Literature DB >> 17464242

DNA methyltransferase inhibitors for cancer therapy.

Bodo Brueckner1, Dirk Kuck, Frank Lyko.   

Abstract

Aberrant DNA methylation patterns, including hypermethylation of tumor suppressor genes, have been described in many human cancers. These epigenetic mutations can be reversed by DNA methyltransferase inhibitors, which provide novel opportunities for cancer therapy. Clinical concepts for epigenetic therapies are currently being developed by using azanucleosides for the treatment of leukemias and other tumors. These trials will greatly benefit from the inclusion of molecular markers for monitoring epigenetic changes in patients and for maximizing biologic responses. In addition, novel inhibitors need to be developed that result in a direct and specific inhibition of DNA methyltransferase activity. Several recent developments indicate that rational design of small molecule DNA methyltransferase inhibitors is feasible and that this approach can result in the establishment of novel drug candidates. The use of novel DNA methyltransferase inhibitors in clinical trials that allow monitoring of drug-induced DNA methylation changes should provide the foundation for improved epigenetic cancer therapies.

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Year:  2007        PMID: 17464242     DOI: 10.1097/PPO.0b013e31803c7245

Source DB:  PubMed          Journal:  Cancer J        ISSN: 1528-9117            Impact factor:   3.360


  31 in total

1.  Preclinical study of the DNA repair inhibitor Dbait in combination with chemotherapy in colorectal cancer.

Authors:  Flavien Devun; Guilhem Bousquet; Julian Biau; Aurélie Herbette; Christophe Roulin; Frédérique Berger; Jian-Sheng Sun; Sylvie Robine; Marie Dutreix
Journal:  J Gastroenterol       Date:  2011-11-09       Impact factor: 7.527

Review 2.  Advances in microRNAs: implications for gene therapists.

Authors:  Rebecca T Marquez; Anton P McCaffrey
Journal:  Hum Gene Ther       Date:  2008-01       Impact factor: 5.695

3.  [Epigenetic modifications in autoimmune diseases].

Authors:  A Ramming; J H W Distler; G Schett; S Gay; A Jüngel
Journal:  Z Rheumatol       Date:  2014-09       Impact factor: 1.372

Review 4.  Serine, glycine and one-carbon units: cancer metabolism in full circle.

Authors:  Jason W Locasale
Journal:  Nat Rev Cancer       Date:  2013-07-04       Impact factor: 60.716

5.  Epigenetic perturbations in the pathogenesis of mustard toxicity; hypothesis and preliminary results.

Authors:  Ahmet Korkmaz; Hakan Yaren; Z Ilker Kunak; Bulent Uysal; Bulent Kurt; Turgut Topal; Levent Kenar; Ergun Ucar; Sukru Oter
Journal:  Interdiscip Toxicol       Date:  2008-12

6.  A quantitative high-throughput screen identifies potential epigenetic modulators of gene expression.

Authors:  Ronald L Johnson; Wenwei Huang; Ajit Jadhav; Christopher P Austin; James Inglese; Elisabeth D Martinez
Journal:  Anal Biochem       Date:  2007-12-25       Impact factor: 3.365

7.  Hypermethylation of genes for diagnosis and risk stratification of prostate cancer.

Authors:  Donkena Krishna Vanaja; Mathias Ehrich; Dirk Van den Boom; John C Cheville; R Jeffrey Karnes; Donald J Tindall; Charles R Cantor; Charles Y F Young
Journal:  Cancer Invest       Date:  2009-06       Impact factor: 2.176

Review 8.  DNA polymerases as therapeutic targets.

Authors:  Anthony J Berdis
Journal:  Biochemistry       Date:  2008-07-19       Impact factor: 3.162

9.  Early epigenetic changes and DNA damage do not predict clinical response in an overlapping schedule of 5-azacytidine and entinostat in patients with myeloid malignancies.

Authors:  Tamer E Fandy; James G Herman; Patrick Kerns; Anchalee Jiemjit; Elizabeth A Sugar; Si-Ho Choi; Allen S Yang; Timothy Aucott; Tianna Dauses; Rosalie Odchimar-Reissig; Jonathan Licht; Melanie J McConnell; Chris Nasrallah; Marianne K H Kim; Weijia Zhang; Yezou Sun; Anthony Murgo; Igor Espinoza-Delgado; Katharine Oteiza; Ibitayo Owoeye; Lewis R Silverman; Steven D Gore; Hetty E Carraway
Journal:  Blood       Date:  2009-06-22       Impact factor: 22.113

10.  DNA methylation-mediated down-regulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta.

Authors:  Boris Novakovic; Nick C Wong; Mandy Sibson; Hong-Kiat Ng; Ruth Morley; Ursula Manuelpillai; Thomas Down; Vardhman K Rakyan; Stephan Beck; Stefan Hiendleder; Claire T Roberts; Jeffrey M Craig; Richard Saffery
Journal:  J Biol Chem       Date:  2010-01-13       Impact factor: 5.157

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