Effects of dietary menhaden oil, soy, and a cyclooxygenase inhibitor on human breast cancer cell growth and metastasis in nude mice

JM Connolly, XH Liu, DP Rose - 1997 - Taylor & Francis
JM Connolly, XH Liu, DP Rose
1997Taylor & Francis
The purpose of Study 1 was to examine the effect of dietary soy on the progression of MDA‐
MB‐435 human breast cancer cell solid tumors in nude mice. When toasted soy chips were
fed at levels of 5%, 10%, or 20%(wt/wt) in a high‐fat, linoleic acid‐rich diet for 12 weeks,
there was a trend for larger mammary fat pad tumors to occur with increasing soy intake.
However, compared with the controls the severity of macroscopic lung metastasis was
reduced significantly in the groups fed 10% and 20% soy. Study 2 compared the effects of …
Abstract
The purpose of Study 1 was to examine the effect of dietary soy on the progression of MDA‐MB‐435 human breast cancer cell solid tumors in nude mice. When toasted soy chips were fed at levels of 5%, 10%, or 20% (wt/wt) in a high‐fat, linoleic acid‐rich diet for 12 weeks, there was a trend for larger mammary fat pad tumors to occur with increasing soy intake. However, compared with the controls the severity of macroscopic lung metastasis was reduced significantly in the groups fed 10% and 20% soy. Study 2 compared the effects of diets containing 23% corn oil (CO), 18% menhaden oil (MO) + 5% CO, 18% MO + 5% CO + 10% soy chips, and MO or soy‐supplemented diets + in‐domethacin treatment in the same animal model. Feeding the 18% MO diet without soy or indomethacin reduced primary tumor growth; statistically significant effects were not observed in any of the other groups. All three of the groups with MO supplementation showed a reduction in the occurrence and severity of macroscopic lung metastases, together with the expected decreases in tumor prostaglandin ? levels. These effects were most pronounced when MO was combined with indomethacin treatment. When indomethacin was given with dietary soy, the previously reported suppressive effect of the cyclooxygenase inhibitor on MDA‐MB‐435 cell tumor progression was lost, despite reductions in tumor prostaglandin ? concentrations.
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