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Cyanidin-3-glucoside inhibits ethanol-induced invasion of breast cancer cells overexpressing ErbB2.

Authors
Xu-M; Bower-KA; Wang-SY; Frank-JA; Chen-G; Ding-M; Wang-SO; Shi-XL; Ke-ZJ; Luo-J
Source
Mol Cancer 2010 Oct; 9:285
NIOSHTIC No.
20038002
Abstract
BACKGROUND: Ethanol is a tumor promoter. Both epidemiological and experimental studies suggest that ethanol may enhance the metastasis of breast cancer cells. We have previously demonstrated that ethanol increased the migration/invasion of breast cancer cells expressing high levels of ErbB2. Amplification of ErbB2 is found in 20-30% of breast cancer patients and is associated with poor prognosis. We sought to identify agents that can prevent or ameliorate ethanol-induced invasion of breast cancer cells. Cyanidin-3-glucoside (C3G), an anthocyanin present in many vegetables and fruits, is a potent natural antioxidant. Ethanol exposure causes the accumulation of intracellular reactive oxygen species (ROS). This study evaluated the effect of C3G on ethanol-induced breast cancer cell migration/invasion. RESULTS: C3G attenuated ethanol-induced migration/invasion of breast cancer cells expressing high levels of ErbB2 (BT474, MDA-MB231 and MCF7(ErbB2)) in a concentration dependent manner. C3G decreased ethanol-mediated cell adhesion to the extracellular matrix (ECM) as well as the amount of focal adhesions and the formation of lamellipodial protrusion. It inhibited ethanol-stimulated phosphorylation of ErbB2, cSrc, FAK and p130(Cas), as well as interactions among these proteins. C3G abolished ethanol-mediated p130(Cas)/JNK interaction. CONCLUSIONS: C3G blocks ethanol-induced activation of the ErbB2/cSrc/FAK pathway which is necessary for cell migration/invasion. C3G may be beneficial in preventing/reducing ethanol-induced breast cancer metastasis.
Keywords
Ethanols; Tumors; Breast-cancer; Cancer; Alcohols; Cell-cultures; Cell-damage; Epidemiology
Contact
Jia Luo, Department of Internal Medicine, University of Kentucky College of Medicine, Lexington, KY 40536, USA
CAS No.
75-07-0
Publication Date
20101029
Document Type
Journal Article
Email Address
jialuo888@uky.edu
Fiscal Year
2011
NTIS Accession No.
NTIS Price
ISSN
1476-4598
NIOSH Division
HELD
Priority Area
Construction; Manufacturing
Source Name
Molecular Cancer
State
KY; MD; WV
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