Cargando…
Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines
XR5944 (MLN944), a novel bis-phenazine, has demonstrated potent cytotoxic activity against a variety of murine and human tumour models. In the present study, the antitumour activity of XR5944 was investigated in combination with 5-fluorouracil (5-FU) or irinotecan in human colon carcinoma cell lines...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361868/ https://www.ncbi.nlm.nih.gov/pubmed/15700035 http://dx.doi.org/10.1038/sj.bjc.6602403 |
_version_ | 1782153319757643776 |
---|---|
author | Harris, S M Mistry, P Freathy, C Brown, J L Charlton, P A |
author_facet | Harris, S M Mistry, P Freathy, C Brown, J L Charlton, P A |
author_sort | Harris, S M |
collection | PubMed |
description | XR5944 (MLN944), a novel bis-phenazine, has demonstrated potent cytotoxic activity against a variety of murine and human tumour models. In the present study, the antitumour activity of XR5944 was investigated in combination with 5-fluorouracil (5-FU) or irinotecan in human colon carcinoma cell lines and xenografts. In vitro cytotoxicity of the combinations following exposure to the drugs sequentially or simultaneously was evaluated by the sulphorhodamine-B assay and interactions were determined using median-effect analysis. Antagonism was observed (CI>1) following exposure of HT29 cells simultaneously to XR5944 and 5-FU or SN38 (active metabolite of irinotecan). In contrast, sequential exposure of either combination in either order demonstrated at least an additive response (CI⩽1). At least an additive response was also observed with these combinations in HCT116 cells regardless of schedule. Antitumour activity in HT29 xenografts in nude mice was enhanced by sequential administration of 5-FU (65 mg kg(−1)) or irinotecan (CPT-11) (35 mg kg(−1)) 48 h before XR5944 (5, 10, or 15 mg kg(−1)) compared to single agent treatment at the same or higher doses. Administration of irinotecan (35 mg kg(−1)) and XR5944 (15 mg kg(−1)) just 30 min apart yielded similar efficacy to sequential administration 48 h apart. All combinations were well tolerated. These data suggest that combinations of XR5944 with irinotecan or 5-FU are of significant interest in the treatment of colon cancer. |
format | Text |
id | pubmed-2361868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23618682009-09-10 Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines Harris, S M Mistry, P Freathy, C Brown, J L Charlton, P A Br J Cancer Translational Therapeutics XR5944 (MLN944), a novel bis-phenazine, has demonstrated potent cytotoxic activity against a variety of murine and human tumour models. In the present study, the antitumour activity of XR5944 was investigated in combination with 5-fluorouracil (5-FU) or irinotecan in human colon carcinoma cell lines and xenografts. In vitro cytotoxicity of the combinations following exposure to the drugs sequentially or simultaneously was evaluated by the sulphorhodamine-B assay and interactions were determined using median-effect analysis. Antagonism was observed (CI>1) following exposure of HT29 cells simultaneously to XR5944 and 5-FU or SN38 (active metabolite of irinotecan). In contrast, sequential exposure of either combination in either order demonstrated at least an additive response (CI⩽1). At least an additive response was also observed with these combinations in HCT116 cells regardless of schedule. Antitumour activity in HT29 xenografts in nude mice was enhanced by sequential administration of 5-FU (65 mg kg(−1)) or irinotecan (CPT-11) (35 mg kg(−1)) 48 h before XR5944 (5, 10, or 15 mg kg(−1)) compared to single agent treatment at the same or higher doses. Administration of irinotecan (35 mg kg(−1)) and XR5944 (15 mg kg(−1)) just 30 min apart yielded similar efficacy to sequential administration 48 h apart. All combinations were well tolerated. These data suggest that combinations of XR5944 with irinotecan or 5-FU are of significant interest in the treatment of colon cancer. Nature Publishing Group 2005-02-28 2005-02-08 /pmc/articles/PMC2361868/ /pubmed/15700035 http://dx.doi.org/10.1038/sj.bjc.6602403 Text en Copyright © 2005 Cancer Research UK 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 | Translational Therapeutics Harris, S M Mistry, P Freathy, C Brown, J L Charlton, P A Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title | Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title_full | Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title_fullStr | Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title_full_unstemmed | Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title_short | Antitumour activity of XR5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
title_sort | antitumour activity of xr5944 in vitro and in vivo in combination with 5-fluorouracil and irinotecan in colon cancer cell lines |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361868/ https://www.ncbi.nlm.nih.gov/pubmed/15700035 http://dx.doi.org/10.1038/sj.bjc.6602403 |
work_keys_str_mv | AT harrissm antitumouractivityofxr5944invitroandinvivoincombinationwith5fluorouracilandirinotecanincoloncancercelllines AT mistryp antitumouractivityofxr5944invitroandinvivoincombinationwith5fluorouracilandirinotecanincoloncancercelllines AT freathyc antitumouractivityofxr5944invitroandinvivoincombinationwith5fluorouracilandirinotecanincoloncancercelllines AT brownjl antitumouractivityofxr5944invitroandinvivoincombinationwith5fluorouracilandirinotecanincoloncancercelllines AT charltonpa antitumouractivityofxr5944invitroandinvivoincombinationwith5fluorouracilandirinotecanincoloncancercelllines |