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Soybean
phytochemicals inhibit the growth of transplantable human prostate carcinoma and
tumor angiogenesis in mice
Jin-Rong Zhou, Eric T. Gugger, Toshihide
Tanaka, Yanping Guo, George L. Blackburn and Steven
K. Clinton
Nutrition/Metabolism Laboratory, Department of Surgery, Beth
Israel-Deaconess Medical Center, Harvard Medical School, Boston, MA 02215
[J.-R.Z., G.L.B.]; Archer Daniels Midland Company, Decatur, IL 62521 [E.T.G.,
Y.G.]; Department of Neurosurgery, Fuji City General Hospital, Fuji, Japan
[T.T.]; and The Arthur G. James Cancer Hospital and Research Institute, The Ohio
State University, Comprehensive Cancer Center, Columbus, OH 43210 [S.K.C.]. To whom correspondence and reprint requests should be
addressed: [J.-R.Z.].
The objectives of our studies are to characterize the ability of dietary soybean
components to inhibit the growth of prostate cancer in mice and alter tumor
biomarkers associated with angiogenesis.
Soy isoflavones (genistein or daidzein)
or soy phytochemical concentrate inhibit the growth of prostate cancer cells
LNCaP, DU 145 and PC-3 in vitro, but only at supraphysiologic concentrations,
i.e., 50% inhibitory concentration (IC(50)) > 50 micromol/L.
G2-M arrest and
DNA fragmentation consistent with apoptosis of prostate cancer cells are also
observed at concentrations causing growth inhibition.
In contrast, the in vitro
proliferation of vascular endothelial cells was inhibited by soy phytochemcials
at much lower concentrations.
We evaluated the ability of dietary soy
phytochemical concentrate and soy protein isolate to inhibit the growth of the
LNCaP human prostate cancer in severe combined immune-deficient mice.
Mice
inoculated subcutaneously with LNCaP cells (2 x 10(6)) were randomly assigned to
one of the six dietary groups based on the AIN-76A formulation for 3 wk.
A 2 x 3
factorial design was employed with two protein sources (20%, casein vs. soy
protein) and three levels of soy phytochemical concentrate (0, 0.2 and 1.0% of
the diet).
Soy components did not alter body weight gain or food intake.
Compared with casein-fed controls, the tumor volumes after 3 wk were reduced by
11% (P = 0.45) by soy protein, 19% (P = 0.17) by 0.2% soy phytochemical
concentrate, 28% by soy protein with 0.2% soy phytochemical concentrate (P <
0.05), 30% by 1.0% soy phytochemical concentrate (P < 0.05) and 40% by soy
protein with 1.0% soy phytochemical concentrate (P < 0.005).
Histologic
examination of tumor tissue showed that consumption of soy products
significantly reduced tumor cell proliferation, increased apoptosis and reduced
microvessel density.
The angiogenic protein insulin-like growth factor-I was
reduced in the circulation of mice fed soy protein and phytochemical
concentrate.
Our data suggest that dietary soy products may inhibit experimental
prostate tumor growth through a combination of direct effects on tumor cells and
indirect effects on tumor neovasculature.
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