A novel polysaccharide from Sargassum integerrimum induces apoptosis in A549 cells and prevents angiogensis in vitro and in vivo

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作者
Ge Liu
Shan Kuang
Shimei Wu
Weihua Jin
Chaomin Sun
机构
[1] Key Laboratory of Experimental Marine Biology,
[2] Institute of Oceanology,undefined
[3] Chinese Academy of Sciences,undefined
[4] Laboratory for Marine Biology and Biotechnology,undefined
[5] Qingdao National Laboratory for Marine Science and Technology,undefined
[6] College of Earth Science,undefined
[7] University of Chinese Academy of Sciences,undefined
[8] Key Laboratory of Biobased Materials,undefined
[9] Qingdao Institute of Bioenergy and Bioprocess Technology,undefined
[10] Chinese Academy of Sciences,undefined
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Scientific Reports | / 6卷
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摘要
Many polysaccharides isolated from plants have exhibited promising antitumor activities. The aim of this study is to investigate the antitumor activity of the novel polysaccharide named SPS from Sargassum integerrimum, elucidate the underlying anticancer mechanism in a human lung cancer cell line A549 and evaluate its anti-angiogenic activity both in vitro and in vivo. The results show that SPS significantly reduces A549 cells viability in a dose- and time-dependent manner via MTT method. Flow cytometry analysis indicates that SPS could induce cell apoptosis, the loss of mitochondrial membrane potential (MMP), generation of reactive oxygen species (ROS) and G2/M phase cell cycle arrest of A549 cells. Up-regulation of the expressions of P53 and Bax, down-regulation of the expression of Bcl-2 and activation of cleaved caspase-3, caspase-9 and PARP are also detected by western blotting after the treatment of SPS. In addition, SPS inhibits the proliferation, migration and cord formation of human umbilical vein endothelial cells (HUVECs) in vitro and prevents the vascular development of zebrafish embryos in vivo. Altogether, our data prove the anticancer and anti-angiogenesis properties of SPS and provide further insights into the potential pharmacological application of SPS as antitumor and anti-angiogenic agent against lung cancer.
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