Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
about
Thiopeptide antibiotics: retrospective and recent advancesThiostrepton and derivatives exhibit antimalarial and gametocytocidal activity by dually targeting parasite proteasome and apicoplastFOXM1 in sarcoma: role in cell cycle, pluripotency genes and stem cell pathwaysRETRACTED: Gene-gene interaction network analysis of ovarian cancer using TCGA dataThioFinder: a web-based tool for the identification of thiopeptide gene clusters in DNA sequencesFOXM1 is an oncogenic mediator in Ewing SarcomaPeroxiredoxin 3 is a redox-dependent target of thiostrepton in malignant mesothelioma cellsDeletion of Forkhead Box M1 transcription factor from respiratory epithelial cells inhibits pulmonary tumorigenesis.FoxM1 is a general target for proteasome inhibitors.MiR-370 sensitizes chronic myeloid leukemia K562 cells to homoharringtonine by targeting Forkhead box M1Identification of neuron selective androgen receptor inhibitors.Forkhead box M1 transcription factor: a novel target for cancer therapy.Thiazole antibiotic thiostrepton synergize with bortezomib to induce apoptosis in cancer cells.Phosphorylation of the HIV-1 capsid by MELK triggers uncoating to promote viral cDNA synthesis.Forkhead box L1 is frequently downregulated in gallbladder cancer and inhibits cell growth through apoptosis induction by mitochondrial dysfunction.New potential anti-cancer agents synergize with bortezomib and ABT-737 against prostate cancer.FoxM1 mediates resistance to herceptin and paclitaxel.Aberrant activation of ERK/FOXM1 signaling cascade triggers the cell migration/invasion in ovarian cancer cells.Production of a new thiopeptide antibiotic, TP-1161, by a marine Nocardiopsis species.Suppression of FOXM1 sensitizes human cancer cells to cell death induced by DNA-damage.Binding induced RNA conformational changes control substrate recognition and catalysis by the thiostrepton resistance methyltransferase (Tsr).FoxM1 is a novel target of a natural agent in pancreatic cancer.Down-regulation of FoxM1 by thiostrepton or small interfering RNA inhibits proliferation, transformation ability and angiogenesis, and induces apoptosis of nasopharyngeal carcinoma cells.Negative regulation of the oncogenic transcription factor FoxM1 by thiazolidinediones and mithramycin.Overexpression of FOXM1 is associated with metastases of nasopharyngeal carcinomaGenome-wide expression analysis of Middle Eastern colorectal cancer reveals FOXM1 as a novel target for cancer therapyStructural basis and dynamics of multidrug recognition in a minimal bacterial multidrug resistance system.Azithromycin synergistically enhances anti-proliferative activity of vincristine in cervical and gastric cancer cells.ROS inhibitor N-acetyl-L-cysteine antagonizes the activity of proteasome inhibitorsSorafenib inhibits proliferation and invasion of human hepatocellular carcinoma cells via up-regulation of p53 and suppressing FoxM1.Heterologous expression of the thiopeptide antibiotic GE2270 from Planobispora rosea ATCC 53733 in Streptomyces coelicolor requires deletion of ribosomal genes from the expression construct.Identification of the thiazolyl peptide GE37468 gene cluster from Streptomyces ATCC 55365 and heterologous expression in Streptomyces lividans.Identification of FOXM1 as a therapeutic target in B-cell lineage acute lymphoblastic leukaemia.Quinoline-based clioquinol and nitroxoline exhibit anticancer activity inducing FoxM1 inhibition in cholangiocarcinoma cells.Micelle-encapsulated thiostrepton as an effective nanomedicine for inhibiting tumor growth and for suppressing FOXM1 in human xenografts.A FOXM1 Dependent Mesenchymal-Epithelial Transition in Retinal Pigment Epithelium Cells.The suppression of FOXM1 and its targets in breast cancer xenograft tumors by siRNAThiostrepton is an inducer of oxidative and proteotoxic stress that impairs viability of human melanoma cells but not primary melanocytesNucleophosmin interacts with FOXM1 and modulates the level and localization of FOXM1 in human cancer cells.Investigation of FOXM1 as a Potential New Target for Melanoma.
P2860
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P2860
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@en
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@nl
type
label
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@en
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@nl
prefLabel
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@en
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@nl
P2093
P2860
P1433
P1476
Thiazole antibiotics target FoxM1 and induce apoptosis in human cancer cells.
@en
P2093
Andrei L Gartel
Marianna Halasi
Uppoor G Bhat
P2860
P356
10.1371/JOURNAL.PONE.0005592
P407
P577
2009-05-18T00:00:00Z