Exopolysaccharide of Antarctic bacterium Pseudoaltermonas sp S-5 induces apoptosis in K562 cells

被引:25
|
作者
Chen, Guochuang [2 ,3 ]
Qian, Wen [1 ,5 ]
Li, Jing [1 ]
Xu, Yanghui [1 ]
Chen, Kaoshan [1 ,2 ,3 ,4 ]
机构
[1] Wannan Med Coll, Dept Pharm, Anhui Prov Key Lab Act Biol Macromol, Anhui Prov Engn Res Ctr Polysaccharide Drugs, Wuhu 241000, Peoples R China
[2] Shandong Univ, Sch Life Sci, Jinan 250100, Peoples R China
[3] Shandong Univ, Natl Glycoengn Res Ctr, Jinan 250100, Peoples R China
[4] Shandong Univ, State Key Lab Microbial Technol, Jinan 250100, Peoples R China
[5] Huaibei Peoples Hosp, Dept Pharm, Huaibei 235000, Peoples R China
关键词
Antarctic bacterium; Exopolysaccharide; Apoptosis; Intrinsic pathway; Human leukemia; K562; cells; BCL-2; FAMILY-MEMBERS; CANCER DEVELOPMENT; BETA-GLUCAN; POLYSACCHARIDE; MITOCHONDRIA; PROTEIN; ACTIVATION; ARREST; DEATH;
D O I
10.1016/j.carbpol.2014.12.045
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this study was to investigate the anticancer activity of exopolysaccharide (PEP) of Antarctic bacterium Pseudoaltermonas sp. S-5 and elucidate the underlying molecular mechanisms. PEP significantly inhibited the growth of human leukemia K562 cells. Results of morphological characterization showed that PEP-treated cells displayed typical morphological characteristics of apoptosis such as condensation of chromatin and formation of apoptotic bodies. Flow cytometry analyses and colorimetric assay demonstrated that PEP induced collapse of mitochondrial membrane potential and activation of caspase-9, which indicated that intrinsic apoptotic signaling pathway was involved in apoptosis induced by PEP in K562 cells. Western blot analysis showed that PEP increased the ratio of Bax/Bcl-2. In addition, calcium signal might contribute to the cytotoxicity of PEP against K562 cells. These findings suggest that PEP may be potentially effective drug against human leukemia. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:107 / 114
页数:8
相关论文
共 50 条
  • [41] Polylysine induces changes in the membrane electrical properties of K562 cells
    Santini, MT
    Cametti, C
    Morelli, G
    Indovina, PL
    PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1996, 65 : PH533 - PH533
  • [42] Geldanamycin induces cell cycle arrest in K562 erythroleukemic cells
    Kim, HR
    Lee, CH
    Choi, YH
    Kang, HS
    Kim, HD
    IUBMB LIFE, 1999, 48 (04) : 425 - 428
  • [43] Effects of Rehmannia glutinosa polysaccharides on the proliferation and apoptosis of K562 cells
    Fan, Qilan
    Li, Jialin
    Xu, Chunjuan
    Wu, Suzhen
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2020, 33 (04) : 1555 - 1560
  • [44] Prevention of homoharringtonine induced apoptosis by antioxidanis in K562 cells.
    Mai, Wenyuan
    Lin, Maofang
    Jin, Jie
    BLOOD, 2006, 108 (11) : 172B - 172B
  • [45] A potent natural inhibitor of proliferating and inducer of apoptosis on K562 cells
    Niu, YP
    CLINICAL IMMUNOLOGY, 2005, 115 : S261 - S261
  • [46] Berbamine-induced apoptosis in human leukemia K562 cells
    Zhao, XY
    Xu, L
    Wu, D
    Xu, RZ
    BLOOD, 2004, 104 (11) : 144B - 144B
  • [47] Induction of apoptosis in human leukemia K562 cells by cardiotoxin III
    Yang, SH
    Lu, MC
    Chien, CM
    Tsai, CH
    Lu, YJ
    Hour, TC
    Lin, SR
    LIFE SCIENCES, 2005, 76 (21) : 2513 - 2522
  • [48] Effects of antioxidants on apoptosis induced by dasatinib and nilotinib in K562 cells
    Damiano, Sara
    Montagnaro, Serena
    Puzio, Maria V.
    Severino, Lorella
    Pagnini, Ugo
    Barbarino, Marcella
    Cesari, Daniele
    Giordano, Antonio
    Florio, Salvatore
    Ciarcia, Roberto
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2018, 119 (06) : 4845 - 4854
  • [49] Elemene induces apoptosis and regulates expression of bcl-2 protein in human leukemia K562 ceLls
    袁静
    顾振纶
    周文轩
    郭次仪
    ActaPharmacologicaSinica, 1999, (02) : 8 - 11
  • [50] Elemene induces apoptosis and regulates expression of bcl-2 protein in human leukemia K562 cells
    Yuan, J
    Gu, ZL
    Chou, WH
    Kwok, CY
    ACTA PHARMACOLOGICA SINICA, 1999, 20 (02) : 103 - 106