4.7 Article

Antiproliferative and cytotoxic effects of green coffee and yerba mate extracts, their main hydroxycinnamic acids, methylxanthine and metabolites in different human cell lines

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 106, 期 -, 页码 125-138

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2017.05.019

关键词

Cancer; Yerba mate; Green coffee beans; Hydroxycinnamic acid metabolites

资金

  1. Spanish Ministry of Economy and Competitivity (MINECO-FEDER) [AGL2010-18269, AGL2015-69986-R]
  2. CSIC [PIE-201670E061]
  3. CSIC
  4. European Social Funds
  5. China Scholarship Council

向作者/读者索取更多资源

This work aimed at studying the effects of green coffee bean (GCBE) and yerba mate (YME) extracts, their main phenolic components (5-caffeoylquinic acid, 5-CQA; 3,5-dicaffeoylquinic acid, 3,5-DCQA) and metabolites (ferulic acid, FA; caffeic acid, CA; dihydrocaffeic acid, DHCA; and dihydroferulic acid, DHFA) along with caffeine (CAF) on the viability and proliferation of different human cell lines. Extracts (10-1000 mu g/mL) and standards (10-1000 mu M) were assayed in colon (Caco-2), lung (A549), oesophageal (OE-33), urinary bladder (T24) human carcinoma cells, and a non-cancer cell line (CCD-18Co). YME significantly reduced viability of cancer cells at all assayed concentrations, the higher doses also reducing cell proliferation. GCBE effects on cell viability were more effective at 100 and 1000 mu g/mL, showing modest effects on cell proliferation. The highest doses of 5-CQA and 3,5-DCQA reduced cell viability and proliferation in all cell lines, whereas FA, DHCA and DHFA had lower and variable effects. Caffeine had no effect. Dietary-attainable concentrations (0.1, 1 and 10 mu g/mL) of YME were tested for cytotoxicity and reactive oxygen species generation, showing no cytotoxic effect. Low concentrations of all tested compounds were non-cytotoxic to CCD-18Co cells. Conclusion: YME and to a lower degree GCBE, their phenolic components and metabolites may decrease cancer cell viability and proliferation. (C) 2017 Elsevier Ltd. All rights reserved.

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