Cargando…

Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea

PURPOSE: To investigate whether clinically relevant levels of epigallocatechin gallate (EGCG, a component of green tea) or vitamin C (ascorbic acid) could antagonize bortezomib antitumor activity in CWR22 human prostate xenograft tumors. METHODS: The pharmacokinetics (PK) of EGCG and ascorbic acid w...

Descripción completa

Detalles Bibliográficos
Autores principales: Bannerman, Bret, Xu, Ling, Jones, Matthew, Tsu, Christopher, Yu, Jie, Hales, Paul, Monbaliu, Johan, Fleming, Paul, Dick, Lawrence, Manfredi, Mark, Claiborne, Christopher, Bolen, Joseph, Kupperman, Erik, Berger, Allison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215871/
https://www.ncbi.nlm.nih.gov/pubmed/21400028
http://dx.doi.org/10.1007/s00280-011-1591-2
_version_ 1782216437445689344
author Bannerman, Bret
Xu, Ling
Jones, Matthew
Tsu, Christopher
Yu, Jie
Hales, Paul
Monbaliu, Johan
Fleming, Paul
Dick, Lawrence
Manfredi, Mark
Claiborne, Christopher
Bolen, Joseph
Kupperman, Erik
Berger, Allison
author_facet Bannerman, Bret
Xu, Ling
Jones, Matthew
Tsu, Christopher
Yu, Jie
Hales, Paul
Monbaliu, Johan
Fleming, Paul
Dick, Lawrence
Manfredi, Mark
Claiborne, Christopher
Bolen, Joseph
Kupperman, Erik
Berger, Allison
author_sort Bannerman, Bret
collection PubMed
description PURPOSE: To investigate whether clinically relevant levels of epigallocatechin gallate (EGCG, a component of green tea) or vitamin C (ascorbic acid) could antagonize bortezomib antitumor activity in CWR22 human prostate xenograft tumors. METHODS: The pharmacokinetics (PK) of EGCG and ascorbic acid were determined in immunocompromised mice and compared with concentrations measured in human PK studies of dietary supplements. Antitumor activity of bortezomib in combination with EGCG or ascorbic acid was determined using several dosing regimens to evaluate different target plasma concentrations of EGCG and ascorbic acid. RESULTS: Bortezomib dosed twice-weekly at 0.8 mg/kg IV demonstrated tumor growth inhibition (TGI) of 53.9–58.9%. However, when combined with EGCG such that the plasma concentrations of EGCG were >200 μM at the time of bortezomib dosing, all antitumor activity was abrogated (TGI = −17.7%). A lower concentration of EGCG (11–16 μM), which is severalfold higher than measured clinically in humans taking EGCG supplements (0.6–3 μM), was not antagonistic to bortezomib (TGI 63.5%). Pharmacodynamic studies of proteasome inhibition reflected these findings. Ascorbic acid (40 and 500 mg/kg PO daily) was evaluated under a similar study design and did not antagonize bortezomib antitumor activity (TGI 57.2 and 72.2%). CONCLUSIONS: No antagonism of bortezomib is seen in preclinical in vivo experiments, where EGCG or ascorbic acid plasma concentrations are commensurate with dietary or supplemental intake. The data suggest that patients receiving bortezomib treatment do not need to avoid normal dietary consumption of green tea, vitamin C-containing foods, or EGCG or vitamin C dietary supplements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00280-011-1591-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-3215871
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Springer-Verlag
record_format MEDLINE/PubMed
spelling pubmed-32158712011-12-09 Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea Bannerman, Bret Xu, Ling Jones, Matthew Tsu, Christopher Yu, Jie Hales, Paul Monbaliu, Johan Fleming, Paul Dick, Lawrence Manfredi, Mark Claiborne, Christopher Bolen, Joseph Kupperman, Erik Berger, Allison Cancer Chemother Pharmacol Original Article PURPOSE: To investigate whether clinically relevant levels of epigallocatechin gallate (EGCG, a component of green tea) or vitamin C (ascorbic acid) could antagonize bortezomib antitumor activity in CWR22 human prostate xenograft tumors. METHODS: The pharmacokinetics (PK) of EGCG and ascorbic acid were determined in immunocompromised mice and compared with concentrations measured in human PK studies of dietary supplements. Antitumor activity of bortezomib in combination with EGCG or ascorbic acid was determined using several dosing regimens to evaluate different target plasma concentrations of EGCG and ascorbic acid. RESULTS: Bortezomib dosed twice-weekly at 0.8 mg/kg IV demonstrated tumor growth inhibition (TGI) of 53.9–58.9%. However, when combined with EGCG such that the plasma concentrations of EGCG were >200 μM at the time of bortezomib dosing, all antitumor activity was abrogated (TGI = −17.7%). A lower concentration of EGCG (11–16 μM), which is severalfold higher than measured clinically in humans taking EGCG supplements (0.6–3 μM), was not antagonistic to bortezomib (TGI 63.5%). Pharmacodynamic studies of proteasome inhibition reflected these findings. Ascorbic acid (40 and 500 mg/kg PO daily) was evaluated under a similar study design and did not antagonize bortezomib antitumor activity (TGI 57.2 and 72.2%). CONCLUSIONS: No antagonism of bortezomib is seen in preclinical in vivo experiments, where EGCG or ascorbic acid plasma concentrations are commensurate with dietary or supplemental intake. The data suggest that patients receiving bortezomib treatment do not need to avoid normal dietary consumption of green tea, vitamin C-containing foods, or EGCG or vitamin C dietary supplements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00280-011-1591-2) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-03-13 2011 /pmc/articles/PMC3215871/ /pubmed/21400028 http://dx.doi.org/10.1007/s00280-011-1591-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Bannerman, Bret
Xu, Ling
Jones, Matthew
Tsu, Christopher
Yu, Jie
Hales, Paul
Monbaliu, Johan
Fleming, Paul
Dick, Lawrence
Manfredi, Mark
Claiborne, Christopher
Bolen, Joseph
Kupperman, Erik
Berger, Allison
Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title_full Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title_fullStr Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title_full_unstemmed Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title_short Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea
title_sort preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin c or with epigallocatechin gallate, a component of green tea
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215871/
https://www.ncbi.nlm.nih.gov/pubmed/21400028
http://dx.doi.org/10.1007/s00280-011-1591-2
work_keys_str_mv AT bannermanbret preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT xuling preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT jonesmatthew preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT tsuchristopher preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT yujie preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT halespaul preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT monbaliujohan preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT flemingpaul preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT dicklawrence preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT manfredimark preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT claibornechristopher preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT bolenjoseph preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT kuppermanerik preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea
AT bergerallison preclinicalevaluationoftheantitumoractivityofbortezomibincombinationwithvitamincorwithepigallocatechingallateacomponentofgreentea