TGF-beta1 modulates focal adhesion kinase expression in rat intestinal epithelial IEC-6 cells via stimulatory and inhibitory Smad binding elements (Q39908378)

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English	TGF-beta1 modulates focal adhesion kinase expression in rat intestinal epithelial IEC-6 cells via stimulatory and inhibitory Smad binding elements	scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

TGF-beta1 modulates focal adhesion kinase expression in rat intestinal epithelial IEC-6 cells via stimulatory and inhibitory Smad binding elements (English)

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

author name string

Mary F Walsh

1

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

Dinakar R Ampasala

2

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

Arun K Rishi

3

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

Marc D Basson

4

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

publication date

14 November 2008

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

Biochimica et Biophysica Acta

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Europe PubMed Central

PMC publication ID

15 September 2017

1789

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

88-98

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

Transforming growth factor-beta stimulates intestinal epithelial focal adhesion kinase synthesis via Smad- and p38-dependent mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730956

22 September 2017

Molecular requirements for induction of CTGF expression by TGF-beta1 in primary osteoblasts

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Fibroblast growth factor represses Smad-mediated myofibroblast activation in aortic valvular interstitial cells

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Epithelial restitution and wound healing in inflammatory bowel disease

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Structure-function relationship of inhibitory Smads: Structural flexibility contributes to functional divergence

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N-MYC regulates focal adhesion kinase expression in human neuroblastoma.

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TGFbeta1 regulation of vimentin gene expression during differentiation of the C2C12 skeletal myogenic cell line requires Smads, AP-1 and Sp1 family members

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Gene expression regulation and cancer

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Combinatorial activation of FAK and AKT by transforming growth factor-beta1 confers an anoikis-resistant phenotype to myofibroblasts

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Focal adhesion kinase protein levels in gut epithelial motility

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Organization and post-transcriptional processing of focal adhesion kinase gene

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New concepts regarding focal adhesion kinase promotion of cell migration and proliferation

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Transforming growth factor-beta1 induces tissue inhibitor of metalloproteinase-1 expression via activation of extracellular signal-regulated kinase and Sp1 in human fibrosarcoma cells

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ERK1/2 and p38 MAP kinase control MMP-2, MT1-MMP, and TIMP action and affect cell migration: a comparison between mesothelioma and mesothelial cells

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Induced focal adhesion kinase expression suppresses apoptosis by activating NF-kappaB signaling in intestinal epithelial cells

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Smad transcription factors

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Role of Smad proteins in the regulation of NF-kappaB by TGF-beta in colon cancer cells.

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The role of the cytoskeleton in differentially regulating pressure-mediated effects on malignant colonocyte focal adhesion signaling and cell adhesion

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Direct interaction of the N-terminal domain of focal adhesion kinase with the N-terminal transactivation domain of p53

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TGF-beta signaling in colon cancer cells.

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Signaling pathways in intestinal development and cancer

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Sp1 and Smad transcription factors co-operate to mediate TGF-beta-dependent activation of amyloid-beta precursor protein gene transcription.

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Cloning and characterization of the promoter region of human focal adhesion kinase gene: nuclear factor kappa B and p53 binding sites

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Coordinate regulation of cell growth and differentiation by TGF-beta superfamily and Runx proteins

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Multiple connections link FAK to cell motility and invasion

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Mechanisms of TGF-beta signaling from cell membrane to the nucleus

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Links between tumor suppressors: p53 is required for TGF-beta gene responses by cooperating with Smads.

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Focal adhesion kinase signaling activities and their implications in the control of cell survival and motility

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A decade of tyrosine kinases: from gene discovery to therapeutics

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Focal adhesion kinase: the first ten years

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E2F4/5 and p107 as Smad cofactors linking the TGFbeta receptor to c-myc repression

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Inhibition of transforming growth factor (TGF)-beta1-induced extracellular matrix with a novel inhibitor of the TGF-beta type I receptor kinase activity: SB-431542

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Smurf1 interacts with transforming growth factor-beta type I receptor through Smad7 and induces receptor degradation

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Smad7 binds to Smurf2 to form an E3 ubiquitin ligase that targets the TGF beta receptor for degradation

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Transforming growth factor beta signaling mediators and modulators

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Activation of the mitogen-activated protein kinase pathway by transforming growth factor-beta

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Interdependent SMAD and JNK signaling in transforming growth factor-beta-mediated transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/19059368

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Smad and AML proteins synergistically confer transforming growth factor beta1 responsiveness to human germ-line IgA genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19059368

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human caco-2 motility redistributes FAK and paxillin and activates p38 MAPK in a matrix-dependent manner

1 reference

https://pubmed.ncbi.nlm.nih.gov/19059368

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transient activation of NF-kappaB through a TAK1/IKK kinase pathway by TGF-beta1 inhibits AP-1/SMAD signaling and apoptosis: implications in liver tumor formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19059368

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.BBAGRM.2008.11.002

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 September 2017

ResearchGate publication ID

0 references

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