Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/60400
標題: Advanced Glycation End Products Down-regulate Gap Junctions in Human Hepatoma SKHep 1 Cells via the Activation of Src-Dependent ERK1/2 and JNK/SAPK/AP1 Signaling Pathways
作者: Lin, F.L.
劉宏仁
Chang, C.T.
Chuang, K.P.
Wang, C.Y.
Liu, H.J.
關鍵字: Advanced glycation end products (AGEs)
connexin 32
connexin 43
ERK1/2
JNK/SAPK
intercellular communication
hepatocellular-carcinoma
cancer
chemoprevention
endothelial-cells
expression
connexin-43
apoptosis
liver
carcinogenesis
chemotherapy
期刊/報告no:: Journal of Agricultural and Food Chemistry, Volume 58, Issue 15, Page(s) 8636-8642.
摘要: Hyperglycemia and advanced glycation end products (AGEs) are associated with an elevated risk of developing several cancers in diabetic patients. However, the detailed mechanisms remain to be elucidated. The mechanism of AGE-bovine serum albumin (BSA) on gap junction intercellular communication in human hepatoma cell line, SKHep 1, was investigated. Both Cx32 and Cx43 are major gap junction forming proteins in the liver, the loss of which has been shown to facilitate tumorigenesis. Although the MTT assay results showed that AGE-BSA significantly increased cell growth by 31%, AGE-BSA down-regulated Cx32 and Cx43 expression in a dose- and time-dependent manner. The present study also demonstrated that ERK1/2 and JNK/SAPK were significantly activated by AGE BSA and that Src, ERK1/2, and JNK/SAPK inhibitors significantly reversed the reduction of Cx32 and Cx43 proteins by AGE-BSA. Taken together, these results strongly support the hypothesis that Src-dependent ERK1/2 and JNK/SAPK/AP1 signaling pathways play a key role in AGE BSA-mediated down-regulation of Cx32 and Cx43 protein expression in SKHep 1 cells.
URI: http://hdl.handle.net/11455/60400
ISSN: 0021-8561
文章連結: http://dx.doi.org/10.1021/jf904240c
Appears in Collections:分子生物學研究所

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