A glycoprotein from Laminaria japonica induces apoptosis in HT-29 colon cancer cells

被引:62
|
作者
Go, Hiroe [1 ]
Hwang, Hye-Jung [1 ]
Nam, Taek-Jeong [1 ]
机构
[1] Pukyong Natl Univ, Dept Food Sci & Biotechnol, Pusan 608737, South Korea
关键词
Seaweed; Glycoprotein; Laminaria japonica; Apoptosis; Cell cycle arrest; INDUCED LIVER-INJURY; PORPHYRA-YEZOENSIS; CYCLE ARREST; DEATH DOMAIN; IN-VITRO; POLYSACCHARIDE; FUCOIDAN; PATHWAY; SEAWEEDS; PROTEIN;
D O I
10.1016/j.tiv.2010.06.018
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
We isolated a novel glycoprotein from the brown alga Laminaria japonica that has antiproliferative effects on HT-29 colon cancer cells. We also identified the mechanism by which this glycoprotein, named LJGP, induces apoptosis. MTS assays showed that LJGP inhibited the proliferation of several cancer cell lines (AGS, HepG2, HT-29) in a dose-dependent manner. Especially in HT-29 cells, proliferation was significantly decreased. LJGP treatment on HT-29 displayed several apoptotic features, such as DNA fragmentation, sub-G1 arrest, caspase-3 activation, and PARP degradation. Consistent with sub-G1 arrest. LJGP decreased the expression of Cdk2, cyclin E, cyclin D1, PCNA, E2F-1, and phosphorylated pRb. Furthermore, the increase of p27 expression was observed. We also determined that LJGP-induced apoptosis leads to the formation of a death-induced signaling complex of Fas, FADD, and procaspase-8. LJGP induced the reduction of mitochondrial membrane potential with activation of the Bcl-2 family of proteins and caspase-9. These findings suggest that LJGP inhibits HT-29 cell proliferation by inducing apoptosis, which may be mediated via multiple pathways, including the Fas signaling pathway, the mitochondrial pathway, and cell cycle arrest. Therefore, LJGP can be a useful treatment option for colon cancer in humans. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1546 / 1553
页数:8
相关论文
共 50 条
  • [1] A Glycoprotein from Laminaria japonica Induces Cell Cycle Arrest and Apoptosis in HT-29 Colon Cancer Cells.
    Go, H.
    Kim, I. H.
    Hwang, H. J.
    Nam, T. J.
    [J]. ENDOCRINE REVIEWS, 2010, 31 (03)
  • [2] Polyethylene glycol induces apoptosis in HT-29 cells: Mechanism for chemoprevention of colon cancer
    Roy, HK
    Dibaise, JK
    Ansari, S
    Black, JB
    Karolski, WJ
    [J]. GASTROENTEROLOGY, 2001, 120 (05) : A615 - A616
  • [3] Induction of apoptosis by puerarin in colon cancer HT-29 cells
    Yu, Zengli
    Li, Wenjie
    [J]. CANCER LETTERS, 2006, 238 (01) : 53 - 60
  • [4] Induction of apoptosis in HT-29 colon cancer cells by phloretin
    Park, So Young
    Kim, Eun Ji
    Shin, Hyun-Kyung
    Kwon, Dae Young
    Kim, Myung Sunny
    Surh, Young-Joon
    Park, Jung Han Yoon
    [J]. JOURNAL OF MEDICINAL FOOD, 2007, 10 (04) : 581 - 586
  • [5] Polyethylene glycol induces apoptosis in HT-29 cells: potential mechanism for chemoprevention of colon cancer
    Roy, HK
    DiBaise, JK
    Black, J
    Karolski, WJ
    Ratashak, A
    Ansari, S
    [J]. FEBS LETTERS, 2001, 496 (2-3) : 143 - 146
  • [6] Arachidonic acid induces ER stress and apoptosis in HT-29 human colon cancer cells
    Bae, Sijeong
    Kim, Min-Kyoung
    Kim, Hong Seok
    Moon, Young-Ah
    [J]. ANIMAL CELLS AND SYSTEMS, 2020, 24 (05) : 260 - 266
  • [7] Kaempferol induces cell cycle arrest and apoptosis in HT-29 human colon cancer cells
    Cho, HJ
    Kwon, GT
    Park, JHY
    [J]. FASEB JOURNAL, 2005, 19 (05): : A1694 - A1694
  • [8] Phloroglucinol induces apoptosis via apoptotic signaling pathways in HT-29 colon cancer cells
    Kang, Mi-Hye
    Kim, In-Hye
    Nam, Taek-Jeong
    [J]. ONCOLOGY REPORTS, 2014, 32 (04) : 1341 - 1346
  • [9] Kimchi markedly induces apoptosis in HT-29 human colon carcinoma cells
    Yu, Ting
    Park, Eui-Seong
    Song, Gil-Hoon
    Zhao, Xin
    Yi, Ruo-Kun
    Park, Kun-Young
    [J]. JOURNAL OF FOOD BIOCHEMISTRY, 2021, 45 (01)
  • [10] Induction of apoptosis by phloretin in HT-29 human colon cancer cells
    Park, SY
    Kim, EJ
    Shin, HK
    Kwon, DY
    Surh, YJ
    Park, JHY
    [J]. FASEB JOURNAL, 2006, 20 (04): : A568 - A568