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Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16.
The antibiotic drug novobiocin was evaluated for its anti-tumour properties in B16 melanoma cells. Novobiocin is shown to inhibit melanoma B16 cell proliferation. The anti-proliferative effect was gradually reversible upon removal of novobiocin from the culture medium. Growth inhibition by novobioci...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977725/ https://www.ncbi.nlm.nih.gov/pubmed/1739614 |
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author | Nordenberg, J. Albukrek, D. Hadar, T. Fux, A. Wasserman, L. Novogrodsky, A. Sidi, Y. |
author_facet | Nordenberg, J. Albukrek, D. Hadar, T. Fux, A. Wasserman, L. Novogrodsky, A. Sidi, Y. |
author_sort | Nordenberg, J. |
collection | PubMed |
description | The antibiotic drug novobiocin was evaluated for its anti-tumour properties in B16 melanoma cells. Novobiocin is shown to inhibit melanoma B16 cell proliferation. The anti-proliferative effect was gradually reversible upon removal of novobiocin from the culture medium. Growth inhibition by novobiocin was accompanied by phenotypic alterations, that included morphological changes, lipid accumulation and marked increases in the activities of NADPH cytochrome c reductase and gamma glutamyl transpeptidase. In vivo administration of repeated i.p. doses of novobiocin, to mice implanted with B16 melanoma cells resulted in growth retardation. The combined treatment of the B16 melanoma cells with novobiocin and other chemical inducers of differentiation was examined in a cell growth assay. Novobiocin and sodium butyrate inhibited cell growth in a near additive manner, while combination of novobiocin with the GTP-depleting agents, tiazofurin or mycophenolic acid resulted in a synergistic decrease in cell growth. Our results support the contention further that novobiocin and other differentiating agents might be of potential value in melanoma therapy. IMAGES: |
format | Text |
id | pubmed-1977725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19777252009-09-10 Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. Nordenberg, J. Albukrek, D. Hadar, T. Fux, A. Wasserman, L. Novogrodsky, A. Sidi, Y. Br J Cancer Research Article The antibiotic drug novobiocin was evaluated for its anti-tumour properties in B16 melanoma cells. Novobiocin is shown to inhibit melanoma B16 cell proliferation. The anti-proliferative effect was gradually reversible upon removal of novobiocin from the culture medium. Growth inhibition by novobiocin was accompanied by phenotypic alterations, that included morphological changes, lipid accumulation and marked increases in the activities of NADPH cytochrome c reductase and gamma glutamyl transpeptidase. In vivo administration of repeated i.p. doses of novobiocin, to mice implanted with B16 melanoma cells resulted in growth retardation. The combined treatment of the B16 melanoma cells with novobiocin and other chemical inducers of differentiation was examined in a cell growth assay. Novobiocin and sodium butyrate inhibited cell growth in a near additive manner, while combination of novobiocin with the GTP-depleting agents, tiazofurin or mycophenolic acid resulted in a synergistic decrease in cell growth. Our results support the contention further that novobiocin and other differentiating agents might be of potential value in melanoma therapy. IMAGES: Nature Publishing Group 1992-02 /pmc/articles/PMC1977725/ /pubmed/1739614 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Nordenberg, J. Albukrek, D. Hadar, T. Fux, A. Wasserman, L. Novogrodsky, A. Sidi, Y. Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title | Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title_full | Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title_fullStr | Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title_full_unstemmed | Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title_short | Novobiocin-induced anti-proliferative and differentiating effects in melanoma B16. |
title_sort | novobiocin-induced anti-proliferative and differentiating effects in melanoma b16. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977725/ https://www.ncbi.nlm.nih.gov/pubmed/1739614 |
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