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Inactivation of NF-κB by genistein is mediated via Akt signaling pathway in breast cancer cells

Oncogene volume 22, pages 4702–4709 (2003)Cite this article

Abstract

Genistein, a natural isoflavonoid found in soybean products, has been proposed to be associated with a lower rate of breast cancer in Asian women. Studies from our laboratory and others have shown that genistein can induce apoptosis by regulating the expression of apoptosis-related genes in breast cancer cells. However, the precise molecular mechanism(s) by which genistein induces apoptotic cell death is not clear. In order to investigate such mechanism, we tested the role of Akt and NF-κB in genistein-treated MDA-MB-231 breast cancer cells. We found that inhibition of cell growth and induction of apoptosis by genistein are partly mediated through the downregulation of Akt and NF-κB pathways. Gel shift assay showed that NF-κB DNA-binding activity in MDA-MB-231 cells transfected with Akt cDNA was induced, suggesting that there is a cross-talk between NF-κB and Akt signaling pathway. Moreover, we found that genistein could abrogate EGF and Akt induced NF-κB activation. From these results, we conclude that the inactivation of NF-κB by genistein in MDA-MB-231 breast cancer cells is partly mediated via Akt pathway, which could be useful for rational design of strategies for the prevention and/or treatment of breast cancer.

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Acknowledgements

This work was partly funded by a grant from the National Cancer Institute, NIH (CA83695-O1A2 awarded to FHS) and was also supported by an unrestricted grant from the RGK foundation.

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  1. Department of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA

    Lijie Gong, Yiwei Li, Ana Nedeljkovic-Kurepa & Fazlul H Sarkar

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  1. Lijie Gong
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  2. Yiwei Li
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  3. Ana Nedeljkovic-Kurepa
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  4. Fazlul H Sarkar
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Correspondence to Fazlul H Sarkar.

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Gong, L., Li, Y., Nedeljkovic-Kurepa, A. et al. Inactivation of NF-κB by genistein is mediated via Akt signaling pathway in breast cancer cells. Oncogene 22, 4702–4709 (2003). https://doi.org/10.1038/sj.onc.1206583

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