Abstract |
Blast cells from patients with acute myeloblastic leukemia were exposed to 5-azacytidine (5-aza) and its analogues 5-aza 2'-deoxycytidine (5-aza-dr) and 6-azacytidine (6-aza). Simple negative exponential survival curves were obtained for the three drugs, but the sensitivity varied; 5-aza-dr was most toxic, 6-aza was least toxic, and 5-aza was intermediate. Colonies surviving drug exposure were replated; 5-aza and 5-aza-dr were found to increase secondary plating efficiency, whereas 6-aza was inactive. The findings provide indirect evidence for a role for DNA methylation in the regulation of blast cell self-renewal.
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Authors | T Motoji, T Hoang, D Tritchler, E A McCulloch |
Journal | Blood
(Blood)
Vol. 65
Issue 4
Pg. 894-901
(Apr 1985)
ISSN: 0006-4971 [Print] United States |
PMID | 2579689
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Culture Media
- Decitabine
- Azacitidine
- 6-azacytidine
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Topics |
- Azacitidine
(analogs & derivatives, pharmacology)
- Cell Division
(drug effects)
- Culture Media
- Decitabine
- Dose-Response Relationship, Drug
- Humans
- Leukemia, Myeloid, Acute
(blood, pathology)
- Neoplastic Stem Cells
(drug effects)
- Phenotype
- Stem Cells
(drug effects)
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