Search PubMedSearch

PubMed · 8729142

n-3 fatty acids decrease colonic epithelial cell proliferation in high-risk bowel mucosa.

Abstract

The n-3 fatty acids (C20:5, eicosapentaenoic acid; c22:6, docosahexaenoic acid) may be important in the development, growth, and metastasis of colon cancer, a leading cause of death in North America. Patients who have had a bowel neoplasm have a high risk of developing a second neoplasm, and this risk is associated with a high percentage of cells correspond to the S phase of bromodeoxyuridine (BrdUrd) labeling in mucosal epithelial cells. To determine the effect of n-3 fatty acid supplementation on DNA synthesis of rectal mucosa, patients with stage 1 or stage 2 colon carcinoma or adenomatous polyps were randomized to consume either 9 g/d n-3 fatty acid capsules or 9 g/d placebo capsules. Plasma phospholipid fatty acid analysis and proctoscopic mucosal biopsies were performed at baseline, 3, and 6 mon. Colonic crypts were isolated from the mucosa, disassociated with enzymes, and incubated with BrdUrd, and %S phase was measured by flow cytometry. The plasma phospholipid n-6/n-3 ratio was determined by gas chromatography. Supplement compliance was assessed by plasma phospholipid n-6/n-3 ratio. Mean capsule consumption in these two group was 82%. Prior to supplementation, there were no significant differences in the %S phase and the plasma n-6/n-3 ratio between these groups. Patients whose colonic epithelial cells indicated hyperproliferation at baseline showed a strongly positive correlation to the %S phase of BrdUrd uptake and the n-6/n-3 ratio. There was no significant change after n-3 treatment in patients with low baseline. Those in the placebo group showed no significant difference in n-6/n-3 ratio, although there was an increase in the %S phase of BrdUrd uptake at 6 mon. The n-3 group did not have significant side effects, and polyps were not found after completing 12 mon of n-3 fatty acid supplementation. This study suggests that n-3 fatty acid may be a useful chemopreventive agent in some patients as reflected in a plasma biomarker of colon tumor growth and metastasis. A low plasma phospholipid n-6/n-3 fatty acid ratio may serve as a nutritional marker that is associated with colonic epithelial cell hyperproliferation in the n-3-supplemented group as compared with the placebo group. Characteristics of mucosal proliferation at baseline may be a crucial factor for the effect of n-3 fatty acid supplementation.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Y C Huang, J M Jessup, R A Forse, S Flickner, D Pleskow, H T Anastopoulos, V Ritter, G L Blackburn. 1996. n-3 fatty acids decrease colonic epithelial cell proliferation in high-risk bowel mucosa.. https://doi.org/10.1007/bf02637099

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Regulation of cell division and the cytoskeleton by mitogen-activated protein kinases in higher plants.

The microtubule-associated protein 2 kinase (MAP2-kinase), now better known as mitogen-activated protein kinase (MAPK), was initially discovered in association with the cytoskeleton, and was later also implicated in cell division. The importance of mitogenic stimulation in plant development roused interest in finding the plant homologues of MAPKs. However, data on plant MAPKs in cell division are rather sparse and fragmentary. Therefore we place the available information on cell cycle control of MAPKs in plants into a broader context. We discuss four aspects of cell division control: cell proliferation and the G1/S-phase transition, G2-phase and mitosis, cytokinesis, and cytoskeletal reorganisation. Future work will reveal to what extent plants use signalling pathways that are similar or different to those of animal or yeast cells in regulating cell divisions.

Cell Division

Phosphorylation and regulation of Raf by Akt (protein kinase B).

Activation of the protein kinase Raf can lead to opposing cellular responses such as proliferation, growth arrest, apoptosis, or differentiation. Akt (protein kinase B), a member of a different signaling pathway that also regulates these responses, interacted with Raf and phosphorylated this protein at a highly conserved serine residue in its regulatory domain in vivo. This phosphorylation of Raf by Akt inhibited activation of the Raf-MEK-ERK signaling pathway and shifted the cellular response in a human breast cancer cell line from cell cycle arrest to proliferation. These observations provide a molecular basis for cross talk between two signaling pathways at the level of Raf and Akt.

Cell Division