Abstract
Claudin-2 is highly expressed in human lung adenocarcinoma tissues and may be a novel target for cancer chemotherapy because knockdown of claudin-2 decreases cell proliferation. We found that flavonoids including kaempferol, chrysin, and luteolin concentration-dependently decrease claudin-2 expression in lung adenocarcinoma A549 cells. Claudin-2 expression is up-regulated by mitogen-activated protein kinase kinase (MEK)/ extracellular signal-regulated kinase (ERK)/c-Fos and phosphoinositide 3-kinase (PI3K)/Akt/nuclear factor-κB (NF-κB) pathways, but these activities were not inhibited by kaempferol, chrysin, and luteolin. Promoter deletion assay using luciferase reporter vector showed that kaempferol and luteolin inhibit the function of transcriptional factor that binds to the region between −395 and −144 of claudin-2 promoter. The decrease in promoter activity was suppressed by mutation in signal transducers and activators of transcription (STAT)-binding site, which is located between −395 and −144. The phosphorylation level of STAT3 was not decreased, but the binding of STAT3 on the promoter region is suppressed by kaempferol and luteolin in chromatin immunoprecipitation assay. The inhibition of cell proliferation caused by kaempferol and luteolin was partially recovered by ectopic claudin-2 expression. Taken together, kaempferol and luteolin decreased claudin-2 expression and proliferation in A549 cells mediated by the inhibition of binding of STAT3 on the promoter region of claudin-2. The intake of foods and nutrients rich in these flavonoids may prevent lung adenocarcinoma development.
Highlights
Epithelial cells form tight junctions (TJs) at the most apical pole of the lateral membrane between neighboring cells
We focused on the regulatory mechanism of which kaempferol, chrysin, and luteolin decrease claudin-2 expression because the effects of these flavonoids are the strongest
We found that kaempferol, chrysin, and luteolin decrease the mRNA and protein levels of claudin-2 in lung adenocarcinoma A549 cells
Summary
Epithelial cells form tight junctions (TJs) at the most apical pole of the lateral membrane between neighboring cells. The TJs regulate the flux of ions and solutes through the paracellular pathway, cell proliferation, polarization, and differentiation [1,2,3]. Most solid cancers are derived from epithelial tissues and disruption of polarity accelerates cell proliferation and differentiation. Claudins are integral membrane proteins of TJs and comprise a large family of 27 subtypes in a mammal [4,5]. Dysregulation of claudins expression has been shown in various tumor tissues [6]. We have been reported that the expression of claudin-2 is up-regulated in human lung adenocarcinoma tissues [7]. The elevation of claudin-2 expression is reported in liver [8], colon [9], and stomach cancer tissues [10]
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