Literature DB >> 23210854

Histone methyltransferase inhibitors: novel epigenetic agents for cancer treatment.

C Zagni1, U Chiacchio, A Rescifina.   

Abstract

Epigenetics is defined as heritable changes in gene activity and expression that occur without alteration in DNA sequence. The gene transcription is strictly correlated to chromatin structure, which could undergo covalent modifications of histones involving acetylation, methylation, phosphorylation and ubiquitination. Alterations in histones are implicated in many diseases, including cancer, by leading to tumor suppressor silencing or pro-apoptotic proteins downregulation. Although post-translational addition of methyl groups to the histone lysine has been discovered three decades ago, the importance of this epigenetic modification has emerged only in the last few years. Thenceforward histone methyltransferase inhibitors have been developed as potential therapeutic cancer agents. It should not be long before some selective inhibitors make their way into clinical trials. This review is mainly focused on the evolution in the development of new epigenetic modifier molecules modulating histone marks.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23210854     DOI: 10.2174/092986713804806667

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  21 in total

Review 1.  Inhibitors of Protein Methyltransferases and Demethylases.

Authors:  H Ümit Kaniskan; Michael L Martini; Jian Jin
Journal:  Chem Rev       Date:  2017-03-24       Impact factor: 60.622

Review 2.  Recent progress in developing selective inhibitors of protein methyltransferases.

Authors:  H Ümit Kaniskan; Jian Jin
Journal:  Curr Opin Chem Biol       Date:  2017-06-26       Impact factor: 8.822

Review 3.  Lysine methyltransferase inhibitors: where we are now.

Authors:  Alessandra Feoli; Monica Viviano; Alessandra Cipriano; Ciro Milite; Sabrina Castellano; Gianluca Sbardella
Journal:  RSC Chem Biol       Date:  2021-12-13

4.  TNKS inhibitors potentiate proliferative inhibition of BET inhibitors via reducing β-Catenin in colorectal cancer cells.

Authors:  Qian Wu; Yi-Fei Xuan; Ai-Ling Su; Xu-Bin Bao; Ze-Hong Miao; Ying-Qing Wang
Journal:  Am J Cancer Res       Date:  2022-03-15       Impact factor: 6.166

Review 5.  PALB2: the hub of a network of tumor suppressors involved in DNA damage responses.

Authors:  Jung-Young Park; Fan Zhang; Paul R Andreassen
Journal:  Biochim Biophys Acta       Date:  2014-07-03

Review 6.  Epigenetic therapy in gastrointestinal cancer: the right combination.

Authors:  Eihab Abdelfatah; Zachary Kerner; Nainika Nanda; Nita Ahuja
Journal:  Therap Adv Gastroenterol       Date:  2016-05-01       Impact factor: 4.409

7.  Epigenetics in gastrointestinal stromal tumors: clinical implications and potential therapeutic perspectives.

Authors:  Athanasios D Sioulas; Diamantina Vasilatou; Vasiliki Pappa; George Dimitriadis; Konstantinos Triantafyllou
Journal:  Dig Dis Sci       Date:  2013-07-20       Impact factor: 3.199

8.  Histone modifications: implications in renal cell carcinoma.

Authors:  Swathi Ramakrishnan; Leigh Ellis; Roberto Pili
Journal:  Epigenomics       Date:  2013-08       Impact factor: 4.778

9.  Inhibition of the G9a/GLP histone methyltransferase complex modulates anxiety-related behavior in mice.

Authors:  Dong-Yao Wang; Joel Kosowan; James Samsom; Laura Leung; Kai-Lai Zhang; Ying-Xiang Li; Yan Xiong; Jian Jin; Arturas Petronis; Gabriel Oh; Albert H C Wong
Journal:  Acta Pharmacol Sin       Date:  2018-02-08       Impact factor: 6.150

Review 10.  Six Years (2012-2018) of Researches on Catalytic EZH2 Inhibitors: The Boom of the 2-Pyridone Compounds.

Authors:  Rossella Fioravanti; Giulia Stazi; Clemens Zwergel; Sergio Valente; Antonello Mai
Journal:  Chem Rec       Date:  2018-10-19       Impact factor: 6.771

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.