Research on cancer epigenetics has flourished in the last decade as growing evidence pointed on the importance to understand the mechanisms by which epigenetic changes regulate the genesis and progression of several pathologies, especially cancer. Several epigenetic targets have been discovered and are currently under validation for different therapies. In this context, drug discovery approaches aiming at developing new small-molecules modulators have produced the first pre-clinical and clinical outcomes and many other compounds are now entering the pipeline as new epidrugs. While most of the efforts have been dedicated in the past to histone deacetylases and DNA methyltransferases, other classes of enzymes are also likely to represent new frontiers for therapeutic interventions. In this chapter we describe the increasing importance of histone methyltransferases in the drug discovery arena and discuss the drug design perspectives enabled by computational techniques to develop new small-molecules inhibitors for these classes of enzymes.
Molecular Design of Compounds Targeting Histone Methyltransferases
Rio;Alberto Del;Varchi;Greta
2016
Abstract
Research on cancer epigenetics has flourished in the last decade as growing evidence pointed on the importance to understand the mechanisms by which epigenetic changes regulate the genesis and progression of several pathologies, especially cancer. Several epigenetic targets have been discovered and are currently under validation for different therapies. In this context, drug discovery approaches aiming at developing new small-molecules modulators have produced the first pre-clinical and clinical outcomes and many other compounds are now entering the pipeline as new epidrugs. While most of the efforts have been dedicated in the past to histone deacetylases and DNA methyltransferases, other classes of enzymes are also likely to represent new frontiers for therapeutic interventions. In this chapter we describe the increasing importance of histone methyltransferases in the drug discovery arena and discuss the drug design perspectives enabled by computational techniques to develop new small-molecules inhibitors for these classes of enzymes.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.