Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
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Treating brain tumors with PDE4 inhibitorsNot so Fast: Co-Requirements for Sonic Hedgehog Induced Brain TumorigenesisAn integrative view on sex differences in brain tumorsTemozolomide is an active agent in children with recurrent medulloblastoma/primitive neuroectodermal tumor: an Italian multi-institutional phase II trial.Growth arrest and forced differentiation of human primary glioblastoma multiforme by a novel small molecule.PDE7B is a novel, prognostically significant mediator of glioblastoma growth whose expression is regulated by endothelial cellsCXCL12 mediates trophic interactions between endothelial and tumor cells in glioblastomaIdentification of novel genetic alterations in samples of malignant glioma patients.Establishment and characterization of clinically relevant models of ependymoma: a true challenge for targeted therapyAn in vivo chemical genetic screen identifies phosphodiesterase 4 as a pharmacological target for hedgehog signaling inhibitionIonizing radiation-induced foci persistence screen to discover enhancers of accelerated senescence.Suppression of G-protein-coupled receptor kinase 3 expression is a feature of classical GBM that is required for maximal growth.Novel chemical library screen identifies naturally occurring plant products that specifically disrupt glioblastoma-endothelial cell interactionsTargeting brain tumor cAMP: the case for sex-specific therapeuticsPhosphodiesterase function and endocrine cells: links to human disease and roles in tumor development and treatmentEvaluation of 9-cis retinoic acid and mitotane as antitumoral agents in an adrenocortical xenograft model.Benzoquinones and terphenyl compounds as phosphodiesterase-4B inhibitors from a fungus of the order Chaetothyriales (MSX 47445).Genomic and functional characterizations of phosphodiesterase subtype 4D in human cancersThe G protein Gαs acts as a tumor suppressor in sonic hedgehog signaling-driven tumorigenesis.Inactivation of oncogenic cAMP-specific phosphodiesterase 4D by miR-139-5p in response to p53 activation.A novel murine model for localized radiation necrosis and its characterization using advanced magnetic resonance imaging.Measuring brain tumor growth: combined bioluminescence imaging-magnetic resonance imaging strategy.Regulation of the Hippo pathway and implications for anticancer drug development.Targeting cancer with phosphodiesterase inhibitors.Clinical and molecular genetics of the phosphodiesterases (PDEs).Current and emerging molecular targets in glioma.Molecular imaging coupled to pattern recognition distinguishes response to temozolomide in preclinical glioblastoma.Novel quinazolin-4(3H)-one/Schiff base hybrids as antiproliferative and phosphodiesterase 4 inhibitors: design, synthesis, and docking studies.Theobromine, the primary methylxanthine found in Theobroma cacao, prevents malignant glioblastoma proliferation by negatively regulating phosphodiesterase-4, extracellular signal-regulated kinase, Akt/mammalian target of rapamycin kinase, and nucleaThe Anti-Warburg Effect Elicited by the cAMP-PGC1α Pathway Drives Differentiation of Glioblastoma Cells into Astrocytes.Downregulation of phosphodiesterase 4B (PDE4B) activates protein kinase A and contributes to the progression of prostate cancer.Phosphodiesterase-4 promotes proliferation and angiogenesis of lung cancer by crosstalk with HIF.Knocking down nucleolin expression in gliomas inhibits tumor growth and induces cell cycle arrest.CXCL12 alone is insufficient for gliomagenesis in Nf1 mutant mice.Protein kinase a in cancerTargeted activation of PKA and Epac promotes glioblastoma regression in vitroCyclic AMP suppression is sufficient to induce gliomagenesis in a mouse model of neurofibromatosis-1The Role of Protein Kinase B Signaling Pathway in Anti-Cancer Effect of Rolipram on Glioblastoma Multiforme: An In Vitro Study.Head and neck cancers, the neglected malignancies: present and future treatment strategies.Ligand/PTC-free intramolecular Heck reaction: synthesis of pyrroloquinoxalines and their evaluation against PDE4/luciferase/oral cancer cell growth in vitro and zebrafish in vivo.
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P2860
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@en
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@nl
type
label
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@en
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@nl
prefLabel
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@en
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@nl
P2093
P2860
P1476
Targeted inhibition of cyclic AMP phosphodiesterase-4 promotes brain tumor regression.
@en
P2093
Andrew Hope
Arie Perry
B Mark Woerner
David D Limbrick
David Piwnica-Worms
Erin Jackson
Joshua B Rubin
Nicole M Warrington
Patricia Goldhoff
P2860
P304
P356
10.1158/1078-0432.CCR-08-0827
P407
P577
2008-12-01T00:00:00Z