n-Butyric acid and its "polymorphic" derivatives have been largely but some
how "blindly" studied in oncology and in red cell diseases with consistent
results through decades indicating a strong maturative effect determined by
enhancement of gene transcription. Although these effects have been observ
ed mainly in vitro, the relative absence of systemic toxicity of butyrates
render these compounds appealing as specific therapeutic agents. More inter
estingly, their specific mechanism of action, i.e. inhibition of histone de
acetylase and de-repression of transcription represents at present an uniqu
e tool for diseases such as acute leukemias which are characterised by a di
sregulation of co-repressors and co-activators of gene transcription. More
insight into specificity and modalities of action of different butyrate der
ivatives may be a guarantee for excellent tailored antileukemic therapy in
the future.