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Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy

BACKGROUND: Chemotherapy with docetaxel (Doc) remains the standard treatment for metastatic and castration-resistance prostate cancer (CRPC). However, the clinical success of Doc is limited by its chemoresistance and side effects. This study investigated whether natural products green tea (GT) and q...

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Autores principales: Wang, Piwen, Henning, Susanne M., Magyar, Clara E., Elshimali, Yahya, Heber, David, Vadgama, Jaydutt V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858851/
https://www.ncbi.nlm.nih.gov/pubmed/27151407
http://dx.doi.org/10.1186/s13046-016-0351-x
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author Wang, Piwen
Henning, Susanne M.
Magyar, Clara E.
Elshimali, Yahya
Heber, David
Vadgama, Jaydutt V.
author_facet Wang, Piwen
Henning, Susanne M.
Magyar, Clara E.
Elshimali, Yahya
Heber, David
Vadgama, Jaydutt V.
author_sort Wang, Piwen
collection PubMed
description BACKGROUND: Chemotherapy with docetaxel (Doc) remains the standard treatment for metastatic and castration-resistance prostate cancer (CRPC). However, the clinical success of Doc is limited by its chemoresistance and side effects. This study investigated whether natural products green tea (GT) and quercetin (Q) enhance the therapeutic efficacy of Doc in CRPC in mouse models. METHODS: Male severe combined immunodeficiency (SCID) mice (n = 10 per group) were inoculated with androgen-independent prostate cancer PC-3 cells subcutaneously. When tumors were established the intervention started. Mice were administered with GT + Q, Doc 5 mg/kg (LD), GT + Q + LD Doc, Doc 10 mg/kg (HD) or control. The concentration of GT polyphenols in brewed tea administered as drinking water was 0.07 % and Q was supplemented in diet at 0.4 %. Doc was intravenously injected weekly for 4 weeks, GT and Q given throughout the study. RESULTS: GT + Q or LD Doc slightly inhibited tumor growth compared to control. However, the combination of GT and Q with LD Doc significantly enhanced the potency of Doc 2-fold and reduced tumor growth by 62 % compared to LD Doc in 7-weeks intervention. A decrease of Ki67 and increase of cleaved caspase 7 were observed in tumors by the mixture, along with lowered blood concentrations of growth factors like VEGF and EGF. The mixture significantly elevated the levels of tumor suppressor mir15a and mir330 in tumor tissues. An increased risk of liver toxicity was only observed with HD Doc treatment. CONCLUSIONS: These results provide a promising regimen to enhance the therapeutic effect of Doc in a less toxic manner.
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spelling pubmed-48588512016-05-07 Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy Wang, Piwen Henning, Susanne M. Magyar, Clara E. Elshimali, Yahya Heber, David Vadgama, Jaydutt V. J Exp Clin Cancer Res Research BACKGROUND: Chemotherapy with docetaxel (Doc) remains the standard treatment for metastatic and castration-resistance prostate cancer (CRPC). However, the clinical success of Doc is limited by its chemoresistance and side effects. This study investigated whether natural products green tea (GT) and quercetin (Q) enhance the therapeutic efficacy of Doc in CRPC in mouse models. METHODS: Male severe combined immunodeficiency (SCID) mice (n = 10 per group) were inoculated with androgen-independent prostate cancer PC-3 cells subcutaneously. When tumors were established the intervention started. Mice were administered with GT + Q, Doc 5 mg/kg (LD), GT + Q + LD Doc, Doc 10 mg/kg (HD) or control. The concentration of GT polyphenols in brewed tea administered as drinking water was 0.07 % and Q was supplemented in diet at 0.4 %. Doc was intravenously injected weekly for 4 weeks, GT and Q given throughout the study. RESULTS: GT + Q or LD Doc slightly inhibited tumor growth compared to control. However, the combination of GT and Q with LD Doc significantly enhanced the potency of Doc 2-fold and reduced tumor growth by 62 % compared to LD Doc in 7-weeks intervention. A decrease of Ki67 and increase of cleaved caspase 7 were observed in tumors by the mixture, along with lowered blood concentrations of growth factors like VEGF and EGF. The mixture significantly elevated the levels of tumor suppressor mir15a and mir330 in tumor tissues. An increased risk of liver toxicity was only observed with HD Doc treatment. CONCLUSIONS: These results provide a promising regimen to enhance the therapeutic effect of Doc in a less toxic manner. BioMed Central 2016-05-06 /pmc/articles/PMC4858851/ /pubmed/27151407 http://dx.doi.org/10.1186/s13046-016-0351-x Text en © Wang et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Piwen
Henning, Susanne M.
Magyar, Clara E.
Elshimali, Yahya
Heber, David
Vadgama, Jaydutt V.
Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title_full Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title_fullStr Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title_full_unstemmed Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title_short Green tea and quercetin sensitize PC-3 xenograft prostate tumors to docetaxel chemotherapy
title_sort green tea and quercetin sensitize pc-3 xenograft prostate tumors to docetaxel chemotherapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858851/
https://www.ncbi.nlm.nih.gov/pubmed/27151407
http://dx.doi.org/10.1186/s13046-016-0351-x
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