Open AccessAnticancer drug mithramycin interacts with core histones: An additional mode of action of the DNA groove binder
Author(s) -
Banerjee Amrita,
Sanyal Sulagna,
Kulkarni Kirti K.,
Jana Kuladip,
Roy Siddhartha,
Das Chandrima,
Dasgupta Dipak
Publication year - 2014
Publication title -
febs open bio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.718
H-Index - 31
ISSN - 2211-5463
DOI - 10.1016/j.fob.2014.10.007
Subject(s) - histone , chromatin , dna , histone modifying enzymes , biology , transcription factor , acetylation , chromatin immunoprecipitation , nucleosome , mode of action , microbiology and biotechnology , promoter , gene , genetics , chemistry , biochemistry , gene expression
Mithramycin (MTR) is a clinically approved DNA‐binding antitumor antibiotic currently in Phase 2 clinical trials at National Institutes of Health for treatment of osteosarcoma. In view of the resurgence in the studies of this generic antibiotic as a human medicine, we have examined the binding properties of MTR with the integral component of chromatin – histone proteins – as a part of our broad objective to classify DNA‐binding molecules in terms of their ability to bind chromosomal DNA alone (single binding mode) or both histones and chromosomal DNA (dual binding mode). The present report shows that besides DNA, MTR also binds to core histones present in chromatin and thus possesses the property of dual binding in the chromatin context. In contrast to the MTR–DNA interaction, association of MTR with histones does not require obligatory presence of bivalent metal ion like Mg 2+ . As a consequence of its ability to interact with core histones, MTR inhibits histone H3 acetylation at lysine 18, an important signature of active chromatin, in vitro and ex vivo . Reanalysis of microarray data of Ewing sarcoma cell lines shows that upon MTR treatment there is a significant down regulation of genes, possibly implicating a repression of H3K18Ac‐enriched genes apart from DNA‐binding transcription factors. Association of MTR with core histones and its ability to alter post‐translational modification of histone H3 clearly indicates an additional mode of action of this anticancer drug that could be implicated in novel therapeutic strategies.