short overall survival and increased risk of developing brain metastases in patients with TNBC. Thus, EN1 is a prognostic marker and a potential therapeutic target in TNBC. SIGNIFICANCE: These findings show that the EN1 transcription factor regulates neurogenesis-related genes and is associated with brain metastasis in triple-negative breast cancer. ©2019 American Association for Cancer Research.

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Year:  2019        PMID: 31239270      PMCID: PMC6698222          DOI: 10.1158/0008-5472.CAN-18-3264

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  36 in total

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2.  STRING: a web-server to retrieve and display the repeatedly occurring neighbourhood of a gene.

Authors:  B Snel; G Lehmann; P Bork; M A Huynen
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3.  Engrailed genes are cell-autonomously required to prevent apoptosis in mesencephalic dopaminergic neurons.

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Journal:  Development       Date:  2004-06-02       Impact factor: 6.868

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5.  Beta-catenin activation is necessary and sufficient to specify the dorsal dermal fate in the mouse.

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Journal:  Dev Biol       Date:  2006-04-21       Impact factor: 3.582

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Authors:  Tracey A Martin; Amit Goyal; Gareth Watkins; Wen G Jiang
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Authors:  Liora Bachar-Dahan; Janna Goltzmann; Abraham Yaniv; Arnona Gazit
Journal:  Mol Biol Cell       Date:  2006-03-29       Impact factor: 4.138

8.  Transcription cofactors TRIM24, TRIM28, and TRIM33 associate to form regulatory complexes that suppress murine hepatocellular carcinoma.

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Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-29       Impact factor: 11.205

9.  Combining Mixture Components for Clustering.

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  18 in total

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2.  Joint dimension reduction and clustering analysis of single-cell RNA-seq and spatial transcriptomics data.

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Review 3.  The roles of epigenetics in cancer progression and metastasis.

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5.  Identification of Key Differentially Expressed Transcription Factors in Glioblastoma.

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6.  Coupled Genome-Wide DNA Methylation and Transcription Analysis Identified Rich Biomarkers and Drug Targets in Triple-Negative Breast Cancer.

Authors:  Maoni Guo; Siddharth Sinha; San Ming Wang
Journal:  Cancers (Basel)       Date:  2019-11-04       Impact factor: 6.639

7.  Therapeutic and Mechanistic Perspectives of Protein Complexes in Breast Cancer.

Authors:  Mark P Waterhouse; Rosie Ugur; Walid T Khaled
Journal:  Front Cell Dev Biol       Date:  2019-12-20

8.  Identification of a Novel Transcription Factor Prognostic Index for Breast Cancer.

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Review 9.  "Triple-Negative Breast Cancer Central Nervous System Metastases From the Laboratory to the Clinic".

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10.  Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation.

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