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Mutagenicity and tumor-promoting effects of Tiglium seed extract via PKC and MAPK signaling pathways

Authors
Kim, Ji-YoungYun, Jun-WonKim, Yun-SoonKwon, EunaChoi, Hyung JunYeom, Su-CheongKang, Byeong-Cheol
Issue Date
4-Mar-2015
Publisher
TAYLOR & FRANCIS LTD
Keywords
mitogen-activated protein kinases; Tiglium seed; gap junctional intercellular communication; protein kinase C; mutagenicity
Citation
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v.79, no.3, pp.374 - 383
Journal Title
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Volume
79
Number
3
Start Page
374
End Page
383
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10685
DOI
10.1080/09168451.2014.980217
ISSN
0916-8451
Abstract
Tiglium seed is a seed of mature Croton Tiglium Linne containing croton oils, which have been traditionally used as laxative or purgative. As it contains phorbol derivatives, we investigated the mutagenicity and tumor-promoting activity of Tiglium seed. Tiglium seed extract produced the mutagenic responses in five Salmonella typhimurium strains in Ames assay, whereas it did not alter the frequencies of chromosomal aberrations or micronuclei, indicating that it exerted the mutagenic potential, not clastogenicity. Accompanied with phosphorylation of connexin43 (Cx43) and extracellular signal-regulated kinases 1/2 (ERK1/2), Tiglium seed extract inhibited gap junctional intercellular communication (GJIC) associated with tumor-promoting potential. Importantly, these effects were blocked by a protein kinase C (PKC) inhibitor or mitogen-activated protein kinase (MAPKs) inhibitors, suggesting that Tiglium seed-induced GJIC inhibition was regulated by phosphorylation of Cx43 via PKC and MAPKs signaling. In conclusion, Tiglium seed has mutagenicity, possibly linking to tumor-promoting potential through the dysfunction of GJIC.
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