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Keywords
(15)
Actin Cytoskeleton
Cancer Patient
Cause of Death
Cell Invasion
matrix metalloproteinase
Molecular Data
Non Small Cell Lung Cancer
Protein Kinase
Signaling Pathway
Urokinase Type Plasminogen Activator
Wound Healing
activator protein 1
Lung Cancer
Mitogen Activated Protein Kinase Kinase
Nuclear Factor Kappa B
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Acacetin inhibits the invasion and migration of human non-small cell lung cancer A549 cells by suppressing the p38α MAPK signaling pathway
Acacetin inhibits the invasion and migration of human non-small cell lung cancer A549 cells by suppressing the p38α MAPK signaling pathway,10.1007/s11
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Acacetin inhibits the invasion and migration of human non-small cell lung cancer A549 cells by suppressing the p38α MAPK signaling pathway
(
Citations: 1
)
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Shang-Tao Chien
,
Su-Shun Lin
,
Cheng-Kun Wang
,
Yuan-Bin Lee
,
Kun-Shiang Chen
,
Yao Fong
,
Yuan-Wei Shih
Lung cancer
is one of the most common malignancies in the world and its metastasis is the major
cause of death
in cancer patients. Acacetin (5,7-dihydroxy-4′-methoxyflavone), a flavonoid compound, has anti-peroxidative and anti-inflammatory effects. The effect of acacetin on invasion and migration in human NSCLC A549 cells was investigated. First, the result demonstrated acacetin could exhibit an inhibitory effect on the abilities of the adhesion, morphology/actin cytoskeleton arrangement, invasion, and migration by cell–matrix adhesion assay, immunofluorescence assay, Boyden chamber assay, and wound-healing assay.
Molecular data
showed that the effect of acacetin in A549 cells might be mediated via sustained inactivation of the phosphorylation of mixed-lineage
protein kinase
3 (MLK3), mitogen-activated
protein kinase
kinases 3/6 (MKK3/6), and p38α MAPK signal involved in the downregulation of the expressions of matrix metalloproteinase-2 (MMP-2), matrix metalloproteinase-9 (MMP-9), and urokinase-type
plasminogen activator
(u-PA). Next, acacetin significantly decreased in the phosphorylation and degradation of inhibitor of kappaBα (IκBα), and the nuclear levels of
nuclear factor kappa B
(NF-κB), c-Fos, and c-Jun. Also, the treatment with acacetin to A549 cells also leads to a concentration-dependent inhibition on the binding abilities of NF-κB and activator protein-1 (AP-1). Furthermore, the treatment of specific inhibitor for p38 MAPK (SB203580) to A549 cells could cause reduced activities of MMP-2/9 and u-PA. In addition, acacetin significantly decreased the levels of phospho-p38α MAPK, MMP-2/9, and u-PA in p38α-cDNA-transfected cells concomitantly with a marked reduction on
cell invasion
and migration. Our results revealed the anti-migration and anti-invasion effects of acacetin, which may act as a promising therapeutic agent for the treatment of lung cancer.
Journal:
Molecular and Cellular Biochemistry - MOL CELL BIOCHEM
, vol. 350, no. 1, pp. 135-148, 2011
DOI:
10.1007/s11010-010-0692-2
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Citations
(1)
Phase II cancer clinical trials with a one-sample log-rank test and its corrections based on the Edgeworth expansion
Xiaoqun Sun
,
Paul Peng
,
Dongsheng Tu
Journal:
Contemporary Clinical Trials - CONTEMP CLIN TRIALS
, vol. 32, no. 1, pp. 108-113, 2011