| Literature DB >> 30366081 |
Songlin Chen1, Yunfeng Yi1, Ting Xia1, Zaifa Hong2, Yanmei Zhang3, Ganggang Shi4, Zhimin He4, Shuping Zhong5.
Abstract
Alcohol intake increases the risk of cancer development. Approximately 3.6% human cancers worldwide derive from chronic alcohol drinking, including oral, liver, breast and other organs. Our studies in vivo and in vitro have demonstrated that diluted ethanol increase RNA Pol III gene transcription and promotes cell proliferation and transformation, as well as tumor formation. However, it is unclear about the effect of red wines on the human cancer cells. In present study, we investigated the roles of red wine in human cancer cell growth, colony formation and RNA Pol III gene transcription. Low concentration (12.5 mM to 25 mM) of ethanol enhances cell proliferation of breast and esophageal cancer lines, whereas its higher concentration (100 mM to 200 mM) slightly decreases the rates. In contrast, red wines significantly repress cell proliferation of different human cancer lines from low dose to high dose. The results reveal that the red wine also inhibits colony formation of human breast cancer and esophageal carcinoma cells. The effects of repression on different human cancer lines are in a dose-dependent manner. Further analysis indicates that ethanol increases RNA Pol III gene transcription, whereas the red wines significantly reduce transcription of the genes. Interestingly, the effects of mature wine (brick red) on cancer cell phenotypes are much stronger than young wine (intense violet). Together, these new findings suggest that red wines may contain some bioactive components, which are able to inhibit human cancer cell growth and colony formation.Entities:
Keywords: Cell growth; Colony formation; Ethanol; Human cancer; Pol III genes; Red wine
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Year: 2018 PMID: 30366081 PMCID: PMC6478559 DOI: 10.1016/j.gene.2018.10.049
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688