Response to Hydralazine-Valproate in a Patient with Mycosis Fungoides
Author(s) -
Alfonso DueñasGonzález,
María Teresa Vega Rodríguez,
Déborah Martı́nez-Baños,
Linda GarcíaHidalgo,
Pedro Sobrevilla
Publication year - 2010
Publication title -
case reports in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.2
H-Index - 20
eISSN - 1687-9627
pISSN - 1687-9635
DOI - 10.1155/2010/657579
Subject(s) - mycosis fungoides , medicine , histone deacetylase , hydralazine , cancer research , epigenetics , histone , dna methylation , demethylating agent , pharmacology , dermatology , dna , gene , biology , lymphoma , genetics , gene expression , blood pressure
Histone deacetylase (HDAC) inhibitors have shown significant activity in the treatment of cutaneous T-cell lymphomas (CTCL). The epigenetic alterations of CTCL not only are limited to altered histone acetylation but also include aberrant DNA gene methylation hence, the combination of an HDAC inhibitor with a DNA demethylating agent is a promising therapy to be tested. Here we report a mycosis fungoides patient having a dramatic response to hydralazine and valproate, two repositioned drugs as HDAC and DNA methylation inhibitors, respectively.
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