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Effects of carboxymethyl chitosan oligosaccharide on regulating immunologic function and inhibiting tumor growth.
Jiang, Zhiwen; Wang, Shuning; Hou, Jun; Chi, Jinhua; Wang, Shuo; Shao, Kai; Liu, Wanshun; Sun, Rongju; Han, Baoqin.
Afiliação
  • Jiang Z; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China; Laboratory for Marine Drugs and Bioproducts of Pilot National Laboratory for Marine Science and Technology, Qingdao, 266235, PR China.
  • Wang S; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China.
  • Hou J; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China.
  • Chi J; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China.
  • Wang S; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China.
  • Shao K; Department of Central Laboratory, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, PR China.
  • Liu W; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China.
  • Sun R; Department of Emergency, General Hospital of PLA, Beijing, 100853, PR China. Electronic address: srj20170101@163.com.
  • Han B; Laboratory of Biochemistry and Biomedical Materials, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, PR China; Laboratory for Marine Drugs and Bioproducts of Pilot National Laboratory for Marine Science and Technology, Qingdao, 266235, PR China. Electronic address: baoqi
Carbohydr Polym ; 250: 116994, 2020 Dec 15.
Article em En | MEDLINE | ID: mdl-33049904
ABSTRACT
Herein, the effects of carboxymethyl chitosan oligosaccharide (CM-COS) on regulating immunologic function and inhibiting hepatocellular tumor growth were evaluated. Results showed that CM-COS caused dramatic viability loss of hepatocellular carcinoma BEL-7402 with non-toxicity towards normal liver L-02 cells. CM-COS repressed tumor growth of hepatoma-22, and elevated the spleen index and thymus index of tumor-bearing mice. Contents of VEGF and MMP-9 were significantly down-regulated by CM-COS. Histological analyses revealed that CM-COS promoted tumor cell necrosis and produced no significant toxicity to spleen tissues. Moreover, expressions of Caspase-3 in tumor tissues and IL-2 in spleen tissues were significantly activated by CM-COS. Additionally, in vitro cell viability, phagocytic capability and NO production of mouse peritoneal macrophages exposed to CM-COS were significantly higher. CM-COS remarkably increased the in vivo phagocytosing capacity of peritoneal macrophages of Kunming mice. Taken together, our findings suggested that CM-COS might be potentially effective and non-toxic candidate as anti-hepatoma agents.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Macrófagos Peritoneais / Carcinoma Hepatocelular / Quitosana / Fígado / Neoplasias Hepáticas Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Macrófagos Peritoneais / Carcinoma Hepatocelular / Quitosana / Fígado / Neoplasias Hepáticas Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article