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Antitumor activity of fucoidan against diffuse large B cell lymphoma <italic>in vitro</italic> and <italic>in vivo</italic>
Author(s) -
Guang Yang,
Qianqiao Zhang,
Yuanyuan Kong,
Bingqian Xie,
Minjie Gao,
Tao Yi,
Hongwei Xu,
Fenghuang Zhan,
Bojie Dai,
Jumei Shi,
Xiaosong Wu
Publication year - 2015
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmv094
Subject(s) - fucoidan , in vivo , pharmacology , apoptosis , cell growth , cancer research , chemistry , biology , biochemistry , polysaccharide , microbiology and biotechnology
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.

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