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Antineoplastic activity of idazoxan hydrochloride
PURPOSE: Idazoxan hydrochloride (IDA) is a 241 molecular weight imidazoline and adrenoreceptor ligand. It binds to mitochondrial membranes and promotes apoptosis of pancreatic beta cells. Since IDA has not been tested against tumor cells, the purpose of our study was to determine if IDA has antineop...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728905/ https://www.ncbi.nlm.nih.gov/pubmed/19308411 http://dx.doi.org/10.1007/s00280-009-0978-9 |
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author | Eilon, G. F. Weisenthal, L. Stupecky, M. Landucci, G. Slater, L. M. |
author_facet | Eilon, G. F. Weisenthal, L. Stupecky, M. Landucci, G. Slater, L. M. |
author_sort | Eilon, G. F. |
collection | PubMed |
description | PURPOSE: Idazoxan hydrochloride (IDA) is a 241 molecular weight imidazoline and adrenoreceptor ligand. It binds to mitochondrial membranes and promotes apoptosis of pancreatic beta cells. Since IDA has not been tested against tumor cells, the purpose of our study was to determine if IDA has antineoplastic activity. METHODS: We used the conversion of a soluble tetrazolium salt to an insoluble formazan precipitate and differential staining cytotoxicity assays to determine if IDA was cytotoxic to cell lines of murine lung cancer and human prostate cancer, as well as to a variety of fresh human tumor samples. We used flow cytometry to analyze cell death and calreticulin expression. RESULTS: IDA is cytotoxic to both cell lines and against aliquots of specimens of breast, gastric, lung, ovarian and prostate cancers as well as non-Hodgkin’s lymphoma. It produces apoptotic cell death and promotes calreticulin expression, suggesting that IDA might be immunomodulatory in vivo. CONCLUSION: We anticipate that IDA will be clinically useful in cancer treatment. |
format | Text |
id | pubmed-2728905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27289052009-08-20 Antineoplastic activity of idazoxan hydrochloride Eilon, G. F. Weisenthal, L. Stupecky, M. Landucci, G. Slater, L. M. Cancer Chemother Pharmacol Original Article PURPOSE: Idazoxan hydrochloride (IDA) is a 241 molecular weight imidazoline and adrenoreceptor ligand. It binds to mitochondrial membranes and promotes apoptosis of pancreatic beta cells. Since IDA has not been tested against tumor cells, the purpose of our study was to determine if IDA has antineoplastic activity. METHODS: We used the conversion of a soluble tetrazolium salt to an insoluble formazan precipitate and differential staining cytotoxicity assays to determine if IDA was cytotoxic to cell lines of murine lung cancer and human prostate cancer, as well as to a variety of fresh human tumor samples. We used flow cytometry to analyze cell death and calreticulin expression. RESULTS: IDA is cytotoxic to both cell lines and against aliquots of specimens of breast, gastric, lung, ovarian and prostate cancers as well as non-Hodgkin’s lymphoma. It produces apoptotic cell death and promotes calreticulin expression, suggesting that IDA might be immunomodulatory in vivo. CONCLUSION: We anticipate that IDA will be clinically useful in cancer treatment. Springer-Verlag 2009-03-24 2009-11 /pmc/articles/PMC2728905/ /pubmed/19308411 http://dx.doi.org/10.1007/s00280-009-0978-9 Text en © The Author(s) 2009 |
spellingShingle | Original Article Eilon, G. F. Weisenthal, L. Stupecky, M. Landucci, G. Slater, L. M. Antineoplastic activity of idazoxan hydrochloride |
title | Antineoplastic activity of idazoxan hydrochloride |
title_full | Antineoplastic activity of idazoxan hydrochloride |
title_fullStr | Antineoplastic activity of idazoxan hydrochloride |
title_full_unstemmed | Antineoplastic activity of idazoxan hydrochloride |
title_short | Antineoplastic activity of idazoxan hydrochloride |
title_sort | antineoplastic activity of idazoxan hydrochloride |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728905/ https://www.ncbi.nlm.nih.gov/pubmed/19308411 http://dx.doi.org/10.1007/s00280-009-0978-9 |
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