The tumor suppressor RECK interferes with HER-2/Neu dimerization and attenuates its oncogenic signaling (Q24337918)

identical protein binding

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Kun-Jing Hong

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Ming-Chuan Hsu

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Ming-Fen Hou

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Wen-Chun Hung

Regulation of matrix metalloproteinase-9 and inhibition of tumor invasion by the membrane-anchored glycoprotein RECK

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language of work or name

English

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publication date

18 February 2011

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published in

FEBS Letters

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volume

585

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issue

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page(s)

591-5

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cites work

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The membrane-anchored MMP inhibitor RECK is a key regulator of extracellular matrix integrity and angiogenesis

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RECK gene expression in hepatocellular carcinoma: correlation with invasion-related clinicopathological factors and its clinical significance. Reverse-inducing--cysteine-rich protein with Kazal motifs

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HER-2/neu represses the metastasis suppressor RECK via ERK and Sp transcription factors to promote cell invasion

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RECK is a target of Epstein–Barr virus latent membrane protein 1

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Involvement of histone deacetylation in ras-induced down-regulation of the metastasis suppressor RECK.

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Silencing of the metastasis suppressor RECK by RAS oncogene is mediated by DNA methyltransferase 3b-induced promoter methylation

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The Kazal motifs of RECK protein inhibit MMP-9 secretion and activity and reduce metastasis of lung cancer cells in vitro and in vivo

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Endosomal transport of ErbB-2: mechanism for nuclear entry of the cell surface receptor

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Overexpression of Jab1 in hepatocellular carcinoma and its inhibition by peroxisome proliferator-activated receptor{gamma} ligands in vitro and in vivo

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Ligand and p185c-neu density govern receptor interactions and tyrosine kinase activation

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Up-regulation of miR-21 by HER2/neu signaling promotes cell invasion.

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MicroRNA expression and regulation in mouse uterus during embryo implantation

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MicroRNA 21 promotes glioma invasion by targeting matrix metalloproteinase regulators

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Crystal structure of the first three domains of the type-1 insulin-like growth factor receptor

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Disabling receptor ensembles with rationally designed interface peptidomimetics

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HER2/neu: mechanisms of dimerization/oligomerization

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The ß1-integrin-dependent function of RECK in physiologic and tumor angiogenesis

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Hypoxia and RAS-signaling pathways converge on, and cooperatively downregulate, the RECK tumor-suppressor protein through microRNAs

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