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Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700

Nine daily intravenous (iv) injections of RA‐700 (an antitumor cyclic hexapeptide) at doses of 2 to 6 mgAg/day caused increases of WBC counts at 4–6 days after treatment in normal C57BL/6 × DBA/ 2 (BDF1) mice. The percentages of neutrophils and lymphocytes were modified. There was a decrease of colo...

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Autores principales: Kato, Taketoshi, Suzumura, Yasuko, Liu, Fen‐Zhi, Tateno, Hiroo, Ogiu, Toshiaki, Ota, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917711/
https://www.ncbi.nlm.nih.gov/pubmed/2498262
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02307.x
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author Kato, Taketoshi
Suzumura, Yasuko
Liu, Fen‐Zhi
Tateno, Hiroo
Ogiu, Toshiaki
Ota, Kazuo
author_facet Kato, Taketoshi
Suzumura, Yasuko
Liu, Fen‐Zhi
Tateno, Hiroo
Ogiu, Toshiaki
Ota, Kazuo
author_sort Kato, Taketoshi
collection PubMed
description Nine daily intravenous (iv) injections of RA‐700 (an antitumor cyclic hexapeptide) at doses of 2 to 6 mgAg/day caused increases of WBC counts at 4–6 days after treatment in normal C57BL/6 × DBA/ 2 (BDF1) mice. The percentages of neutrophils and lymphocytes were modified. There was a decrease of colony‐forming units in culture (CFUc) in bone marrow to 40% of the control value on day 1 but CFUc rapidly returned to normal values on day 3. The colony‐forming units in spleen (CFUs): in bone marrow decreased during treatment. On the other hand, CFUc and CFUs in spleen were increased from the initiation of treatment to the time prior to the increase of WBC count. Spleen weight increased after treatment, and histologically, increases of immature and also mature granulocytes and megakaryocytes were observed. However, RA‐700 did not stimulate the progress of hematoprogenitors in vitro. The results indicated that RA‐700 stimulates the progress of hematoprogenitors in the spleen, but this effect is probably indirect.
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spelling pubmed-59177112018-05-11 Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700 Kato, Taketoshi Suzumura, Yasuko Liu, Fen‐Zhi Tateno, Hiroo Ogiu, Toshiaki Ota, Kazuo Jpn J Cancer Res Article Nine daily intravenous (iv) injections of RA‐700 (an antitumor cyclic hexapeptide) at doses of 2 to 6 mgAg/day caused increases of WBC counts at 4–6 days after treatment in normal C57BL/6 × DBA/ 2 (BDF1) mice. The percentages of neutrophils and lymphocytes were modified. There was a decrease of colony‐forming units in culture (CFUc) in bone marrow to 40% of the control value on day 1 but CFUc rapidly returned to normal values on day 3. The colony‐forming units in spleen (CFUs): in bone marrow decreased during treatment. On the other hand, CFUc and CFUs in spleen were increased from the initiation of treatment to the time prior to the increase of WBC count. Spleen weight increased after treatment, and histologically, increases of immature and also mature granulocytes and megakaryocytes were observed. However, RA‐700 did not stimulate the progress of hematoprogenitors in vitro. The results indicated that RA‐700 stimulates the progress of hematoprogenitors in the spleen, but this effect is probably indirect. Blackwell Publishing Ltd 1989-03 /pmc/articles/PMC5917711/ /pubmed/2498262 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02307.x Text en
spellingShingle Article
Kato, Taketoshi
Suzumura, Yasuko
Liu, Fen‐Zhi
Tateno, Hiroo
Ogiu, Toshiaki
Ota, Kazuo
Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title_full Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title_fullStr Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title_full_unstemmed Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title_short Leukocytosis in Mice Following Therapy with a Novel Antitumor Agent, RA‐700
title_sort leukocytosis in mice following therapy with a novel antitumor agent, ra‐700
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917711/
https://www.ncbi.nlm.nih.gov/pubmed/2498262
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02307.x
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