Identification of insulin receptor substrate 1 (IRS-1) and IRS-2 as signaling intermediates in the alpha6beta4 integrin-dependent activation of phosphoinositide 3-OH kinase and promotion of invasion (Q39460470)

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scientific article published on August 2001

Language	Label	Description	Also known as
English	Identification of insulin receptor substrate 1 (IRS-1) and IRS-2 as signaling intermediates in the alpha6beta4 integrin-dependent activation of phosphoinositide 3-OH kinase and promotion of invasion	scientific article published on August 2001

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Identification of insulin receptor substrate 1 (IRS-1) and IRS-2 as signaling intermediates in the alpha6beta4 integrin-dependent activation of phosphoinositide 3-OH kinase and promotion of invasion (English)

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

author name string

L M Shaw

1

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

language of work or name

0 references

publication date

1 August 2001

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Molecular and Cellular Biology

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Europe PubMed Central

PMC publication ID

12 September 2017

21

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

15

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

5082-5093

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Tyrosine phosphorylation of the beta 4 integrin cytoplasmic domain mediates Shc signaling to extracellular signal-regulated kinase and antagonizes formation of hemidesmosomes

1 reference

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Structure, function, and biology of SHIP proteins

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The multiple roles of PTEN in tumor suppression

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RhoA function in lamellae formation and migration is regulated by the alpha6beta4 integrin and cAMP metabolism

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p53 inhibits alpha 6 beta 4 integrin survival signaling by promoting the caspase 3-dependent cleavage of AKT/PKB

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Protein kinase C-dependent mobilization of the alpha6beta4 integrin from hemidesmosomes and its association with actin-rich cell protrusions drive the chemotactic migration of carcinoma cells

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Src-family tyrosine kinases in activation of ERK-1 and p85/p110-phosphatidylinositol 3-kinase by G/CCKB receptors

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New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway

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Release of cAMP gating by the alpha6beta4 integrin stimulates lamellae formation and the chemotactic migration of invasive carcinoma cells

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Insulin receptor substrate-1 as a signaling molecule for focal adhesion kinase pp125(FAK) and pp60(src)

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The COOH-terminal tyrosine phosphorylation sites on IRS-1 bind SHP-2 and negatively regulate insulin signaling

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IL-13 induces tyrosine phosphorylation of phospholipase C gamma-1 following IRS-2 association in human monocytes: relationship with the inhibitory effect of IL-13 on ROI production

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Disruption of IRS-2 causes type 2 diabetes in mice

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The integrin alpha6beta4 functions in carcinoma cell migration on laminin-1 by mediating the formation and stabilization of actin-containing motility structures

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Alphavbeta3 integrin associates with activated insulin and PDGFbeta receptors and potentiates the biological activity of PDGF

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Differential roles of IRS-1 and SHC signaling pathways in breast cancer cells

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Signalling through the lipid products of phosphoinositide-3-OH kinase

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Transformation of chicken cells by the gene encoding the catalytic subunit of PI 3-kinase

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Differential signaling by insulin receptor substrate 1 (IRS-1) and IRS-2 in IRS-1-deficient cells

1 reference

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A carboxy-terminal truncated insulin receptor substrate-1 dominant negative protein reverses the human hepatocellular carcinoma malignant phenotype

1 reference

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Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival

1 reference

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Interaction of insulin receptor substrate-2 (IRS-2) with the insulin and insulin-like growth factor I receptors. Evidence for two distinct phosphotyrosine-dependent interaction domains within IRS-2

1 reference

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The Fyn tyrosine kinase binds Irs-1 and forms a distinct signaling complex during insulin stimulation

1 reference

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The proto-oncogene product c-Crk associates with insulin receptor substrate-1 and 4PS. Modulation by insulin growth factor-I (IGF) and enhanced IGF-I signaling

1 reference

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Cell migration: a physically integrated molecular process

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The type I interferon receptor mediates tyrosine phosphorylation of insulin receptor substrate 2

1 reference

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Nck associates with the SH2 domain-docking protein IRS-1 in insulin-stimulated cells

1 reference

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Role of IRS-1-GRB-2 complexes in insulin signaling

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A novel structural variant of the human beta 4 integrin cDNA

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Signal transduction by the alpha 6 beta 4 integrin: distinct beta 4 subunit sites mediate recruitment of Shc/Grb2 and association with the cytoskeleton of hemidesmosomes

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Non-SH2 domains within insulin receptor substrate-1 and SHC mediate their phosphotyrosine-dependent interaction with the NPEY motif of the insulin-like growth factor I receptor

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Specificity in recognition of phosphopeptides by src-homology 2 domains.

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Interleukins 2, 4, 7, and 15 stimulate tyrosine phosphorylation of insulin receptor substrates 1 and 2 in T cells. Potential role of JAK kinases

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Cloning and sequence analysis of beta-4 cDNA: an integrin subunit that contains a unique 118 kd cytoplasmic domain

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Epithelial integrin alpha 6 beta 4: complete primary structure of alpha 6 and variant forms of beta 4

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Structure of the insulin receptor substrate IRS-1 defines a unique signal transduction protein

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IRS-1 activates phosphatidylinositol 3'-kinase by associating with src homology 2 domains of p85

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Interferon-dependent activation of the serine kinase PI 3'-kinase requires engagement of the IRS pathway but not the Stat pathway

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Association of insulin receptor substrate-1 with integrins

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Identifiers

10.1128/MCB.21.15.5082-5093.2001

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

release_t7x4alfbffhi5ncjc3nocrhud4

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

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