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Zeaxanthin inhibits PDGF‐BB‐induced migration in human dermal fibroblasts
Author(s) -
Wu NanLin,
Chiang YuhChiau,
Huang ChiehChen,
Fang JiaYou,
Chen DerFang,
Hung ChiFeng
Publication year - 2010
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2009.01036.x
Subject(s) - zeaxanthin , platelet derived growth factor receptor , fibroblast , cell migration , dermal fibroblast , chemistry , stromal cell , melanoma , microbiology and biotechnology , platelet derived growth factor , human skin , cancer research , cell , growth factor , biochemistry , biology , carotenoid , in vitro , lutein , receptor , genetics
Please cite this paper as : Zeaxanthin inhibits PDGF‐BB‐induced migration in human dermal fibroblasts. Experimental Dermatology 2010; 19 : e173–e181. Abstract: Zeaxanthin is the dihydroxy carotenoid and is distributed in our daily foods. Various natural carotenoids, including zeaxanthin, have been shown to inhibit proliferation of several types of cancer cells, but available data on the effect of zeaxanthin on skin fibroblasts and melanoma cells are limited. Platelet‐derived growth factor (PDGF) functions as a chemotactic factor for dermal fibroblasts and plays an important role in the progression of melanoma. In this study, we investigated the effects of zeaxanthin on the migration of skin fibroblasts induced by PDGF‐BB and melanoma cells. We demonstrated that zeaxanthin inhibited PDGF‐BB‐induced skin fibroblast migration on collagen and gelatin by a modified Boyden chamber system. The electric cell‐substrate impedance sensing (ECIS) method also showed similar inhibitory effects of zeaxanthin on the migration of fibroblasts. In functional studies, zeaxanthin decreased melanoma‐induced fibroblast migration in a non‐contact coculture system and also the migration stimulated by melanoma‐derived conditioned medium. Further analysis showed that zeaxanthin attenuated PDGF‐BB and melanoma‐conditioned medium induced phosphorylation of PDGFR‐β and MAP kinase in a concentration‐dependent manner in human skin fibroblasts. However, these effects did not result from direct interaction of zeaxanthin with PDGF‐BB. Thus, our results provide the first evidence showing that zeaxanthin is an effective inhibitor of migration of stromal fibroblasts induced by PDGF‐BB and melanoma cells and this effect may further support its antitumor potential.