Yulangsan polysaccharide inhibits 4T1 breast cancer cell proliferation and induces apoptosis in vitro and in vivo

细胞凋亡 乳腺癌 血管生成 体内 癌症研究 癌症 转移 活力测定 细胞生长 流式细胞术 癌细胞 标记法 生物 医学 药理学 免疫学 内科学 生物化学 生物技术
作者
Qin Ni,Shiyin Lu,Ning Chen,Chunxia Chen,Qiuqiao Xie,Xiaojie Wei,Fangxing Ye,Junhui He,Yuchun Li,Lixiu Chen,Luhui Jiang,Xiaoqi Lu,Yuchan Yuan,Jian Li,Yang Jiao,Renbin Huang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:121: 971-980 被引量:26
标识
DOI:10.1016/j.ijbiomac.2018.10.082
摘要

Yulangsan polysaccharide (YLSPS) is derived from the root of Millettia pulchra (Benth.) Kurz var. Recent studies have postulated YLSPS as a regimen for cancer treatment. However, the underlying mechanism anti-breast cancer is still poorly unknown. The aim of this study was to examine the suppressive and apoptosis effect of YLSPS on the growth of breast cancer cell 4T1 and its possible underlying mechanism. In this study, breast cancer cell 4T1 viability and apoptosis were assessed by CCK-8 and flow cytometry, relative quantitative real-time PCR and western blot after treated with drug-serum of YLSPS. Furthermore, therapy experiments were conducted using a Balb/c mouse transplanted tumor model of breast cancer. The number of apoptotic cells and microvascular density (MVD) in the tumor tissues were assessed by TUNEL and CD34 immunostaining. Immunohistochemical assays and ELISA were used to detect the expression of VEGF, Bcl-2, Bax and Caspase-3 in the tissues. The in vitro studies showed that the drug-serum of YLSPS significantly inhibition of proliferation and effectively induced apoptosis of 4T1 cells. Oral administration of YLSPS in the breast cancer models significantly reduced the tumor volume and weight. The enhanced antitumor efficacy was associated with decreased angiogenesis, an enhanced antioxidant capacity, an increased induction of apoptosis and an inhibition of lung metastasis. These findings indicate that YLSPS significantly inhibited mouse breast cancer growth in vitro and in vivo. These data suggest that YLSPS may serve as a potential therapeutic agent for breast cancer.
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