Melanoma chondroitin sulfate proteoglycan enhances FAK and ERK activation by distinct mechanisms
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Neuron-Glia Interactions in Neural Plasticity: Contributions of Neural Extracellular Matrix and Perineuronal NetsUtilization of Glycosaminoglycans/Proteoglycans as Carriers for Targeted Therapy DeliveryPhosphorylation of NG2 proteoglycan by protein kinase C-alpha regulates polarized membrane distribution and cell motilityRegulation of high molecular weight-melanoma associated antigen (HMW-MAA) gene expression by promoter DNA methylation in human melanoma cellsSuppression subtractive hybridization profiles of radial growth phase and metastatic melanoma cell lines reveal novel potential targets.The progenitor cell marker NG2/MPG promotes chemoresistance by activation of integrin-dependent PI3K/Akt signaling.CSPG4: a prototype oncoantigen for translational immunotherapy studies.Antibody therapies for melanoma: new and emerging opportunities to activate immunity (Review).Functional characterization of an scFv-Fc antibody that immunotherapeutically targets the common cancer cell surface proteoglycan CSPG4Serum free cultured bone marrow mesenchymal stem cells as a platform to characterize the effects of specific moleculesCSPG4 protein as a new target for the antibody-based immunotherapy of triple-negative breast cancerFH535 inhibited migration and growth of breast cancer cells.FGF2 binding, signaling, and angiogenesis are modulated by heparanase in metastatic melanoma cellsNG2 expression in glioblastoma identifies an actively proliferating population with an aggressive molecular signature.A gene expression signature associated with survival in metastatic melanomaChondroitin sulfate proteoglycan 4 functions as the cellular receptor for Clostridium difficile toxin B.Differential phosphorylation of NG2 proteoglycan by ERK and PKCalpha helps balance cell proliferation and migration.CSPG4 as a target of antibody-based immunotherapy for malignant mesotheliomaNew approaches in metastatic melanoma: biological and molecular targeted therapies.NG2/CSPG4-collagen type VI interplays putatively involved in the microenvironmental control of tumour engraftment and local expansion.Focal adhesion kinase: a promising target for anticancer therapy.NG2 expression in microglial cells affects the expression of neurotrophic and proinflammatory factors by regulating FAK phosphorylation.Erythroid cells generated in the absence of specific β1-integrin heterodimers accumulate reactive oxygen species at homeostasis and are unable to mount effective antioxidant defenses.Cell-matrix interactions: focus on proteoglycan-proteinase interplay and pharmacological targeting in cancer.Targeting 11q23 positive acute leukemia cells with high molecular weight-melanoma associated antigen-specific monoclonal antibodiesMelanoma proteoglycan modifies gene expression to stimulate tumor cell motility, growth, and epithelial-to-mesenchymal transitionA role for the NG2 proteoglycan in glioma progression.Divergent Synthesis of Chondroitin Sulfate Disaccharides and Identification of Sulfate Motifs that Inhibit Triple Negative Breast Cancer.Functions of chondroitin sulfate and heparan sulfate in the developing brain.CSPG4, a potential therapeutic target, facilitates malignant progression of melanoma.Roles of NG2 glial cells in diseases of the central nervous system.Targeting of the tumor necrosis factor receptor superfamily for cancer immunotherapy.Transduction of extracellular cues into cell polarity: the role of the transmembrane proteoglycan NG2.Chondroitin sulfate proteoglycan 4 as a target for chimeric antigen receptor-based T-cell immunotherapy of solid tumors.Functional roles of CSPG4/NG2 in chondrosarcoma.A novel approach for targeted elimination of CSPG4-positive triple-negative breast cancer cells using a MAP tau-based fusion protein.Implementation of infrared and Raman modalities for glycosaminoglycan characterization in complex systems.The CSPG4-specific monoclonal antibody enhances and prolongs the effects of the BRAF inhibitor in melanoma cells.Melanoma-associated Chondroitin Sulfate Proteoglycan (MCSP)-targeted delivery of soluble TRAIL potently inhibits melanoma outgrowth in vitro and in vivo.RGD-xyloside conjugates prime glycosaminoglycans.
P2860
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P2860
Melanoma chondroitin sulfate proteoglycan enhances FAK and ERK activation by distinct mechanisms
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@ast
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@en
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@nl
type
label
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@ast
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@en
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@nl
prefLabel
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@ast
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@en
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@nl
P2093
P2860
P3181
P356
P1476
Melanoma chondroitin sulfate p ...... ivation by distinct mechanisms
@en
P2093
Cheryl L Neudauer
Christopher Wilson
James B McCarthy
Jianbo Yang
Matthew A Price
Melanie A Simpson
Soldano Ferrone
P2860
P304
P3181
P356
10.1083/JCB.200403174
P407
P577
2004-06-21T00:00:00Z