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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Editorial Department of Journal of Biomedical Research
2010
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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. |
format | Online Article Text |
id | pubmed-3596551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Editorial Department of Journal of Biomedical Research |
record_format | MEDLINE/PubMed |
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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