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Carcinogenesis Advance Access published online on September 30, 2005

Carcinogenesis, doi:10.1093/carcin/bgi230
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© The Author 2005. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oupjournals.org
Received May 5, 2005
Revised September 8, 2005
Accepted September 17, 2005

MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Inhibition of growth factor-induced ras signaling in vascular endothelial cells and angiogenesis by 3,3'-diindolylmethane

Xiaofei Chang 1, Gary L. Firestone 2, and Leonard F. Bjeldanes 1*

1 Department of Nutritional Sciences and Toxicology, University of California, Berkeley, CA 94720, USA
2 Department of Molecular Cell Biology, University of California, Berkeley, California 94720, USA

* To whom correspondence should be addressed.
Leonard F. Bjeldanes, E-mail: lfb{at}nature.berkeley.edu


   Abstract

3,3'-Diindolylmethane (DIM), an indole derivative produced on consumption of broccoli and other cruciferous vegetables, has been shown to have multiple anti-cancer effects in both in vivo and in vitro models. The present study was carried out to clarify the mechanism of DIM's antiangiogenic activity. We found that DIM can inhibit vascular endothelial growth factor (VEGF)-induced cell proliferation and DNA synthesis in human umbilical vascular endothelial cells (HUVECs). Consistent with this inhibition, VEGF-induced extracellular signal-regulated kinase (ERK1/2) phosphorylation was greatly reduced. However, VEGF receptor phosphorylation induced by VEGF was not affected by DIM, indicating that DIM does not exert a direct and specific effect on this receptor tyrosine kinase activity. Further studies showed that DIM had a similar inhibitory effect on ERK1/2 phosphorylation induced by a variety of growth factors. Furthermore, Ras-GTP content, which dramatically increased after HUVECs were challenged by either individual growth factors or serum, was reduced by nearly 80% with 25 µM DIM treatment, which in turn resulted in the reduced activities of Raf and MEK, culminating in the drop of ERK1/2 activation. Over expression of constitutively active GTPase mutant, Ras G12V, in HUVECs reversed the inhibitory effect of DIM on ERK1/2 activation. In a rodent Matrigel plug model, the presence of DIM strongly reduced VEGF-induced neovascularization, indicating that DIM is active in vivo. These data provide evidence that DIM inhibits Ras signaling induced by VEGF and other growth factors, which interferes with its downstream biological effects necessary for angiogenesis.

Keywords: 3,3'-Diindolylmethane; VEGF; Ras; MAPK/ERK; angiogenesis.
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