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Carcinogenesis Advance Access published online on August 19, 2005

Carcinogenesis, doi:10.1093/carcin/bgi214
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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 11, 2005
Revised July 7, 2005
Accepted August 12, 2005

MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Inhibition of Akt signaling and enhanced ERK1/2 activity are involved in induction of macroautophagy by triterpenoid B-group soyasaponins in colon cancer cells

Allison A. Ellington 1, Mark A. Berhow 2, and Keith W. Singletary 1*

1 Department of Food Science and Human Nutrition, 905 South Goodwin Ave, Bevier Hall, Urbana, IL, 61801
2 National Center for Agricultural Research Service, Peoria, IL, 61601

* To whom correspondence should be addressed.
Keith W. Singletary, E-mail: kws{at}uiuc.edu


   Abstract

Triterpenoid B-group soyasaponins have been found to induce macroautophagy in human colon cancer cells at concentrations obtainable through consumption of legume foodstuffs. In the present studies the mechanism(s) for this autophagy-inducing action of soyasaponins was evaluated by measuring changes in signal transduction pathways associated with autophagy. Specifically, inhibition of the Akt signaling pathway and enhanced activity of ERK1/2 have previously been implicated in controlling induction of macroautophagy in mammalian cancer cells. Here we show that these pathways are also involved in B-group soyasaponin-induced macroautophagy, as changes in enzyme activities preceded significant increases in autophagic activity. The autophagic capacity of HCT-15 cells was significantly increased by six hours post-saponin exposure, which led us to measure alterations in signaling events that preceded this time point. We determined that exposure to B-group soyasaponins suppressed Akt activity maximally by 50%, which was associated with a reduction in the activating phosphorylation of the Akt-serine473 residue. In addition, ERK1/2 activity was significantly increased by 60%, and was determined to be necessary for B-group soyasaponin-induced autophagy. The raf-1 kinase has been identified as a potential point of cross-talk between the Akt and ERK1/2 signaling cascades. Following B-group soyasaponin treatment activity of raf-1 was significantly increased by a maximal 200%, suggesting that this enzyme in part modulates the enhanced ERK1/2 activity. These results provide new insights into the signaling events that control induction of autophagy by B-group soyasaponins in human colon cancer cells and suggest that soyasaponins warrant further study as potential colon cancer chemopreventive agents.

Keywords: colon cancer; soyasaponins; macroautophagy; Akt; ERK1/2.
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