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Old 12-04-2005, 08:11 AM   #1
CLTann
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Join Date: Oct 2005
Posts: 476
question on soy, phytoestrogen, grapefruit.

soy extract has been known to be antigonistic to Tamoxifen, or to Arimidex. So are other phytoestrogen containing seeds. Grapefruit should be avoided to go with many medicines, because the enzyme from grapefruit will interfere with most medicines in liver. Just a note of caution.

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Old 12-04-2005, 05:34 PM   #2
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effects of dietary flaxseed on tumor biological markers and urinary lignan excretion

To add to the debate.

Here is the summary of the trial from the NCBI web site. It is a pay for view so I have not had access to the full trial.

It looks like the results were based on tumour tissue analysis of real human patients and not poor mice for a change.



http://www.ncbi.nlm.nih.gov/entrez/...t_uids=15897583

1: Clin Cancer Res. 2005 May 15;11(10):3828-35. Related Articles, Books, LinkOut
Click here to read
Dietary flaxseed alters tumor biological markers in postmenopausal breast cancer.

Thompson LU, Chen JM, Li T, Strasser-Weippl K, Goss PE.

Department of Nutritional Sciences, Princess Margaret Hospital, University of Toronto, Toronto, Ontario, Canada.

PURPOSE: Flaxseed, the richest source of mammalian lignan precursors, has previously been shown to reduce the growth of tumors in rats. This study examined, in a randomized double-blind placebo-controlled clinical trial, the effects of dietary flaxseed on tumor biological markers and urinary lignan excretion in postmenopausal patients with newly diagnosed breast cancer. EXPERIMENTAL DESIGN: Patients were randomized to daily intake of either a 25 g flaxseed-containing muffin (n = 19) or a control (placebo) muffin (n = 13). At the time of diagnosis and again at definitive surgery, tumor tissue was analyzed for the rate of tumor cell proliferation (Ki-67 labeling index, primary end point), apoptosis, c-erbB2 expression, and estrogen and progesterone receptor levels. Twenty-four-hour urine samples were analyzed for lignans, and 3-day diet records were evaluated for macronutrient and caloric intake. Mean treatment times were 39 and 32 days in the placebo and flaxseed groups, respectively. RESULTS: Reductions in Ki-67 labeling index (34.2%; P = 0.001) and in c-erbB2 expression (71.0%; P = 0.003) and an increase in apoptosis (30.7%; P = 0.007) were observed in the flaxseed, but not in the placebo group. No significant differences in caloric and macronutrient intake were seen between groups and between pre- and posttreatment periods. A significant increase in mean urinary lignan excretion was observed in the flaxseed group (1,300%; P < 0.01) compared with placebo controls. The total intake of flaxseed was correlated with changes in c-erbB2 score (r = -0.373; P = 0.036) and apoptotic index (r = 0.495; P < 0.004). CONCLUSION: Dietary flaxseed has the potential to reduce tumor growth in patients with breast cancer.

Publication Types:

* Clinical Trial
* Randomized Controlled Trial


PMID: 15897583 [PubMed - indexed for MEDLINE]


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