Literature DB >> 28071961

Cellular analysis of the action of epigenetic drugs and probes.

Mirjam Hau1, Fides Zenk2, A Ganesan3,4, Nicola Iovino2, Manfred Jung1,4.   

Abstract

Small molecule drugs and probes are important tools in drug discovery, pharmacology, and cell biology. This is of course also true for epigenetic inhibitors. Important examples for the use of established epigenetic inhibitors are the study of the mechanistic role of a certain target in a cellular setting or the modulation of a certain phenotype in an approach that aims toward therapeutic application. Alternatively, cellular testing may aim at the validation of a new epigenetic inhibitor in drug discovery approaches. Cellular and eventually animal models provide powerful tools for these different approaches but certain caveats have to be recognized and taken into account. This involves both the selectivity of the pharmacological tool as well as the specificity and the robustness of the cellular system. In this article, we present an overview of different methods that are used to profile and screen for epigenetic agents and comment on their limitations. We describe not only diverse successful case studies of screening approaches using different assay formats, but also some problematic cases, critically discussing selected applications of these systems.

Keywords:  Chem-seq; Chip-seq; Epigenetics; cellular models; chemical probes; epigenetic drugs; screening

Mesh:

Substances:

Year:  2017        PMID: 28071961      PMCID: PMC5453192          DOI: 10.1080/15592294.2016.1274472

Source DB:  PubMed          Journal:  Epigenetics        ISSN: 1559-2294            Impact factor:   4.528


  105 in total

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Authors:  Alexander-Thomas Hauser; Julia M Gajer Née Wagner; Manfred Jung
Journal:  Methods Mol Biol       Date:  2013

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Authors:  Rozbeh Jafari; Helena Almqvist; Hanna Axelsson; Marina Ignatushchenko; Thomas Lundbäck; Pär Nordlund; Daniel Martinez Molina
Journal:  Nat Protoc       Date:  2014-08-07       Impact factor: 13.491

6.  The histone demethylase LSD1 is required for estrogen-dependent S100A7 gene expression in human breast cancer cells.

Authors:  Seung Eun Yu; Yeun Kyu Jang
Journal:  Biochem Biophys Res Commun       Date:  2012-09-18       Impact factor: 3.575

7.  Chrysin: a histone deacetylase 8 inhibitor with anticancer activity and a suitable candidate for the standardization of Chinese propolis.

Authors:  Li-Ping Sun; Ai-Ling Chen; Hsiao-Chiao Hung; Yin-Huan Chien; Jing-Shi Huang; Chung-Yang Huang; Yue-Wen Chen; Chia-Nan Chen
Journal:  J Agric Food Chem       Date:  2012-11-15       Impact factor: 5.279

8.  Plant HDAC inhibitor chrysin arrest cell growth and induce p21WAF1 by altering chromatin of STAT response element in A375 cells.

Authors:  Manika Pal-Bhadra; M Janaki Ramaiah; T Lakshminarayan Reddy; Anita Krishnan; S N C V L Pushpavalli; K Suresh Babu; Ashok K Tiwari; J Madhusudana Rao; Jhillu S Yadav; Utpal Bhadra
Journal:  BMC Cancer       Date:  2012-05-16       Impact factor: 4.430

9.  The histone code reader SPIN1 controls RET signaling in liposarcoma.

Authors:  Henriette Franz; Holger Greschik; Dominica Willmann; Luka Ozretić; Cordula Annette Jilg; Eva Wardelmann; Manfred Jung; Reinhard Buettner; Roland Schüle
Journal:  Oncotarget       Date:  2015-03-10

10.  A Rational Approach for the Identification of Non-Hydroxamate HDAC6-Selective Inhibitors.

Authors:  Laura Goracci; Nathalie Deschamps; Giuseppe Marco Randazzo; Charlotte Petit; Carolina Dos Santos Passos; Pierre-Alain Carrupt; Claudia Simões-Pires; Alessandra Nurisso
Journal:  Sci Rep       Date:  2016-07-12       Impact factor: 4.379

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  1 in total

1.  Epigenetic drugs: More than meets the eye.

Authors:  Manel Esteller
Journal:  Epigenetics       Date:  2017-05-04       Impact factor: 4.528

  1 in total

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