Literature DB >> 30482069

Proteomic approaches for cancer epigenetics research.

Dylan M Marchione1, Benjamin A Garcia1, John Wojcik2.   

Abstract

Introduction: Epigenetic dysregulation drives or supports numerous human cancers. The chromatin landscape in cancer cells is often marked by abnormal histone post-translational modification (PTM) patterns and by aberrant assembly and recruitment of protein complexes to specific genomic loci. Mass spectrometry-based proteomic analyses can support the discovery and characterization of both phenomena. Areas covered: We broadly divide this literature into two parts: 'modification-centric' analyses that link histone PTMs to cancer biology; and 'complex-centric' analyses that examine protein-protein interactions that occur de novo as a result of oncogenic mutations. We also discuss proteomic studies of oncohistones. We highlight relevant examples, discuss limitations, and speculate about forthcoming innovations regarding each application. Expert commentary: 'Modification-centric' analyses have been used to further understanding of cancer's histone code and to identify associated therapeutic vulnerabilities. 'Complex-centric' analyses have likewise revealed insights into mechanisms of oncogenesis and suggested potential therapeutic targets, particularly in MLL-associated leukemia. Proteomic experiments have also supported some of the pioneering studies of oncohistone-mediated tumorigenesis. Additional applications of proteomics that may benefit cancer epigenetics research include middle-down and top-down histone PTM analysis, chromatin reader profiling, and genomic locus-specific protein identification. In the coming years, proteomic approaches will remain powerful ways to interrogate the biology of cancer.

Entities:  

Keywords:  Affinity proteomics; cancer; chromatin; epigenetics; histones; middle-down; readers; top-down

Mesh:

Substances:

Year:  2018        PMID: 30482069      PMCID: PMC6536358          DOI: 10.1080/14789450.2019.1550363

Source DB:  PubMed          Journal:  Expert Rev Proteomics        ISSN: 1478-9450            Impact factor:   3.940


  141 in total

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Journal:  Mol Cell       Date:  2002-11       Impact factor: 17.970

4.  Abnormal properties of histones from malignant cells.

Authors:  H J CRUFT; C M MAURITZEN; E STEDMAN
Journal:  Nature       Date:  1954-09-25       Impact factor: 49.962

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6.  MLL targets SET domain methyltransferase activity to Hox gene promoters.

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Journal:  Mol Cell       Date:  2002-11       Impact factor: 17.970

Review 7.  Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins.

Authors:  P M Ayton; M L Cleary
Journal:  Oncogene       Date:  2001-09-10       Impact factor: 9.867

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Authors:  Bernhard Lehnertz; Yoshihide Ueda; Alwin A H A Derijck; Ulrich Braunschweig; Laura Perez-Burgos; Stefan Kubicek; Taiping Chen; En Li; Thomas Jenuwein; Antoine H F M Peters
Journal:  Curr Biol       Date:  2003-07-15       Impact factor: 10.834

9.  BRD4-NUT fusion oncogene: a novel mechanism in aggressive carcinoma.

Authors:  Christopher A French; Isao Miyoshi; Ichiro Kubonishi; Holcombe E Grier; Antonio R Perez-Atayde; Jonathan A Fletcher
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  3 in total

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Journal:  J Am Soc Mass Spectrom       Date:  2019-09-11       Impact factor: 3.109

2.  Collision Cross Sections for Native Proteomics: Challenges and Opportunities.

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3.  Analysis of histone variant constraint and tissue expression suggests five potential novel human disease genes: H2AFY2, H2AFZ, H2AFY, H2AFV, H1F0.

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Journal:  Hum Genet       Date:  2022-01-24       Impact factor: 5.881

  3 in total

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