Volume 123, Issue 7 pp. 1508-1515
Carcinogenesis

Inhibition of epidermal growth factor receptor signaling pathway by delphinidin, an anthocyanidin in pigmented fruits and vegetables

Farrukh Afaq

Farrukh Afaq

Department of Dermatology, University of Wisconsin, Madison, WI

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Najia Zaman

Najia Zaman

Department of Dermatology, University of Wisconsin, Madison, WI

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Naghma Khan

Naghma Khan

Department of Dermatology, University of Wisconsin, Madison, WI

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Deeba N. Syed

Deeba N. Syed

Department of Dermatology, University of Wisconsin, Madison, WI

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Sami Sarfaraz

Sami Sarfaraz

Department of Dermatology, University of Wisconsin, Madison, WI

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Mohammad Abu Zaid

Mohammad Abu Zaid

Department of Dermatology, University of Wisconsin, Madison, WI

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Hasan Mukhtar

Corresponding Author

Hasan Mukhtar

Department of Dermatology, University of Wisconsin, Madison, WI

Fax: +608-263-5223.

Helfaer Professor of Cancer Research, Director and Vice Chair of Research, Department of Dermatology, University of Wisconsin, Medical Sciences Center, Room #B25, 1300 University Avenue, Madison, WI 53706, USASearch for more papers by this author
First published: 11 July 2008
Citations: 39

Abstract

Inhibitors of the epidermal growth factor receptor (EGFR) have generated considerable hope for cancer treatment, specifically for lung and breast cancers. Therefore, identification of a natural, nontoxic agent(s) as an inhibitor of EGFR is of considerable importance. Delphinidin, an anthocyanidin present in pigmented fruits and vegetables, possesses potent antioxidant and antiproliferative properties. In our study, employing EGFR positive breast cancer AU-565 cells and immortalized MCF-10A cells, we evaluated the effect of delphinidin on EGFR and its downstream signaling pathways. Delphinidin (5–40 μM; 3 hr) treatment of both AU-565 cells and MCF-10A cells inhibited the (i) phosphorylation of EGFR, (ii) activation of PI3K, (iii) phosphorylation of AKT and MAPK. Further, delphinidin treatment of AU-565 cells inhibited EGF-induced autophosphorylation of EGFR, AKT and MAPK, activation of PI3K and cell invasion. We then compared the growth inhibitory effects of delphinidin (5–40 μM; 48 hr), and found that it resulted in a decrease in cell growth of AU-565 and MCF-10A cells but had only minimal effects on normal mammary epithelial 184A1 cells. Treatment of AU-565 cells with delphinidin resulted in (i) induction of apoptosis, (ii) cleavage of PARP protein, (iii) activation of caspase-3 and (iv) downregulation of Bcl-2 with an increase in the expression of Bax. In summary, our study identifies a naturally occurring dietary agent delphinidin as an effective inhibitor of EGFR signaling in breast cancer cells. We suggest that delphinidin could be developed as an agent for the management of EGFR positive human cancers. © 2008 Wiley-Liss, Inc.

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