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Oncogenic ras alters sensitivity of mouse colonocytes to butyrate and fatty acid mediated growth arrest and apoptosis.
- Source :
-
Cancer letters [Cancer Lett] 2002 Dec 01; Vol. 186 (1), pp. 29-35. - Publication Year :
- 2002
-
Abstract
- 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 1mM butyrate decreased proliferation relative to LA or no PUFA treatment in both cell lines. At a higher butyrate dose (5mM), caspase 3 activity was elevated to a greater extent in Ras transformed cells. Only non-transformed cells were sensitive to the apoptogenic effects of DHA, indicating that Ras transformation alters sensitivity to dietary chemopreventive agents.
- Subjects :
- Animals
Cell Division drug effects
Colon cytology
DNA Adducts metabolism
Dose-Response Relationship, Drug
Fatty Acids, Omega-3
Fatty Acids, Unsaturated pharmacology
Mice
Triglycerides pharmacology
Apoptosis drug effects
Butyrates pharmacology
Colon drug effects
Docosahexaenoic Acids pharmacology
Genes, ras physiology
Linoleic Acid pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0304-3835
- Volume :
- 186
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cancer letters
- Publication Type :
- Academic Journal
- Accession number :
- 12183072
- Full Text :
- https://doi.org/10.1016/s0304-3835(02)00325-7