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Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210

The mode of antiproliferative action of deoxyspergualin (NKT‐01) was examined. The growth‐inhibitory effect on a murine leukemia cell line L1210 following treatment with NKT‐01 was time‐dependent, and there was little or no effect on the syntheses of DNA and RNA. Thus, the inhibitory activity of NKT...

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Autores principales: Hiratsuka, Masaharu, Kuramochi, Hiroshi, Takahashi, Katsutoshi, Takeuchi, Tomio, Mitsuo, Mitsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918251/
https://www.ncbi.nlm.nih.gov/pubmed/1955375
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01758.x
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author Hiratsuka, Masaharu
Kuramochi, Hiroshi
Takahashi, Katsutoshi
Takeuchi, Tomio
Mitsuo, Mitsuo
author_facet Hiratsuka, Masaharu
Kuramochi, Hiroshi
Takahashi, Katsutoshi
Takeuchi, Tomio
Mitsuo, Mitsuo
author_sort Hiratsuka, Masaharu
collection PubMed
description The mode of antiproliferative action of deoxyspergualin (NKT‐01) was examined. The growth‐inhibitory effect on a murine leukemia cell line L1210 following treatment with NKT‐01 was time‐dependent, and there was little or no effect on the syntheses of DNA and RNA. Thus, the inhibitory activity of NKT‐01 was not attributable to the inhibition of DNA and RNA syntheses. The influence of NKT‐01 on cell cycle progression was studied by flow cytometric analysis. Bromodeoxyuridine/DNA distribution patterns in cells that were treated for 72 h, showed that the growth inhibition is due to the delay of cell cycle progression but not to cytotoxicity. This finding was also supported by evidence that the treated cells were re‐proliferative in fresh medium. In addition, a majority of drug‐treated cells was prevented from traversing from the G(0)/G(1) phase to the S phase by 144 h or longer exposure to NKT‐01. The results suggest that NKT‐01 is cytostatic, preventing G(0)/G(1)‐S progression.
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spelling pubmed-59182512018-05-11 Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210 Hiratsuka, Masaharu Kuramochi, Hiroshi Takahashi, Katsutoshi Takeuchi, Tomio Mitsuo, Mitsuo Jpn J Cancer Res Article The mode of antiproliferative action of deoxyspergualin (NKT‐01) was examined. The growth‐inhibitory effect on a murine leukemia cell line L1210 following treatment with NKT‐01 was time‐dependent, and there was little or no effect on the syntheses of DNA and RNA. Thus, the inhibitory activity of NKT‐01 was not attributable to the inhibition of DNA and RNA syntheses. The influence of NKT‐01 on cell cycle progression was studied by flow cytometric analysis. Bromodeoxyuridine/DNA distribution patterns in cells that were treated for 72 h, showed that the growth inhibition is due to the delay of cell cycle progression but not to cytotoxicity. This finding was also supported by evidence that the treated cells were re‐proliferative in fresh medium. In addition, a majority of drug‐treated cells was prevented from traversing from the G(0)/G(1) phase to the S phase by 144 h or longer exposure to NKT‐01. The results suggest that NKT‐01 is cytostatic, preventing G(0)/G(1)‐S progression. Blackwell Publishing Ltd 1991-10 /pmc/articles/PMC5918251/ /pubmed/1955375 http://dx.doi.org/10.1111/j.1349-7006.1991.tb01758.x Text en
spellingShingle Article
Hiratsuka, Masaharu
Kuramochi, Hiroshi
Takahashi, Katsutoshi
Takeuchi, Tomio
Mitsuo, Mitsuo
Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title_full Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title_fullStr Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title_full_unstemmed Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title_short Cytostatic Effect of Deoxyspergualin on a Murine Leukemia Cell Line L1210
title_sort cytostatic effect of deoxyspergualin on a murine leukemia cell line l1210
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918251/
https://www.ncbi.nlm.nih.gov/pubmed/1955375
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01758.x
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