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Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice

BACKGROUND: Although cisplatin is one of the most effective chemotherapeutic agents, cisplatin alone does not achieve a satisfactory therapeutic outcome. Also cisplatin accumulation shows toxicity to normal tissues. In this study, we examined the possibility of HemoHIM both to enhance anticancer eff...

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Autores principales: Park, Hae-Ran, Ju, Eun-Jin, Jo, Sung-Kee, Jung, Uhee, Kim, Sung-Ho, Yee, Sung-Tae
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666758/
https://www.ncbi.nlm.nih.gov/pubmed/19292900
http://dx.doi.org/10.1186/1471-2407-9-85
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author Park, Hae-Ran
Ju, Eun-Jin
Jo, Sung-Kee
Jung, Uhee
Kim, Sung-Ho
Yee, Sung-Tae
author_facet Park, Hae-Ran
Ju, Eun-Jin
Jo, Sung-Kee
Jung, Uhee
Kim, Sung-Ho
Yee, Sung-Tae
author_sort Park, Hae-Ran
collection PubMed
description BACKGROUND: Although cisplatin is one of the most effective chemotherapeutic agents, cisplatin alone does not achieve a satisfactory therapeutic outcome. Also cisplatin accumulation shows toxicity to normal tissues. In this study, we examined the possibility of HemoHIM both to enhance anticancer effect with cisplatin and to reduce the side effects of cisplatin in melanoma-bearing mice. METHODS: HemoHIM was prepared by adding the ethanol-insoluble fraction to the total water extract of a mixture of 3 edible herbs, Angelica Radix, Cnidium Rhizoma and Paeonia Radix. Anticancer effects of HemoHIM with cisplatin were evaluated in melanoma-bearing mice. We used a Cr(51)-release assay to measure the activity of NK/Tc cell and ELISA to evaluate the production of cytokines. RESULTS: In melanoma-bearing mice, cisplatin (4 mg/kg B.W.) reduced the size and weight of the solid tumors, and HemoHIM supplementation with cisplatin enhanced the decrease of both the tumor size (p < 0.1) and weight (p < 0.1). HemoHIM itself did not inhibit melanoma cell growth in vitro, and did not disturb the effects of cisplatin in vitro. However HemoHIM administration enhanced both NK cell and Tc cell activity in mice. Interestingly, HemoHIM increased the proportion of NK cells in the spleen. In melanoma-bearing mice treated with cisplatin, HemoHIM administration also increased the activity of NK cells and Tc cells and the IL-2 and IFN-γ secretion from splenocytes, which seemed to contribute to the enhanced efficacy of cisplatin by HemoHIM. Also, HemoHIM reduced nephrotoxicity as seen by tubular cell of kidney destruction. CONCLUSION: HemoHIM may be a beneficial supplement during cisplatin chemotherapy for enhancing the anti-tumor efficacy and reducing the toxicity of cisplatin.
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spelling pubmed-26667582009-04-08 Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice Park, Hae-Ran Ju, Eun-Jin Jo, Sung-Kee Jung, Uhee Kim, Sung-Ho Yee, Sung-Tae BMC Cancer Research Article BACKGROUND: Although cisplatin is one of the most effective chemotherapeutic agents, cisplatin alone does not achieve a satisfactory therapeutic outcome. Also cisplatin accumulation shows toxicity to normal tissues. In this study, we examined the possibility of HemoHIM both to enhance anticancer effect with cisplatin and to reduce the side effects of cisplatin in melanoma-bearing mice. METHODS: HemoHIM was prepared by adding the ethanol-insoluble fraction to the total water extract of a mixture of 3 edible herbs, Angelica Radix, Cnidium Rhizoma and Paeonia Radix. Anticancer effects of HemoHIM with cisplatin were evaluated in melanoma-bearing mice. We used a Cr(51)-release assay to measure the activity of NK/Tc cell and ELISA to evaluate the production of cytokines. RESULTS: In melanoma-bearing mice, cisplatin (4 mg/kg B.W.) reduced the size and weight of the solid tumors, and HemoHIM supplementation with cisplatin enhanced the decrease of both the tumor size (p < 0.1) and weight (p < 0.1). HemoHIM itself did not inhibit melanoma cell growth in vitro, and did not disturb the effects of cisplatin in vitro. However HemoHIM administration enhanced both NK cell and Tc cell activity in mice. Interestingly, HemoHIM increased the proportion of NK cells in the spleen. In melanoma-bearing mice treated with cisplatin, HemoHIM administration also increased the activity of NK cells and Tc cells and the IL-2 and IFN-γ secretion from splenocytes, which seemed to contribute to the enhanced efficacy of cisplatin by HemoHIM. Also, HemoHIM reduced nephrotoxicity as seen by tubular cell of kidney destruction. CONCLUSION: HemoHIM may be a beneficial supplement during cisplatin chemotherapy for enhancing the anti-tumor efficacy and reducing the toxicity of cisplatin. BioMed Central 2009-03-17 /pmc/articles/PMC2666758/ /pubmed/19292900 http://dx.doi.org/10.1186/1471-2407-9-85 Text en Copyright ©2009 Park et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Park, Hae-Ran
Ju, Eun-Jin
Jo, Sung-Kee
Jung, Uhee
Kim, Sung-Ho
Yee, Sung-Tae
Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title_full Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title_fullStr Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title_full_unstemmed Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title_short Enhanced antitumor efficacy of cisplatin in combination with HemoHIM in tumor-bearing mice
title_sort enhanced antitumor efficacy of cisplatin in combination with hemohim in tumor-bearing mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666758/
https://www.ncbi.nlm.nih.gov/pubmed/19292900
http://dx.doi.org/10.1186/1471-2407-9-85
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