Delphinidin suppresses ultraviolet B-induced cyclooxygenases-2 expression through inhibition of MAPKK4 and PI-3 kinase

Jung Yeon Kwon, Ki Won Lee, Jong Eun Kim, Sung Keun Jung, Nam Joo Kang, Mun Kyung Hwang, Yong Seok Heo, Ann M. Bode, Zigang Dong, Hyong Joo Lee

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82 Scopus citations


Cyclooxygenase-2 (COX-2), a key mediator of inflammation, and its product, prostaglandin E2 (PGE2), enhance carcinogenesis, particularly in skin. Ultraviolet (UV) B is the most carcinogenic component of solar irradiation, and a crucial role of COX-2 in UVB-mediated skin carcinogenesis has been reported. Here, we investigated the effects of delphinidin, an abundant dietary anthocyanin, on UVB-induced COX-2 upregulation and the underlying molecular mechanism. We found that delphinidin suppressed UVB-induced COX-2 expression in JB6 P+ mouse epidermal cells. COX-2 promoter activity and PGE2 production were also suppressed by delphinidin treatment within non-cytotoxic concentrations. Activator protein-1 and nuclear factor-κB, crucial transcription factors involved in COX-2 expression, were activated by UVB and delphinidin abolished this activation. UVB-induced phosphorylation of c-Jun N-terminal kinase, p38 kinase and Akt was inhibited by delphinidin. The activities of mitogen-activated protein kinase kinase (MAPKK) 4 and phosphatidylinositol-3 kinase (PI-3K) were inhibited markedly by delphinidin. A pull-down assay using delphinidin-Sepharose beads revealed that delphinidin binds directly with MAPKK4 or PI-3K in a manner that was competitive with adenosine triphosphate. Moreover, in vivo investigations using mouse skin revealed that the upregulation of COX-2 expression, MAPKK4 activity and PI-3K activity induced by UVB was abolished with delphinidin treatment. Collectively, our results demonstrated that delphinidin targets MAPKK4 and PI-3K directly to suppress COX-2 overexpression, suggesting a potential protective role for delphinidin against UVB-mediated skin carcinogenesis.

Original languageEnglish (US)
Pages (from-to)1932-1940
Number of pages9
Issue number11
StatePublished - 2009

Bibliographical note

Funding Information:
The Hormel Foundation; National Institutes of Health (CA27502, CA120388, CA111536, CA88961, CA 81064); World Class University program (R31-2008-00-10056-0), research grants (Nos. R01-2007-000-11957-0 and M10510140004-08N1014-00410) through the Korea Science and Engineering Foundation funded by the Ministry of Education, Science and Technology; the BioGreen 21 Program (no. 20070301-034-042), Rural Development Administration; Technology Development Program for Agriculture and Forestry (no. 107055-02), Ministry for Food, Agriculture, Forestry and Fisheries, Republic of Korea.


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