AI Article Synopsis

  • Luteolin shows anticancer activity, particularly against triple-negative MDA-MB-231 breast cancer cells, while its glycosides do not have similar effects.
  • Luteolin effectively inhibits migration and invasion of MDA-MB-231 cells and induces apoptosis at certain concentrations, while its glycosides lack both cytotoxic and antimigratory properties.
  • These findings suggest that luteolin may be a promising candidate for breast cancer therapy, based on its distinct effects compared to its glycosides.

Article Abstract

Luteolin is known to have anticancer activity in various cancers. Recent studies have shown that luteolin glycosides, such as luteolin-8--β-fucopyranoside, 7-methoxy-luteolin-8-C-β-(6- deoxyxylopyranos-3-uloside) and luteolin-8-C-β-d-glucopyranoside, flavonoids that are present in , exert antimigratory and anti-invasive effects, but no cytotoxic effect in estrogen receptor-positive MCF7 breast cancer cells. In the present study, we further investigated and compared differential effects of luteolin and its glycosides in MDA-MB-231 triple-negative breast cancer cells. Luteolin suppressed the expression of matrix metalloproteinase-9 and inhibited migration and invasion in MDA-MB-231 cells treated with the tumor promotor 12-O-tetradecanoylphorbol-13-acetate at non-cytotoxic concentrations (0, 5, and 10 μM). Furthermore, at cytotoxic concentrations (20 and 40 μM), luteolin induced apoptosis via extrinsic and intrinsic pathways in MDA-MB-231 cells. However, luteolin glycosides did not exert any cytotoxic, antimigratory, or anti-invasive effect in MDA-MB-231 cells. In brief, luteolin had both antimetastatic and cytotoxic effects on MDA-MB-231 cells, whereas luteolin glycosides had no effect on this cell line. Taking together the present results and our previous findings on the differential effects of luteolin and its glycosides on MDA-MB-231 and MCF-7 breast cancer cells, luteolin and its glycosides can be suggested as a potential candidate for breast cancer therapy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785773PMC
http://dx.doi.org/10.17179/excli2019-1459DOI Listing

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