Suppression of matrix metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN. - Wikidata - wikimedia - TriplyDB

Suppression of matrix metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN.

Suppression of matrix metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN.

http://www.wikidata.org/entity/Q45881488

about

Role of Rap1B and tumor suppressor PTEN in the negative regulation of lysophosphatidic acid--induced migration by isoproterenol in glioma cells Loss of cellular adhesion to matrix induces p53-independent expression of PTEN tumor suppressor The nuclear factor kappa B inhibitor parthenolide restores ICI 182,780 (Faslodex; fulvestrant)-induced apoptosis in antiestrogen-resistant breast cancer cells.Toward a functional annotation of the human genome using artificial transcription factors Phase III study of enzastaurin compared with lomustine in the treatment of recurrent intracranial glioblastoma.Motexafin gadolinium enhances the efficacy of aminolevulinic acid mediated-photodynamic therapy in human glioma spheroids.Osteopontin regulates human glioma cell invasiveness and tumor growth in mice.PTEN augments SPARC suppression of proliferation and inhibits SPARC-induced migration by suppressing SHC-RAF-ERK and AKT signaling.Pten signaling in gliomas.Molecular mechanisms of glioma invasiveness: the role of proteases.Angiopoietin-2 induces human glioma invasion through the activation of matrix metalloprotease-2.Perturbation of hyaluronan interactions inhibits malignant properties of glioma cells Glioblastomas on the move.Modeling prognosis for patients with malignant astrocytic gliomas: quantifying the expression of multiple genetic markers and clinical variables Growth, invasion, metastasis, differentiation, angiogenesis and apoptosis of gastric cancer regulated by expression of PTEN encoding products.Dynamic analysis of glioma cells: looking into "movement phenotypes".Vertebrate animal models of glioma: understanding the mechanisms and developing new therapies.Targeting the PI3K/AKT/mTOR signaling pathway in glioblastoma: novel therapeutic agents and advances in understanding.Differential SKIP expression in PTEN-deficient glioblastoma regulates cellular proliferation and migration.Mechanisms regulating glioma invasion.Investigating the therapeutic role and molecular biology of curcumin as a treatment for glioblastoma Geranylgeranyltransferase I regulates HIF-1α promoting glioblastoma cell migration and invasion.CXCL12-induced glioblastoma cell migration requires intermediate conductance Ca2+-activated K+ channel activity.Cellular and in vivo activity of a novel PI3K inhibitor, PX-866, against human glioblastoma.Overexpression of phospholipase D enhances matrix metalloproteinase-2 expression and glioma cell invasion via protein kinase C and protein kinase A/NF-kappaB/Sp1-mediated signaling pathways.The Rsu-1-PINCH1-ILK complex is regulated by Ras activation in tumor cells.Aberrant FoxM1B expression increases matrix metalloproteinase-2 transcription and enhances the invasion of glioma cells.Neuropilin-1 (NRP-1)/GIPC1 pathway mediates glioma progression.Nuclear PTEN-mediated growth suppression is independent of Akt down-regulation.Inhibition of Necl-5 (CD155/PVR) reduces glioblastoma dispersal and decreases MMP-2 expression and activity.Type 1 insulin-like growth factor regulates MT1-MMP synthesis and tumor invasion via PI 3-kinase/Akt signaling.Regulation of hypoxia inducible factor-1 by nitric oxide in contrast to hypoxia in microvascular endothelium.The tumor suppressor PTEN is exported in exosomes and has phosphatase activity in recipient cells.Matrix metalloproteinase-2 expression by vascular smooth muscle cells is mediated by both stimulatory and inhibitory signals in response to growth factors.INK4a/Arf is required for suppression of EGFR/DeltaEGFR(2-7)-dependent ERK activation in mouse astrocytes and glioma.c-Cbl regulates glioma invasion through matrix metalloproteinase 2.Neuropeptides of the VIP family inhibit glioblastoma cell invasion.Extracellular gamma-synuclein promotes tumor cell motility by activating β1 integrin-focal adhesion kinase signaling pathway and increasing matrix metalloproteinase-24, -2 protein secretion.

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Suppression of matrix metalloproteinase-2 gene expression and invasion in human glioma cells by MMAC/PTEN.

http://www.wikidata.org/entity/Q45881488

description

2001 nî lūn-bûn

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2001年學術文章

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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Suppression of matrix metallop ...... man glioma cells by MMAC/PTEN.

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D Koul

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E N Benvenisite

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J S Rao

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M A Davies

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R Parthasarathy

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R Shen

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S A Jasser

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S K Chintala

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T J Liu

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W K Yung

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P2860

A matrix metalloproteinase expressed on the surface of invasive tumour cells

The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate

Inhibition of cell migration, spreading, and focal adhesions by tumor suppressor PTEN

P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase

Disruption of epithelial cell-matrix interactions induces apoptosis

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

PTEN interactions with focal adhesion kinase and suppression of the extracellular matrix-dependent phosphatidylinositol 3-kinase/Akt cell survival pathway

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

Pten is essential for embryonic development and tumour suppression

Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN

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