Cellular Kinetics in Acute Leukemia
dc.creator | Mauer, Alvin M. | en_US |
dc.creator | Lampkin, Beatrice C. | en_US |
dc.date.accessioned | 2006-07-06T20:41:40Z | |
dc.date.available | 2006-07-06T20:41:40Z | |
dc.date.issued | 1973-01 | en_US |
dc.identifier.citation | The Ohio Journal of Science. v73, n1 (January, 1973), 11-15 | en_US |
dc.identifier.issn | 0030-0950 | en_US |
dc.identifier.uri | http://hdl.handle.net/1811/21949 | |
dc.description | Author Institution: Department of Pediatrics, University of Cincinnati, and The Children's Hospital, and The Children's Hospital Research Foundation | en_US |
dc.description.abstract | In most patients with acute leukemia, the generation time of leukemic cells is about (10 hours, longer than for normal cells. Approximate times for the phases of the cell cycle are: DNA synthesis (S), 20 hours; mitosis (M), 2 hours; and the post-synthesis and postmitosis rest phases (G2 and Gi), 2 and 36 hours, respectively. A most important finding has been that a variable proportion of leukemic cells are out of cycle, that is, are in a resting or Go state. These resting cells are in equilibrium with the dividing cells, and some, as yet unknown, control mechanism for leukemic-cell growth controls the flow of cells from one compartment to the other. A critical feature of the resting cells is that they are relatively resistant to cycle-dependent chemotherapeutic agents. Much information has been obtained concerning the effects of drugs on the proliferative characteristics of leukemic cells. This information provides the basis for designing regimens with better timing of drug administration and advantageous use of combined chemotherapy. | en_US |
dc.format.extent | 467069 bytes | |
dc.format.mimetype | application/pdf | |
dc.language.iso | en_US | |
dc.title | Cellular Kinetics in Acute Leukemia | en_US |
Files in this item
Items in Knowledge Bank are protected by copyright, with all rights reserved, unless otherwise indicated.