Literature DB >> 25468267

KDM4 histone demethylase inhibitors for anti-cancer agents: a patent review.

Young-Won Chin1, Sun-Young Han.   

Abstract

INTRODUCTION: As epigenetic modulators, histone demethylases can be a therapeutic target in the area of oncology. KDM4 subfamily proteins are histone demethylases with a Jumonji domain. The subfamily consists of five functional members: KDM4A, KDM4B, KDM4C, KDM4D, and KDM4E. The role of the KDM4 subfamily proteins is reported in oncogenesis, and their overexpression in various tumor types is observed. Small molecule inhibitors for KDM4 proteins have great potential in anti-cancer therapy. AREAS COVERED: A comprehensive review of the patents for KDM4 inhibitors is provided in this paper. Small molecule structural information and pharmacological effects are presented in the content. EXPERT OPINION: The status of KDM4 inhibitor development is still in the early stages with small numbers of patents and journal articles. Future KDM4 inhibitor development should focus on obtaining selectivity between KDM4 subtypes, development of small molecules with in vivo activity, and extension of the therapeutic area of KDM4 inhibitors other than use in cancer therapy.

Entities:  

Keywords:  JHDM3; Jumonji D2; KDM4; epigenetics; histone demethylase

Mesh:

Substances:

Year:  2014        PMID: 25468267     DOI: 10.1517/13543776.2014.991310

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  14 in total

1.  Genome-wide Kdm4 histone demethylase transcriptional regulation in Drosophila.

Authors:  Amy Tsurumi; Shuang Xue; Lin Zhang; Jinghong Li; Willis X Li
Journal:  Mol Genet Genomics       Date:  2019-04-24       Impact factor: 3.291

Review 2.  Marked for death: targeting epigenetic changes in cancer.

Authors:  Sophia Xiao Pfister; Alan Ashworth
Journal:  Nat Rev Drug Discov       Date:  2017-03-10       Impact factor: 84.694

3.  Interaction of huntingtin with PRMTs and its subsequent arginine methylation affects HTT solubility, phase transition behavior and neuronal toxicity.

Authors:  Tamara Ratovitski; Mali Jiang; Robert N O'Meally; Priyanka Rauniyar; Ekaterine Chighladze; Anikó Faragó; Siddhi V Kamath; Jing Jin; Alexey V Shevelkin; Robert N Cole; Christopher A Ross
Journal:  Hum Mol Genet       Date:  2022-05-19       Impact factor: 5.121

4.  Novel inhibitors of lysine (K)-specific Demethylase 4A with anticancer activity.

Authors:  Hyo Jeong Lee; Bo-Kyoung Kim; Kyoung Bin Yoon; Yong-Chul Kim; Sun-Young Han
Journal:  Invest New Drugs       Date:  2017-09-14       Impact factor: 3.850

Review 5.  Epigenetic reprogramming during prostate cancer progression: A perspective from development.

Authors:  Sakshi Goel; Vipul Bhatia; Tanay Biswas; Bushra Ateeq
Journal:  Semin Cancer Biol       Date:  2021-02-02       Impact factor: 17.012

6.  The JmjN domain as a dimerization interface and a targeted inhibitor of KDM4 demethylase activity.

Authors:  May Levin; Michal Stark; Yehuda G Assaraf
Journal:  Oncotarget       Date:  2018-03-30

7.  Small molecule KDM4s inhibitors as anti-cancer agents.

Authors:  Hongzhi Lin; Qihang Li; Qi Li; Jie Zhu; Kai Gu; Xueyang Jiang; Qianqian Hu; Feng Feng; Wei Qu; Yao Chen; Haopeng Sun
Journal:  J Enzyme Inhib Med Chem       Date:  2018-12       Impact factor: 5.051

Review 8.  The Emerging Role of H3K9me3 as a Potential Therapeutic Target in Acute Myeloid Leukemia.

Authors:  Laura Monaghan; Matthew E Massett; Roderick P Bunschoten; Alex Hoose; Petrisor-Alin Pirvan; Robert M J Liskamp; Heather G Jørgensen; Xu Huang
Journal:  Front Oncol       Date:  2019-08-02       Impact factor: 6.244

9.  Histone lysine demethylase KDM4B regulates the alternative splicing of the androgen receptor in response to androgen deprivation.

Authors:  Lingling Duan; Zhenhua Chen; Jun Lu; Yanping Liang; Ming Wang; Carlos M Roggero; Qing-Jun Zhang; Jason Gao; Yong Fang; Jiazheng Cao; Jian Lu; Hongwei Zhao; Andrew Dang; Rey-Chen Pong; Elizabeth Hernandez; Chun-Mien Chang; David T Hoang; Jung-Mo Ahn; Guanghua Xiao; Rui-Tao Wang; Kai-Jiang Yu; Payal Kapur; Josep Rizo; Jer-Tsong Hsieh; Junhang Luo; Zhi-Ping Liu
Journal:  Nucleic Acids Res       Date:  2019-12-16       Impact factor: 19.160

10.  8-Substituted Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors.

Authors:  Vassilios Bavetsias; Rachel M Lanigan; Gian Filippo Ruda; Butrus Atrash; Mark G McLaughlin; Anthony Tumber; N Yi Mok; Yann-Vaï Le Bihan; Sally Dempster; Katherine J Boxall; Fiona Jeganathan; Stephanie B Hatch; Pavel Savitsky; Srikannathasan Velupillai; Tobias Krojer; Katherine S England; Jimmy Sejberg; Ching Thai; Adam Donovan; Akos Pal; Giuseppe Scozzafava; James M Bennett; Akane Kawamura; Catrine Johansson; Aleksandra Szykowska; Carina Gileadi; Nicola A Burgess-Brown; Frank von Delft; Udo Oppermann; Zoe Walters; Janet Shipley; Florence I Raynaud; Susan M Westaway; Rab K Prinjha; Oleg Fedorov; Rosemary Burke; Christopher J Schofield; Isaac M Westwood; Chas Bountra; Susanne Müller; Rob L M van Montfort; Paul E Brennan; Julian Blagg
Journal:  J Med Chem       Date:  2016-01-07       Impact factor: 7.446

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