Abstract |
The histone deacetylase inhibitor trichostatin A ( TSA) has been previously shown to block cellular growth in G2 and induce apoptosis in human pancreatic cancer cell lines. In order to better understand this phenomenon, we have analyzed the gene expression profiles in PaCa44 cells after treatment with TSA using microarrays containing 22,283 probesets. TSA was found to cause both the induction and repression of a large number of genes, although the number whose expression was up-regulated was greater than the number of genes that were down-regulated. When a threshold value of 3 was used as a cutoff level, a total of 306 (3.4%) of the detectable genes had altered expression. When categorized according to cellular function, the differentially expressed genes were found to be involved in a wide variety of cellular processes, including cell proliferation, signaling, regulation of transcription, and apoptosis. Moreover, Sp1/ Sp3 transcription factor binding sites were significantly more abundant among TSA-induced genes. One prominent feature was the increased ratio between the levels of expression of pro-apoptotic (BIM) and anti-apoptotic (Bcl-XL and Bcl-W) genes. This result was confirmed in eight additional pancreatic cancer cell lines after treatment with TSA, suggesting that this event may be a strong determinant for the induction of apoptosis by TSA.
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Authors | Patrick S Moore, Stefano Barbi, Massimo Donadelli, Chiara Costanzo, Claudio Bassi, Marta Palmieri, Aldo Scarpa |
Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 1693
Issue 3
Pg. 167-76
(Sep 17 2004)
ISSN: 0006-3002 [Print] Netherlands |
PMID | 15363630
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Enzyme Inhibitors
- Histone Deacetylase Inhibitors
- Hydroxamic Acids
- trichostatin A
- Histone Deacetylases
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Topics |
- Adenocarcinoma
(genetics)
- Apoptosis
(genetics)
- Enzyme Inhibitors
(pharmacology)
- Gene Expression Profiling
- Histone Deacetylase Inhibitors
- Histone Deacetylases
(physiology)
- Humans
- Hydroxamic Acids
(pharmacology)
- Pancreatic Neoplasms
(genetics)
- Reverse Transcriptase Polymerase Chain Reaction
- Tumor Cells, Cultured
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