| Literature DB >> 26358321 |
Guang Yang1, Qianqiao Zhang1, Yuanyuan Kong1, Bingqian Xie1, Minjie Gao1, Yi Tao1, Hongwei Xu2, Fenghuang Zhan2, Bojie Dai3, Jumei Shi4, Xiaosong Wu4.
Abstract
Fucoidan is one of the major sulfated polysaccharides isolated from brown seaweeds. In this study, we determined the anti-cancer activity of fucoidan on diffuse large B cell lymphoma (DLBCL) cells both in vitro and in vivo. Fucoidan inhibited the growth of DLBCL cells in a dose- and time-dependent manner, and fucoidan treatment provoked G0/G1 cell cycle arrest, which was accompanied by p21 up-regulation and cyclin D1, Cdk4, and Cdk6 down-regulation. Fucoidan also induced caspase-dependent cell apoptosis in DLBCL cell lines and primary DLBCL cell. In addition, fucoidan treatment caused the loss of mitochondrial membrane potential and the release of cytochrome c and apoptosis-inducing factor from the mitochondria into the cytosol. Fucoidan also potentiated the activities of carfilzomib in killing DLBCL cells. Oral administration of fucoidan effectively inhibited tumor growth in xenograft mouse models. Our findings reveal the novel function of fucoidan as an anti-DLBCL agent, which can be used in the clinical treatment of DLBCL.Entities:
Keywords: apoptosis; cell cycle; diffuse large B cell lymphoma; fucoidan
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Year: 2015 PMID: 26358321 DOI: 10.1093/abbs/gmv094
Source DB: PubMed Journal: Acta Biochim Biophys Sin (Shanghai) ISSN: 1672-9145 Impact factor: 3.848