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Multicarotenoids at Physiological Levels Inhibit Metastasis in Human Hepatocarcinoma SK-Hep-1 Cells. | LitMetric

AI Article Synopsis

  • Multiple studies confirm that single carotenoids like lycopene and β-carotene have anti-metastatic effects, but the impact of multicarotenoids is less understood.
  • This research specifically examined the effects of multicarotenoids found in Taiwanese and American populations on human liver cancer cells, showing that both forms significantly reduced cell invasion, migration, and adhesion.
  • The adjustments in matrix metalloproteinase activities and protein expressions suggest that multicarotenoids might be effective in preventing cancer metastasis, though further studies in live subjects are essential to verify these results.

Article Abstract

Several studies have demonstrated that single carotenoid, including lycopene, β-carotene, and α-carotene, exhibits antimetastatic effects; however, little is known whether multicarotenoids have similar effects. Herein, we investigated the antimetastatic effect of multicarotenoids at physiological serum levels in Taiwanese (MCT at 1.4 μM) and American (MCA at 1.8 μM) populations using human hepatocarcinoma SK-Hep-1 cells in comparison with single carotenoid, such as lycopene (0.3 or 0.6 μM, respectively), α-carotene (0.1 μM), β-carotene (0.4 μM), lutein (0.4 or 0.5 μM, respectively), and β-cryptoxanthin (0.2 μM). Results reveal that MCA treatment exhibited an additive inhibition on invasion, migration and adhesion at 24 and 48 h of incubation, whereas MCT treatment possessed additive inhibition at 48 h of incubation. The antimetastatic action of MCT and MCA involved additive reduction on activities of matrix metalloproteinase (MMP)-2, -9, and protein expression of Rho and Rac 1 but additive promotion on protein expression of tissue inhibitor of MMP (TIMP)-1 and -2. All of these effects were stronger in MCA than in MCT at 24 and 48 h of incubation. These results demonstrate that multi-carotenoids effectively inhibit metastasis of human hepatocarcinoma SK-Hep-1 cells. More in vivo studies are needed to confirm these findings.

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Source
http://dx.doi.org/10.1080/01635581.2015.1019633DOI Listing

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