Alcohol consumption suppresses mammary tumor metastasis in a syngeneic tumor transplantation model

• Published in: Breast cancer research and treatment 2012-12, Vol.136 (3), p.729-737
• Main Authors: Vorderstrasse, Beth A., Wang, Tao, Myers, Annette K., Wyrick, Katherine L., Meadows, Gary G.
• Format: Article
• Language: English
• Subjects: Alcohol Drinking; Alcohol use; Animals; Biological and medical sciences; Body Weight - drug effects; Breast cancer; Cancer research; Cancer therapies; Drinking of alcoholic beverages; Ethanol - pharmacology; Female; Gynecology. Andrology. Obstetrics; Health aspects; Lung Neoplasms - drug therapy; Lung Neoplasms - metabolism; Lung Neoplasms - secondary; Mammary gland diseases; Mammary Neoplasms, Experimental - epidemiology; Mammary Neoplasms, Experimental - metabolism; Mammary Neoplasms, Experimental - pathology; Medical sciences; Medicine; Medicine & Public Health; Metastasis; Mice; Mice, Inbred BALB C; Oncology; Preclinical Study; Receptors, CXCR4 - metabolism; Rodents; Spleen - drug effects; Transplantation, Isogeneic; Tumor Cells, Cultured; Tumors
• ISSN: 0167-6806; 1573-7217
• DOI: 10.1007/s10549-012-2275-2

Epidemiological studies indicate a positive correlation between alcohol consumption and the risk of developing breast cancer. However, little is known about whether alcohol consumption affects breast cancer metastasis. Considering that the primary cause of death in breast cancer patients is due to metastasis, further insight into whether alcohol consumption influences disease progression and survival is needed. We tested the effect of alcohol consumption on breast cancer metastasis using the 4T1.2 syngeneic mammary tumor model in Balb/c mice. The treatment groups included a High-consuming group (18 % w/v alcohol in drinking water), a Moderate-consuming group (5 % w/v), a Low-consuming group (1 % w/v), and a Water-drinking control group. 4T1.2 mammary tumor cells were injected orthotopically into the mammary fat pad. Metastases were enumerated in lungs and in distant mammary glands 4 weeks after injection. Consumption of High alcohol protected against metastasis, as High-consuming mice typically had 65–75 % fewer metastases compared to Water-drinking controls. A suggestive reduction in tumor spread was observed in the Moderate-drinking group, although the effects did not reach statistical significance. Consumption of the Low alcohol dose did not affect metastasis. CXCR4 expression in the primary tumors was significantly reduced by High alcohol consumption; however, expression of this chemokine receptor in the primary tumor did not correlate with metastatic potential. Additional studies were conducted to test for possible direct effects of 0.3 % w/v ethanol on tumor cell proliferation, migration, invasion, and colony formation of 4T1.2 cells in vitro. Our results indicate that, for this murine model, alcohol consumption does not exacerbate tumor metastasis, and that High alcohol consumption reduces tumor spread.