Title : Histone deacetylase inhibitor trichostatin a potentiates doxorubicin-induced apoptosis by up-regulating PTEN expression.

Pub. Date : 2007 Apr 15

PMID : 17330857






6 Functional Relationships(s)
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1 Histone deacetylase inhibitor trichostatin a potentiates doxorubicin-induced apoptosis by up-regulating PTEN expression. Doxorubicin phosphatase and tensin homolog Homo sapiens
2 Overexpression of PTEN by adenoviral transfection increases doxorubicin-induced apoptosis. Doxorubicin phosphatase and tensin homolog Homo sapiens
3 The aim of this work was to investigate whether changes in PTEN expression are involved in TSA/doxorubicin-induced apoptosis. Doxorubicin phosphatase and tensin homolog Homo sapiens
4 RESULTS: Doxorubicin-induced apoptosis was enhanced by TSA, whereas small interfering RNA (siRNA) targeting PTEN inhibited TSA/doxorubicin-induced apoptosis. Doxorubicin phosphatase and tensin homolog Homo sapiens
5 CONCLUSIONS: TSA promoted doxorubicin-induced apoptosis through a mechanism that involved the stimulation of Egr-1 expression, acetylation of core histones at the PTEN promoter, and consequently induction of PTEN transcription. Doxorubicin phosphatase and tensin homolog Homo sapiens
6 CONCLUSIONS: TSA promoted doxorubicin-induced apoptosis through a mechanism that involved the stimulation of Egr-1 expression, acetylation of core histones at the PTEN promoter, and consequently induction of PTEN transcription. Doxorubicin phosphatase and tensin homolog Homo sapiens