Conjugated linoleic acid inhibits cell proliferation and ErbB3 signaling in HT-29 human colon cell line

被引:107
作者
Cho, HJ
Kim, WK
Kim, EJ
Jung, KC
Park, S
Lee, HS
Tyner, AL
Park, JHY
机构
[1] Hallym Univ, Div Life Sci, Chunchon 200702, South Korea
[2] Hallym Univ, Dept Pathol, Chunchon 200702, South Korea
[3] Dankook Univ, Dept Food Sci & Nutr, Seoul 140742, South Korea
[4] Sookmyung Womens Univ, Dept Sci Biol, Seoul 140742, South Korea
[5] Univ Illinois, Coll Med, Dept Mol Genet, Chicago, IL 60607 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2003年 / 284卷 / 06期
关键词
heregulin; phosphoinositide; 3-kinase; apoptosis;
D O I
10.1152/ajpgi.00347.2002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Conjugated linoleic acid (CLA) has chemoprotective properties in experimental cancer models, and in vitro studies have shown that CLA inhibits HT-29 colon cancer cell growth. ErbB2 and ErbB3 have been implicated in the development of colon cancer, and both proteins are expressed at high levels in the HT-29 cell line. Activation of ErbB2/ErbB3 heterodimers is regulated by the ErbB3 ligand heregulin. To examine CLA regulation of HT-29 cell proliferation and apoptosis and the influence of CLA on the ErbB3 signaling pathway, HT-29 cells were cultured in the presence of CLA and/or heregulin. CLA inhibited DNA synthesis and induced apoptosis of HT-29 cells. Although the addition of heregulin-alpha led to an increase in cell number, it was not able to counteract the negative growth regulatory effect of CLA. Immunoprecipitation/Western blot studies revealed that CLA inhibited heregulin-alpha-stimulated phosphorylation of ErbB2 and ErbB3, recruitment of the p85 subunit of phosphoinositide 3-kinase (PI3-kinase) to the ErbB3 receptor, ErbB3-associated PI3-kinase activities, and phosphorylation of Akt. CLA decreased ErbB2 and ErbB3 mRNA and protein levels in a dose-dependent manner. In conclusion, we demonstrate that CLA inhibits cell proliferation and stimulates apoptosis in HT-29 cells and that this may be mediated by its ability to downregulate ErbB3 signaling and the PI3-kinase/ Akt pathway.
引用
收藏
页码:G996 / G1005
页数:10
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