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Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo.
The inability to assess the extent of tumour damage immediately following treatment is a major clinical obstacle to improving the management of cancer patients. Normally, the effectiveness of chemotherapy or radiation therapy cannot be determined for at least several weeks after treatment. We studie...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033672/ https://www.ncbi.nlm.nih.gov/pubmed/7981060 |
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author | Gately, D. P. Jones, J. A. Christen, R. Barton, R. M. Los, G. Howell, S. B. |
author_facet | Gately, D. P. Jones, J. A. Christen, R. Barton, R. M. Los, G. Howell, S. B. |
author_sort | Gately, D. P. |
collection | PubMed |
description | The inability to assess the extent of tumour damage immediately following treatment is a major clinical obstacle to improving the management of cancer patients. Normally, the effectiveness of chemotherapy or radiation therapy cannot be determined for at least several weeks after treatment. We studied the increase in mRNA of the growth arrest and DNA damage-inducible gene GADD153 in human 2008 ovarian carcinoma cells in vitro and in vivo to determine whether treatment-induced increases in the level of GADD153 mRNA could be used as a marker of the extent of tumour damage. GADD153 mRNA was increased in a transient, dose-dependent manner by cisplatin (DDP) when the tumour cells were grown both in vitro and as tumour xenografts in nude mice. The magnitude of induction of GADD153 mRNA did not vary significantly between different 2008 xenografts treated with equal doses of DDP, and GADD153 mRNA induction correlated with the degree of in vitro cytotoxicity for two different schedules of drug exposure. DDP increased GADD153 mRNA levels in melanoma and head and neck xenograft models as well. We conclude that the increase in GADD153 mRNA can be used to detect tumour injury at time points as short as 24 h after administration of DDP. IMAGES: |
format | Text |
id | pubmed-2033672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20336722009-09-10 Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. Gately, D. P. Jones, J. A. Christen, R. Barton, R. M. Los, G. Howell, S. B. Br J Cancer Research Article The inability to assess the extent of tumour damage immediately following treatment is a major clinical obstacle to improving the management of cancer patients. Normally, the effectiveness of chemotherapy or radiation therapy cannot be determined for at least several weeks after treatment. We studied the increase in mRNA of the growth arrest and DNA damage-inducible gene GADD153 in human 2008 ovarian carcinoma cells in vitro and in vivo to determine whether treatment-induced increases in the level of GADD153 mRNA could be used as a marker of the extent of tumour damage. GADD153 mRNA was increased in a transient, dose-dependent manner by cisplatin (DDP) when the tumour cells were grown both in vitro and as tumour xenografts in nude mice. The magnitude of induction of GADD153 mRNA did not vary significantly between different 2008 xenografts treated with equal doses of DDP, and GADD153 mRNA induction correlated with the degree of in vitro cytotoxicity for two different schedules of drug exposure. DDP increased GADD153 mRNA levels in melanoma and head and neck xenograft models as well. We conclude that the increase in GADD153 mRNA can be used to detect tumour injury at time points as short as 24 h after administration of DDP. IMAGES: Nature Publishing Group 1994-12 /pmc/articles/PMC2033672/ /pubmed/7981060 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 Gately, D. P. Jones, J. A. Christen, R. Barton, R. M. Los, G. Howell, S. B. Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title | Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title_full | Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title_fullStr | Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title_full_unstemmed | Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title_short | Induction of the growth arrest and DNA damage-inducible gene GADD153 by cisplatin in vitro and in vivo. |
title_sort | induction of the growth arrest and dna damage-inducible gene gadd153 by cisplatin in vitro and in vivo. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033672/ https://www.ncbi.nlm.nih.gov/pubmed/7981060 |
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