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In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()

OBJECTIVE: To investigate the synergistic anti-tumor effect of QHF (a Chinese medicine formula with anti-tumor active ingredients, including 800 mg/kg Cinobufotalin, 14 mg/kg Ginsenoside Rg3, 5.5 mg/kg Notoginseng and 100 mg/kg Lentinan) when combined with the chemotherapy drug cisplatin (DDP). METH...

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Autores principales: Tao, Chen, Dan, Li, ling, Fuya, Peng, Gongzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596551/
https://www.ncbi.nlm.nih.gov/pubmed/23554627
http://dx.doi.org/10.1016/S1674-8301(10)60025-5
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author Tao, Chen
Dan, Li
ling, Fuya
Peng, Gongzi
author_facet Tao, Chen
Dan, Li
ling, Fuya
Peng, Gongzi
author_sort Tao, Chen
collection PubMed
description OBJECTIVE: To investigate the synergistic anti-tumor effect of QHF (a Chinese medicine formula with anti-tumor active ingredients, including 800 mg/kg Cinobufotalin, 14 mg/kg Ginsenoside Rg3, 5.5 mg/kg Notoginseng and 100 mg/kg Lentinan) when combined with the chemotherapy drug cisplatin (DDP). METHODS: Hepatocellular carcinoma H(22) cells were implanted into mice and after the transplants were successfully established the animals were divided into four groups, namely a normal saline(NS) control group, QHF group, DDP group and QHF+DDP group. The tumor growth was monitored and the survival time determined. In vitro studies employing H(22) cells used the first three groups, and determined the effects of QHF and DDP on tumor cell cycle distribution, apoptosis and morphologic changes in vitro. RESULTS: QHF significantly inhibited the growth of tumors and prolonged the survival time of mice with hepatocellular carcinomas. QHF combined with DDP could attenuate DDP-induced leucopenia, spleen and thymus atrophy and other indicators of toxicity. The inhibition rate of tumor growth reached 82.54% with QHF+DDP, and QHF prolonged the life span of DDP-treated mice by 66.83%. In the in vitro experiments tumor cells showed morphological changes characteristic of apoptosis by both light and transmission electron microscopy in the QHF group, and the apoptosis rate was 33.85%. Moreover, the proportion of cells in the G(0)/G(1) phase was increased and those in the S-phase decreased. CONCLUSION: QHF combined with DDP could significantly inhibit tumor growth, induce the apoptosis of tumor cells and effectively attenuate DDP toxicity.
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spelling pubmed-35965512013-04-02 In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma() Tao, Chen Dan, Li ling, Fuya Peng, Gongzi J Biomed Res Research Paper OBJECTIVE: To investigate the synergistic anti-tumor effect of QHF (a Chinese medicine formula with anti-tumor active ingredients, including 800 mg/kg Cinobufotalin, 14 mg/kg Ginsenoside Rg3, 5.5 mg/kg Notoginseng and 100 mg/kg Lentinan) when combined with the chemotherapy drug cisplatin (DDP). METHODS: Hepatocellular carcinoma H(22) cells were implanted into mice and after the transplants were successfully established the animals were divided into four groups, namely a normal saline(NS) control group, QHF group, DDP group and QHF+DDP group. The tumor growth was monitored and the survival time determined. In vitro studies employing H(22) cells used the first three groups, and determined the effects of QHF and DDP on tumor cell cycle distribution, apoptosis and morphologic changes in vitro. RESULTS: QHF significantly inhibited the growth of tumors and prolonged the survival time of mice with hepatocellular carcinomas. QHF combined with DDP could attenuate DDP-induced leucopenia, spleen and thymus atrophy and other indicators of toxicity. The inhibition rate of tumor growth reached 82.54% with QHF+DDP, and QHF prolonged the life span of DDP-treated mice by 66.83%. In the in vitro experiments tumor cells showed morphological changes characteristic of apoptosis by both light and transmission electron microscopy in the QHF group, and the apoptosis rate was 33.85%. Moreover, the proportion of cells in the G(0)/G(1) phase was increased and those in the S-phase decreased. CONCLUSION: QHF combined with DDP could significantly inhibit tumor growth, induce the apoptosis of tumor cells and effectively attenuate DDP toxicity. Editorial Department of Journal of Biomedical Research 2010-03 /pmc/articles/PMC3596551/ /pubmed/23554627 http://dx.doi.org/10.1016/S1674-8301(10)60025-5 Text en © 2010 by the Journal of Biomedical Research. All rights reserved. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Research Paper
Tao, Chen
Dan, Li
ling, Fuya
Peng, Gongzi
In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title_full In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title_fullStr In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title_full_unstemmed In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title_short In vivo and in vitro effects of QHF combined with chemotherapy on hepatocellular carcinoma()
title_sort in vivo and in vitro effects of qhf combined with chemotherapy on hepatocellular carcinoma()
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596551/
https://www.ncbi.nlm.nih.gov/pubmed/23554627
http://dx.doi.org/10.1016/S1674-8301(10)60025-5
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