2008
DOI: 10.1016/j.ejphar.2008.02.076
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YSK2821, a newly synthesized indoledione derivative, inhibits cell proliferation and cell cycle progression via the cell cycle-related proteins by regulating phosphatidylinositol-3 kinase cascade in vascular smooth muscle cells

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Cited by 13 publications
(6 citation statements)
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“…). Through the phosphorylation and inactivation of pro‐apoptotic proteins, AKT mediates cell survival and growth . Therefore, DMC likely inhibits the ERK1/2‐MAPK and other pro‐proliferative signaling pathways—likely the PI3K/AKT pathway—to regulate serum‐induced VSMC cell proliferation and migration.…”
Section: Discussionmentioning
confidence: 99%
“…). Through the phosphorylation and inactivation of pro‐apoptotic proteins, AKT mediates cell survival and growth . Therefore, DMC likely inhibits the ERK1/2‐MAPK and other pro‐proliferative signaling pathways—likely the PI3K/AKT pathway—to regulate serum‐induced VSMC cell proliferation and migration.…”
Section: Discussionmentioning
confidence: 99%
“…PDGF-ββ binding to the PDGF receptor leads to the activation of several intracellular signaling cascades [29-31]. We next determined whether atorvastatin calcium affects the activation of PDGF-Rβ and its downstream signaling molecules, such as (PI3K)/Akt, (PLC)-γ1 and (ERK) 1/2 (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Level of AKT kinase phosphorylation was increased by serum in our study and GLY inhibited serum-induced phosphorylation of AKT and PI3K, indicating that AKT protein is another potential target for GLY (Figure 4B). AKT mediates cell survival and growth signals by phosphorylating and inactivating pro-apoptotic proteins [34]. Therefore, these results indicate that the ERK1/2-MAPK pathway likely synergizes with other pro-proliferative signaling pathway(s), quite possibly the PI3K/AKT pathway, to regulate serum-induced VSMCs cell proliferation and migration.…”
Section: Discussionmentioning
confidence: 99%