Show simple item record

dc.creatorMauer, Alvin M.en_US
dc.creatorLampkin, Beatrice C.en_US
dc.date.accessioned2006-07-06T20:41:40Z
dc.date.available2006-07-06T20:41:40Z
dc.date.issued1973-01en_US
dc.identifier.citationThe Ohio Journal of Science. v73, n1 (January, 1973), 11-15en_US
dc.identifier.issn0030-0950en_US
dc.identifier.urihttp://hdl.handle.net/1811/21949
dc.descriptionAuthor Institution: Department of Pediatrics, University of Cincinnati, and The Children's Hospital, and The Children's Hospital Research Foundationen_US
dc.description.abstractIn 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.extent467069 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.titleCellular Kinetics in Acute Leukemiaen_US


Files in this item

Thumbnail

Items in Knowledge Bank are protected by copyright, with all rights reserved, unless otherwise indicated.

This item appears in the following Collection(s)

Show simple item record