Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice

Background: The previous studies have demonstrated that the polysaccharide isolated from Tarphochlamys affinis (PTA) exhibits anti-tumor effect on S180 tumor-bearing mice and protective effects against hepatic injury. Methods: In this study, we investigated the anti-tumor activity and possible under...

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Main Authors: Xiaojun Tang, Jianchun Huang, Hao Xiong, Keyuan Zhang, Chunxia Chen, Xiaojie Wei, Xiaohui Xu, Qiuqiao Xie, Renbin Huang
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2016-08-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:http://www.karger.com/Article/FullText/447811
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author Xiaojun Tang
Jianchun Huang
Hao Xiong
Keyuan Zhang
Chunxia Chen
Xiaojie Wei
Xiaohui Xu
Qiuqiao Xie
Renbin Huang
author_facet Xiaojun Tang
Jianchun Huang
Hao Xiong
Keyuan Zhang
Chunxia Chen
Xiaojie Wei
Xiaohui Xu
Qiuqiao Xie
Renbin Huang
author_sort Xiaojun Tang
collection DOAJ
description Background: The previous studies have demonstrated that the polysaccharide isolated from Tarphochlamys affinis (PTA) exhibits anti-tumor effect on S180 tumor-bearing mice and protective effects against hepatic injury. Methods: In this study, we investigated the anti-tumor activity and possible underlying mechanism of PTA on liver cancer using a murine H22 hepatocarcinoma model. Results: PTA was capable of repressing transplanted H22 solid hepatic tumor cell growth in vivo. The relative weight of immune organs (spleen and thymus) and lymphocyte proliferation induced by ConA or LPS were improved after PTA treatment. Furthermore, treatment with PTA promoted immune-stimulating serum cytokine secretion in H22 tumor-bearing mice. Additionally, the percentage of CD4+ T lymphocytes, CD8+ T lymphocytes and NK cells was increased in tumor-bearing mice following PTA administration. In tumor tissue, PTA significantly up-regulated the expression of Bax and p53 proteins and down-regulated the expression of Bcl-2 protein. In addition, at the therapeutic dose, PTA displayed very few toxic effects to major organs, such as the liver and kidney, in tumor-bearing mice. Conclusion: In H22 tumor-bearing mice, PTA exhibited prominent anti-tumor activity in vivo. The possible mechanism of action might be related to enhanced host immune system function and induction of H22 tumor cell apoptosis.
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spelling doaj.art-c20c095e29eb47d5bf65b27e8a9127a92022-12-21T17:56:17ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782016-08-013931040105010.1159/000447811447811Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing MiceXiaojun TangJianchun HuangHao XiongKeyuan ZhangChunxia ChenXiaojie WeiXiaohui XuQiuqiao XieRenbin HuangBackground: The previous studies have demonstrated that the polysaccharide isolated from Tarphochlamys affinis (PTA) exhibits anti-tumor effect on S180 tumor-bearing mice and protective effects against hepatic injury. Methods: In this study, we investigated the anti-tumor activity and possible underlying mechanism of PTA on liver cancer using a murine H22 hepatocarcinoma model. Results: PTA was capable of repressing transplanted H22 solid hepatic tumor cell growth in vivo. The relative weight of immune organs (spleen and thymus) and lymphocyte proliferation induced by ConA or LPS were improved after PTA treatment. Furthermore, treatment with PTA promoted immune-stimulating serum cytokine secretion in H22 tumor-bearing mice. Additionally, the percentage of CD4+ T lymphocytes, CD8+ T lymphocytes and NK cells was increased in tumor-bearing mice following PTA administration. In tumor tissue, PTA significantly up-regulated the expression of Bax and p53 proteins and down-regulated the expression of Bcl-2 protein. In addition, at the therapeutic dose, PTA displayed very few toxic effects to major organs, such as the liver and kidney, in tumor-bearing mice. Conclusion: In H22 tumor-bearing mice, PTA exhibited prominent anti-tumor activity in vivo. The possible mechanism of action might be related to enhanced host immune system function and induction of H22 tumor cell apoptosis.http://www.karger.com/Article/FullText/447811PolysaccharideAnti-tumorTarphochlamys affinis (Acanthaceae)Hepatocarcinoma
spellingShingle Xiaojun Tang
Jianchun Huang
Hao Xiong
Keyuan Zhang
Chunxia Chen
Xiaojie Wei
Xiaohui Xu
Qiuqiao Xie
Renbin Huang
Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
Cellular Physiology and Biochemistry
Polysaccharide
Anti-tumor
Tarphochlamys affinis (Acanthaceae)
Hepatocarcinoma
title Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
title_full Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
title_fullStr Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
title_full_unstemmed Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
title_short Anti-Tumor Effects of the Polysaccharide Isolated from Tarphochlamys Affinis in H22 Tumor-Bearing Mice
title_sort anti tumor effects of the polysaccharide isolated from tarphochlamys affinis in h22 tumor bearing mice
topic Polysaccharide
Anti-tumor
Tarphochlamys affinis (Acanthaceae)
Hepatocarcinoma
url http://www.karger.com/Article/FullText/447811
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