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...
Main Authors: | , , , , , , , , |
---|---|
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 |
_version_ | 1819213306248822784 |
---|---|
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. |
first_indexed | 2024-12-23T06:56:46Z |
format | Article |
id | doaj.art-c20c095e29eb47d5bf65b27e8a9127a9 |
institution | Directory Open Access Journal |
issn | 1015-8987 1421-9778 |
language | English |
last_indexed | 2024-12-23T06:56:46Z |
publishDate | 2016-08-01 |
publisher | Cell Physiol Biochem Press GmbH & Co KG |
record_format | Article |
series | Cellular Physiology and Biochemistry |
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 |
work_keys_str_mv | AT xiaojuntang antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT jianchunhuang antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT haoxiong antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT keyuanzhang antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT chunxiachen antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT xiaojiewei antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT xiaohuixu antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT qiuqiaoxie antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice AT renbinhuang antitumoreffectsofthepolysaccharideisolatedfromtarphochlamysaffinisinh22tumorbearingmice |