7-Methoxy-luteolin-8-C-β-6-deoxy-xylo-pyranos-3-uloside exactly (mLU8C-PU) isolated from Arthraxon hispidus inhibits migratory and invasive responses mediated via downregulation of MMP-9 and IL-8 expression in MCF-7 breast cancer cells.
Soo-Jin KimThu-Huyen PhamYesol BakHyung-Won RyuSei-Ryang OhDo-Young YoonPublished in: Environmental toxicology (2018)
7-Methoxy-luteolin-8-C-β-6-deoxy-xylo-pyranos-3-uloside (mLU8C-PU) is a glycosylflavone of luteolin isolated from Arthraxon hispidus (Thunb.). Luteolin is known to exert anti-migratory and anti-invasive effects on tumor cells. However, there are no reports on the effects of mLU8C-PU on tumor invasiveness and associated signaling pathways. In this study, we demonstrated the anti-migratory and anti-invasive effects of mLU8C-PU in 12-O-tetradecanoylphorbol-13-acetate (TPA)-treated MCF-7 breast cancer cells. We also investigated the effect of mLU8C-PU on invasion- related signal transducers, including protein kinase Cα (PKCα), c-Jun N terminal kinase (JNK), activator protein-1 (AP-1), and nuclear factor-kappa B (NF-ĸB). TPA-induced membrane translocation of PKCα, phosphorylation of JNK, and the nuclear translocations of AP-1 and NF-κB were downregulated by mLU8C-PU in MCF-7 cells. In addition, mLU8C-PU also inhibited matrix metalloproteinase-9 (MMP-9) and interleukin-8 (IL-8) expression. These results indicate that mLU8C-PU inhibits migratory and invasive responses in MCF-7 breast cancer cells by suppressing MMP-9 and IL-8 expression through mitigating TPA-induced PKCα, JNK activation, and the nuclear translocation of AP-1 and NF-κB. These results suggest that mLU8C-PU may be used as an anti-metastatic agent.
Keyphrases
- breast cancer cells
- nuclear factor
- signaling pathway
- protein kinase
- induced apoptosis
- toll like receptor
- poor prognosis
- pi k akt
- cell death
- cell migration
- oxidative stress
- lps induced
- epithelial mesenchymal transition
- transcription factor
- high glucose
- cell proliferation
- squamous cell carcinoma
- small cell lung cancer
- cell cycle arrest
- endothelial cells
- emergency department
- diabetic rats
- endoplasmic reticulum stress
- tyrosine kinase
- long non coding rna
- small molecule
- drug induced
- atomic force microscopy
- mass spectrometry
- protein protein