TY - JOUR
T1 - Identification of four potential epigenetic modulators from the NCI structural diversity library using a cell-based assay
AU - Martinez, Elisabeth D.
AU - Best, Anne M.
AU - Chang, Jianjun
AU - Dull, Angie B.
AU - Beutler, John A.
PY - 2011
Y1 - 2011
N2 - Epigenetic pathways help control the expression of genes. In cancer and other diseases, aberrant silencing or overexpression of genes, such as those that control cell growth, can greatly contribute to pathogenesis. Access to these genes by the transcriptional machinery is largely mediated by chemical modifications of DNA or histones, which are controlled by epigenetic enzymes, making these enzymes attractive targets for drug discovery. Here we describe the characterization of a locus derepression assay, a fluorescence-based mammalian cellular system which was used to screen the NCI structural diversity library for novel epigenetic modulators using an automated imaging platform. Four structurally unique compounds were uncovered that, when further investigated, showed distinct activities. These compounds block the viability of lung cancer and melanoma cells, prevent cell cycle progression, and/or inhibit histone deacetylase activity, altering levels of cellular histone acetylation.
AB - Epigenetic pathways help control the expression of genes. In cancer and other diseases, aberrant silencing or overexpression of genes, such as those that control cell growth, can greatly contribute to pathogenesis. Access to these genes by the transcriptional machinery is largely mediated by chemical modifications of DNA or histones, which are controlled by epigenetic enzymes, making these enzymes attractive targets for drug discovery. Here we describe the characterization of a locus derepression assay, a fluorescence-based mammalian cellular system which was used to screen the NCI structural diversity library for novel epigenetic modulators using an automated imaging platform. Four structurally unique compounds were uncovered that, when further investigated, showed distinct activities. These compounds block the viability of lung cancer and melanoma cells, prevent cell cycle progression, and/or inhibit histone deacetylase activity, altering levels of cellular histone acetylation.
UR - http://www.scopus.com/inward/record.url?scp=79952234999&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79952234999&partnerID=8YFLogxK
U2 - 10.1155/2011/868095
DO - 10.1155/2011/868095
M3 - Article
C2 - 21234371
AN - SCOPUS:79952234999
SN - 2314-6133
VL - 2011
JO - BioMed Research International
JF - BioMed Research International
M1 - 868095
ER -