Butyrate and propionate downregulate ERK phosphorylation in HT-29 colon carcinoma cells prior to differentiation

被引:22
作者
Davido, DJ
Richter, F
Boxberger, F
Stahl, A
Menzel, T
Lührs, H
Löffler, S
Dusel, G
Rapp, UR
Scheppach, W
机构
[1] Univ Wurzburg, Med Klin, D-97080 Wurzburg, Germany
[2] Univ Wurzburg, Inst Med Strahlenkunde & Zellforsch, D-97078 Wurzburg, Germany
关键词
adenocarcinoma; butyrate; extracellular signal-regulated kinases; HT-29; cells; propionate; short-chain fatty acids;
D O I
10.1097/00008469-200108000-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have characterized the effects of different short-chain fatty acids (SCFAs) on cell growth and differentiation as well as the phosphorylation state of ERK1 and 2 in the human colon adenocarcinoma cell line HT-29. Of the five SCFAs tested, only butyrate and propionate impaired cellular proliferation. Moreover, butyrate and propionate specifically resulted in a decrease in ERK1 and 2 phosphorylation at 3 and 6 hours post-treatment, suggesting a correlation between the ability of these SCFAs to inhibit cellular proliferation and decrease ERK phosphorylation. Notably, the decrease in ERK phosphorylation was observed prior to the induction of the differentiation markers alkaline phosphatase (AP) and carcinoembryonic antigen (CEA) by butyrate and propionate from days 6 to 18 post-treatment. In the case of butyrate- and propionate-induced differentiation, ERK phosphorylation is a marker and may play a role in the proliferation and/or differentiation states of this cell line. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:313 / 321
页数:9
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