Effect of phenylbutyrate, a histone deacetylase inhibitor, on differentiation and apoptosis of Kasumi-1 cells / 中华血液学杂志
Chinese Journal of Hematology
;
(12): 241-244, 2003.
Article
in Chinese
| WPRIM
| ID: wpr-354880
ABSTRACT
<p><b>OBJECTIVE</b>To explore the blockade effect of phenylbutyrate (PB), a histone deacetylase inhibitor, on the in vitro biological function of AML1/ETO to reverse its transcription repression and induce Kasumi-1 cells to differentiate and apoptosis.</p><p><b>METHODS</b>Kasumi-1 cells were treated with PB at different concentrations in suspension culture. Cell proliferation was analysed by MTT assay, morphological changes by light and electron microscopy, expression of myeloid-specific differentiation antigen and cell cycle by flow cytometry, cell apoptosis by annexin V staining, agarose gel electrophoresis and flow cytometry.</p><p><b>RESULTS</b>PB treatment caused a dose-dependent inhibition of the cell proliferation. The IC(50) was about 2.3 mmol/L. PB treatment led to a progressive decline in the fraction of S-phase cells and increase in G(0)/G(1) cells. PB induced a time- and dose-dependent increase in expression of myeloid cell surface protein CD(11b) and CD(13). A dose-dependent increase in early apoptosis for 2 days treatment, late apoptosis for 3 days treatment. The DNA ladder of apoptosis was observed on agarose gel electrophoresis for 5 days treatment. Morphological features of monocytoid differentiation and apoptosis were seen on Wright-Giemsa staining smears.</p><p><b>CONCLUSION</b>PB treatment could inhibit proliferation of Kasumi-1 cells, induce partial differentiation, apoptosis and accumulation of cells in G(0)/G(1) phase.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pathology
/
Pharmacology
/
Phenylbutyrates
/
Leukemia, Myeloid, Acute
/
Cell Differentiation
/
Cell Division
/
Apoptosis
/
Cell Line, Tumor
/
Dose-Response Relationship, Drug
/
Histone Deacetylase Inhibitors
Limits:
Humans
Language:
Chinese
Journal:
Chinese Journal of Hematology
Year:
2003
Type:
Article
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