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Sunday November 22 2009 | Biotechnology feed | All feeds
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Chromatin methylation: An approach to gene silencing The drive to develop improved treatments of cancer has resulted in the birth of a number of highly exciting therapeutic field, apoptosis and angiogenesis offering just two recent examples. The field of histone deacetylation represents one of the most recent therapeutic targets to fall under the oncology spotlight. This field centers on the now generally accepted view that chromatin structure is plastic and that histone (de)acetylation regulates genome structure and hence transcription. Modifying this process by histone deacetylase (HDAC) inhibitors can therefore regulate, potentially in a highly specific manner, transcription thereby offering a much more targeted approach to cytostasis than currently available. Information relating to histone deacetylation is emerging with breathtaking rapidity with over 1 new article currently being published every day. In response to this activity we recently published one of the most comprehensive overview of the pharmaceutical potential of HDAC inhibitors to date ("Histone deacetylase inhibitors: Redefining pharmaceutical approaches to the treatment of cancer"). In this edition of TherapeuticAdvances we introduce another approach to modifying chromatin structure, methylation. Aberrant methylation patterns have been reported in an increasing number of tumor suppressor and DNA repair genes determining carcinogenetic transformation. On the other hand, methyl-DNA binding recruits co-repressor complexes and modifies the structure of the chromatin to produce a transcriptionally silenced state. Although this field has seen rapid progress in recent years, detailed mechanisms by which this machinery modifies chromatin structure to its appropriate state and the specific targeting of repressor complexes have yet to be resolved. Clicking the link below will take you a recent article describing some of the more recent developments in this area.
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