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Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice

A fluorine‐containing anthracyctine, ME2303, given intravenously once a week for 4 weeks at the maximum tolerated dose showed better therapeutic effects against 2 gastric, 3 lung and 2 human breast tumor xenografts than did adriamycin (ADM) at the maximum tolerated dose. Among the tumors, ME2303 sho...

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Detalles Bibliográficos
Autores principales: Tsuruo, Takashi, Sato, Shigeo, Yusa, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917819/
https://www.ncbi.nlm.nih.gov/pubmed/2507492
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01697.x
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author Tsuruo, Takashi
Sato, Shigeo
Yusa, Keisuke
author_facet Tsuruo, Takashi
Sato, Shigeo
Yusa, Keisuke
author_sort Tsuruo, Takashi
collection PubMed
description A fluorine‐containing anthracyctine, ME2303, given intravenously once a week for 4 weeks at the maximum tolerated dose showed better therapeutic effects against 2 gastric, 3 lung and 2 human breast tumor xenografts than did adriamycin (ADM) at the maximum tolerated dose. Among the tumors, ME2303 showed a better effect against St‐40, a well‐differentiated human gastric adenocarcinoma, against which ADM showed only a marginal effect. Likewise, ME2303 was more effective against Lu‐24 human small cell carcinoma and MX‐1 human medullary tubular adenocarcinoma than ADM. Notably, the Lu‐24 tumor, developed in nude mice, disappeared after the treatment in 3 out of 6 mice. ME2303 would be an interesting compound for phase I and II clinical studies in the future
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spelling pubmed-59178192018-05-11 Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice Tsuruo, Takashi Sato, Shigeo Yusa, Keisuke Jpn J Cancer Res Article A fluorine‐containing anthracyctine, ME2303, given intravenously once a week for 4 weeks at the maximum tolerated dose showed better therapeutic effects against 2 gastric, 3 lung and 2 human breast tumor xenografts than did adriamycin (ADM) at the maximum tolerated dose. Among the tumors, ME2303 showed a better effect against St‐40, a well‐differentiated human gastric adenocarcinoma, against which ADM showed only a marginal effect. Likewise, ME2303 was more effective against Lu‐24 human small cell carcinoma and MX‐1 human medullary tubular adenocarcinoma than ADM. Notably, the Lu‐24 tumor, developed in nude mice, disappeared after the treatment in 3 out of 6 mice. ME2303 would be an interesting compound for phase I and II clinical studies in the future Blackwell Publishing Ltd 1989-07 /pmc/articles/PMC5917819/ /pubmed/2507492 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01697.x Text en
spellingShingle Article
Tsuruo, Takashi
Sato, Shigeo
Yusa, Keisuke
Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title_full Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title_fullStr Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title_full_unstemmed Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title_short Antitumor Activity of ME2303, a Fluorine‐containing Anthracycline, against Human Tumors Implanted in Nude Mice
title_sort antitumor activity of me2303, a fluorine‐containing anthracycline, against human tumors implanted in nude mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917819/
https://www.ncbi.nlm.nih.gov/pubmed/2507492
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01697.x
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