Oncogenic ras alters sensitivity of mouse colonocytes to butyrate and fatty acid mediated growth arrest and apoptosis

被引:12
作者
Turner, ND
Zhang, JH
Davidson, LA
Lupton, JR
Chapkin, RS
机构
[1] Texas A&M Univ, Fac Nutr, College Stn, TX 77843 USA
[2] Texas A&M Univ, Ctr Environm & Rural Hlth, College Stn, TX 77843 USA
关键词
colon cancers butyrate; linoleic acid; docosahexaenoic acid; proliferation; apoptosis; ras;
D O I
10.1016/S0304-3835(02)00325-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Docosahexaenoic acid (DHA) and butyrate favorably modulate colonocyte proliferation and apoptosis. In order to elucidate how oncogenic Ras modulates responses to these chemopreventive nutrients, we incubated isogenic non-transformed and Ras malignant transformed mouse colon cells with butyrate and DHA or linoleic acid (LA). Combining DHA with 1 mM butyrate decreased proliferation relative to LA or no PUFA treatment in both cell lines. At a higher butyrate dose (5 mM), caspase 3 activity was elevated to a greater extent in Ras transformed cells. Only non-transformed cells were sensitive to the a poptogenic effects of DHA, indicating that Ras transformation alters sensitivity to dietary chemopreventive agents. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:29 / 35
页数:7
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