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A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein

A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein
A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein
In this study, one homogeneous polysaccharide (SP1), with a molecular weight of 56 kDa, was isolated from the Huaier fruiting bodies. It had a backbone consisting of 1, 4-linked-?-D-Galp and 1, 3, 6-linked-?-D-Galp residues, which was terminated with 1-linked-?-D-Glcp and 1-linked-?-L-Araf terminal at O-3 position of 1, 3, 6-linked-?-D-Galp unit along the main chain in the ratio of 1.1: 2.0: 1.1: 1.1. MTT assay showed that shMTDH or SP1 (100, 200 and 400 ?g/ml) was able to suppress the proliferation of MCF-7 cells, due to a significant increase in the number of apoptotic cells as determined by flow cytometric analysis. Furthermore, Western blot analysis revealed that SP1 or shMTDH treatment led to a rise of ratio between proapoptotic Bax and antiapoptotic Bcl-2 protein in MCF-7 cells. In addition, carcinogene MTDH protein expression in MCF-7 cells received SP1 (100, 200 and 400 ?g/ml) or shMTDH treatment was also repressed after 48 h incubation. Taken together, these findings indicated that SP1 has anticancer potential in the treatment of human breast cancer
0144-8617
1-34
Luo, Zhiyong
c770d311-3ca9-41de-8ce9-f560a0ed79b1
Hu, Xiaopeng
da058c6e-76c5-454a-aef5-141cf2407859
Xiong, Hua
f80e5b10-9793-40ae-8143-1762577028f4
Qiu, Hong
dc13a95d-9523-43de-94c3-ddd4ff9809aa
Yuan, Xianglin
54dfb6d3-78bf-48da-936d-ded37bfcf238
Zhu, Feng
a9499a5c-c42b-4fc0-91dd-0a7f830e6ce0
Wang, Yihua
f5044a95-60a7-42d2-87d6-5f1f789e3a7e
Zou, Yanmei
6783820d-2ff0-4900-9ade-34fe1180f56f
Luo, Zhiyong
c770d311-3ca9-41de-8ce9-f560a0ed79b1
Hu, Xiaopeng
da058c6e-76c5-454a-aef5-141cf2407859
Xiong, Hua
f80e5b10-9793-40ae-8143-1762577028f4
Qiu, Hong
dc13a95d-9523-43de-94c3-ddd4ff9809aa
Yuan, Xianglin
54dfb6d3-78bf-48da-936d-ded37bfcf238
Zhu, Feng
a9499a5c-c42b-4fc0-91dd-0a7f830e6ce0
Wang, Yihua
f5044a95-60a7-42d2-87d6-5f1f789e3a7e
Zou, Yanmei
6783820d-2ff0-4900-9ade-34fe1180f56f

Luo, Zhiyong, Hu, Xiaopeng, Xiong, Hua, Qiu, Hong, Yuan, Xianglin, Zhu, Feng, Wang, Yihua and Zou, Yanmei (2016) A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein. Carbohydrate Polymers, 1-34. (doi:10.1016/j.carbpol.2016.06.046).

Record type: Article

Abstract

In this study, one homogeneous polysaccharide (SP1), with a molecular weight of 56 kDa, was isolated from the Huaier fruiting bodies. It had a backbone consisting of 1, 4-linked-?-D-Galp and 1, 3, 6-linked-?-D-Galp residues, which was terminated with 1-linked-?-D-Glcp and 1-linked-?-L-Araf terminal at O-3 position of 1, 3, 6-linked-?-D-Galp unit along the main chain in the ratio of 1.1: 2.0: 1.1: 1.1. MTT assay showed that shMTDH or SP1 (100, 200 and 400 ?g/ml) was able to suppress the proliferation of MCF-7 cells, due to a significant increase in the number of apoptotic cells as determined by flow cytometric analysis. Furthermore, Western blot analysis revealed that SP1 or shMTDH treatment led to a rise of ratio between proapoptotic Bax and antiapoptotic Bcl-2 protein in MCF-7 cells. In addition, carcinogene MTDH protein expression in MCF-7 cells received SP1 (100, 200 and 400 ?g/ml) or shMTDH treatment was also repressed after 48 h incubation. Taken together, these findings indicated that SP1 has anticancer potential in the treatment of human breast cancer

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Accepted/In Press date: 11 June 2016
e-pub ahead of print date: 14 July 2016
Organisations: Biomedicine

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Local EPrints ID: 397085
URI: http://eprints.soton.ac.uk/id/eprint/397085
ISSN: 0144-8617
PURE UUID: f96a337c-839e-4c70-a3db-4198f27b09bc
ORCID for Yihua Wang: ORCID iD orcid.org/0000-0001-5561-0648

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Date deposited: 20 Jun 2016 09:33
Last modified: 15 Mar 2024 05:41

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Contributors

Author: Zhiyong Luo
Author: Xiaopeng Hu
Author: Hua Xiong
Author: Hong Qiu
Author: Xianglin Yuan
Author: Feng Zhu
Author: Yihua Wang ORCID iD
Author: Yanmei Zou

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