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The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture

The effects of vincristine (VCR) and doxorubicin (DOX) on the growth of an established line of human lung cancer cells, PC9, were studied in methylcellulose and suspension cultures. The secondary colony formation in methylcellulose and recovery of clonogenic cells in suspension were considered to re...

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Detalles Bibliográficos
Autores principales: Yamashita, Yoko, Nara, Nobuo, Aoki, Nobuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917725/
https://www.ncbi.nlm.nih.gov/pubmed/2498261
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02305.x
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author Yamashita, Yoko
Nara, Nobuo
Aoki, Nobuo
author_facet Yamashita, Yoko
Nara, Nobuo
Aoki, Nobuo
author_sort Yamashita, Yoko
collection PubMed
description The effects of vincristine (VCR) and doxorubicin (DOX) on the growth of an established line of human lung cancer cells, PC9, were studied in methylcellulose and suspension cultures. The secondary colony formation in methylcellulose and recovery of clonogenic cells in suspension were considered to reflect well the self‐renewal of the clonogenic cells. When dose‐response curves were obtained for VCR and DOX, the primary clonogenic cells (PE1) were more sensitive than secondary clonogenic cells (PE2) or clonogenic cells in suspension. Repeated exposure to VCR in suspension did not inhibit the exponential growth of the clonogenic cells. These data indicated that both drugs were relatively ineffective in specifically suppressing the self‐renewal of the clonogenic cells.
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spelling pubmed-59177252018-05-11 The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture Yamashita, Yoko Nara, Nobuo Aoki, Nobuo Jpn J Cancer Res Article The effects of vincristine (VCR) and doxorubicin (DOX) on the growth of an established line of human lung cancer cells, PC9, were studied in methylcellulose and suspension cultures. The secondary colony formation in methylcellulose and recovery of clonogenic cells in suspension were considered to reflect well the self‐renewal of the clonogenic cells. When dose‐response curves were obtained for VCR and DOX, the primary clonogenic cells (PE1) were more sensitive than secondary clonogenic cells (PE2) or clonogenic cells in suspension. Repeated exposure to VCR in suspension did not inhibit the exponential growth of the clonogenic cells. These data indicated that both drugs were relatively ineffective in specifically suppressing the self‐renewal of the clonogenic cells. Blackwell Publishing Ltd 1989-03 /pmc/articles/PMC5917725/ /pubmed/2498261 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02305.x Text en
spellingShingle Article
Yamashita, Yoko
Nara, Nobuo
Aoki, Nobuo
The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title_full The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title_fullStr The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title_full_unstemmed The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title_short The Effects of Vincristine and Doxorubicin on the Clonogenic Cells of a Human Lung Cancer Cell Line in Methylcellulose and Suspension Culture
title_sort effects of vincristine and doxorubicin on the clonogenic cells of a human lung cancer cell line in methylcellulose and suspension culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917725/
https://www.ncbi.nlm.nih.gov/pubmed/2498261
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02305.x
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