A polysaccharide from Huaier induced apoptosis in MCF-7 breast cancer cells via down-regulation of MTDH protein. (20th October 2016)

• Record Type: Journal Article
• Authors: Luo, Zhiyong; Hu, Xiaopeng; Xiong, Hua; Qiu, Hong; Yuan, Xianglin; Zhu, Feng; Wang, Yihua; Zou, Yanmei
• Is Part Of: Carbohydrate polymers. Volume 151(2016)
• Page Start: 1027
• Page End: 1033
• Publication Date: 2016-10-20
• Subjects: Huaier polysaccharide -- Breast cancer -- MTDH -- Apoptosis; Polysaccharides -- Periodicals; Polysaccharides -- Periodicals; Polysaccharides -- Périodiques; Electronic journals; 547.78
• DOI: 10.1016/j.carbpol.2016.06.046
• Languages: English
• ISSNs: 0144-8617

Abstract

Highlights: A polysaccharide SP1 was purified from Huaier fruiting bodies. The chemical properties and sugar linkage of SP1 were evaluated. SP1 inhibited the proliferation of MCF-7 cells by inducing apoptosis. SP1 treatment led to a rise of Bax/Bcl-2 ratio in MCF-7 cells. SP1 treatment repressed MTDH protein expression in MCF-7 cells. 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-β-d -Gal p and 1, 3, 6-linked-β-d -Gal p residues, which was terminated with 1-linked-α-d -Glc p and 1-linked-α-l -Ara f terminal at O-3 position of 1, 3, 6-linked-β-d -Gal p 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 μg/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 μg/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.