2015
DOI: 10.1016/j.jss.2014.12.013
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Artemisinin inhibits the proliferation, migration, and inflammatory reaction induced by tumor necrosis factor-α in vascular smooth muscle cells through nuclear factor kappa B pathway

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Cited by 41 publications
(25 citation statements)
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“…In addition, the expression levels of cyclin D1, cyclin E, CDK2, and CDK4 were downregulated by ART in a dose‐dependent manner, resulting in blocking the G0/G1 and G1/S checkpoint; this may eventually induce G1 phase cell cycle arrest and inhibit the proliferation of TNF‐ α ‐stimulated VSMC. We previously confirmed that ART inhibits the proliferation, migration, and inflammatory reaction induced by TNF‐ α in VSMC through the nuclear factor kappa B pathway . Moreover, it has also been reported that ART attenuates lipopolysaccharide‐stimulated pro‐inflammatory responses by inhibiting the nuclear factor kappa B pathway in microglia cells .…”
Section: Discussionsupporting
confidence: 64%
“…In addition, the expression levels of cyclin D1, cyclin E, CDK2, and CDK4 were downregulated by ART in a dose‐dependent manner, resulting in blocking the G0/G1 and G1/S checkpoint; this may eventually induce G1 phase cell cycle arrest and inhibit the proliferation of TNF‐ α ‐stimulated VSMC. We previously confirmed that ART inhibits the proliferation, migration, and inflammatory reaction induced by TNF‐ α in VSMC through the nuclear factor kappa B pathway . Moreover, it has also been reported that ART attenuates lipopolysaccharide‐stimulated pro‐inflammatory responses by inhibiting the nuclear factor kappa B pathway in microglia cells .…”
Section: Discussionsupporting
confidence: 64%
“…Inflammatory cytokines, including TNF- α , are known to trigger invasion of HASMCs mediated by matrix metalloproteinases [16, 17]. Our results here show that treatment with ZNE (100 and 150  μ g/ml) inhibited HASMC invasion of the Matrigel-coated filter inserts.…”
Section: Resultssupporting
confidence: 51%
“…in their 2014 study that reported a similar depletion of CD4 + CD25 + FOXP3 + Treg in mouse cervical cancer models, with a corresponding inhibition of PGE 2 (prostaglandin E2) production and FOXP3 downregulation . This reduction in PGE 2 corroborates with a subsequent study in smooth muscle cells . Changes in signaling molecule production however is likely to be cell‐line dependent, as demonstrated by Cui et al.…”
Section: Molecular Targets and Signaling Pathways Implicated In The Amentioning
confidence: 99%