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Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells
Author(s) -
Primeau Mélanie,
Gag Jacynthe,
Momparler Richard L.
Publication year - 2002
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.10789
Subject(s) - depsipeptide , histone deacetylase inhibitor , cancer research , histone deacetylase , deoxycytidine , chemistry , cancer , biology , histone , medicine , gemcitabine , dna , biochemistry
Abstract During tumorigenesis, cancer‐related genes can be silenced by aberrant DNA methylation and by changes in chromatin structure. It has been reported that 5‐aza‐2′‐deoxycytidine, a potent inhibitor of DNA methylation, in combination with histone deacetylase inhibitors, can produce a synergistic reactivation of these genes. The aim of our study was to investigate the in vitro antineoplastic activity of 5‐aza‐2′‐deoxycytidine in combination with depsipeptide, a potent histone deacetylase inhibitor, against MDA‐MB‐231 and MDA‐MB‐435 human breast carcinoma cell lines. We observed that the combination of 5‐aza‐2′‐deoxycytidine and depsipeptide produced a synergistic antineoplastic effect against these tumor cells as compared to either agent administered alone. We also investigated the effect of this drug combination on the activation of maspin and gelsolin expression. These 2 genes whose function is to suppress tumor metastasis have been reported to be silenced by epigenetic events in breast cancer. Using semi‐quantitative RT‐PCR, we observed that 5‐aza‐2′‐deoxycytidine in combination with depsipeptide produced a greater reactivation of both maspin and gelsolin as compared to each agent alone. The synergistic interaction between 5‐aza‐2′‐deoxycytidine and depsipeptide on breast carcinoma cell lines provides a rationale to investigate this interesting drug combination in future clinical trials on patients with advanced breast cancer. © 2002 Wiley‐Liss, Inc.