(Q44526164)

English

Selective abrogation of the proinvasive activity of the trefoil peptides pS2 and spasmolytic polypeptide by disruption of the EGF receptor signaling pathways in kidney and colonic cancer cells

scientific article published in July 2003

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scholarly article

1 reference

Europe PubMed Central

3 December 2017

Selective abrogation of the proinvasive activity of the trefoil peptides pS2 and spasmolytic polypeptide by disruption of the EGF receptor signaling pathways in kidney and colonic cancer cells (English)

1 reference

Europe PubMed Central

3 December 2017

Christian Gespach

11

object named as

Christian Gespach

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Europe PubMed Central

3 December 2017

author name string

Sylvie Rodrigues

1

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Europe PubMed Central

3 December 2017

Samir Attoub

2

1 reference

Europe PubMed Central

3 December 2017

Quang-Dé Nguyen

3

1 reference

Europe PubMed Central

3 December 2017

Erik Bruyneel

4

1 reference

Europe PubMed Central

3 December 2017

Christelle M Rodrigue

5

1 reference

Europe PubMed Central

3 December 2017

Bruce R Westley

6

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Europe PubMed Central

3 December 2017

Felicity E B May

7

1 reference

Europe PubMed Central

3 December 2017

Lars Thim

8

1 reference

Europe PubMed Central

3 December 2017

Marc Mareel

9

1 reference

Europe PubMed Central

3 December 2017

Shahin Emami

10

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Europe PubMed Central

3 December 2017

language of work or name

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publication date

1 July 2003

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Europe PubMed Central

3 December 2017

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Europe PubMed Central

3 December 2017

22

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Europe PubMed Central

3 December 2017

29

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Europe PubMed Central

3 December 2017

4488-4497

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Europe PubMed Central

3 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.onc.1206685

0 references

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The trefoil factor 1 participates in gastrointestinal cell differentiation by delaying G1-S phase transition and reducing apoptosis

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Homodimerization and hetero-oligomerization of the single-domain trefoil protein pNR-2/pS2 through cysteine 58

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Transcription factor NF-kappaB signals antianoikic function of trefoil factor 3 on intestinal epithelial cells

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Epidermal growth factor receptor activation induces nuclear targeting of cyclooxygenase-2, basolateral release of prostaglandins, and mitogenesis in polarizing colon cancer cells

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Trefoil peptides promote epithelial migration through a transforming growth factor beta-independent pathway

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Cell type specific expression of secretory TFF peptides: colocalization with mucins and synthesis in the brain

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Autocrine transforming growth factor alpha provides a growth advantage to malignant cells by facilitating re-entry into the cell cycle from suboptimal growth states.

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Trefoil peptide protection of intestinal epithelial barrier function: cooperative interaction with mucin glycoprotein

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Growth stimulation and induction of epidermal growth factor receptor by overexpression of cyclooxygenases 1 and 2 in human colon carcinoma cells

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Distinct pathways of cell migration and antiapoptotic response to epithelial injury: structure-function analysis of human intestinal trefoil factor

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Inhibition by platelet-activating factor of Src- and hepatocyte growth factor-dependent invasiveness of intestinal and kidney epithelial cells. Phosphatidylinositol 3'-kinase is a critical mediator of tumor invasion.

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EGFR is a transducer of the urokinase receptor initiated signal that is required for in vivo growth of a human carcinoma

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Impaired defense of intestinal mucosa in mice lacking intestinal trefoil factor.

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The beta(2)-adrenergic receptor mediates extracellular signal-regulated kinase activation via assembly of a multi-receptor complex with the epidermal growth factor receptor

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Constitutive activation of phosphatidylinositol 3-kinase by a naturally occurring mutant epidermal growth factor receptor

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The human trefoil peptide, TFF1, is present in different molecular forms that are intimately associated with mucus in normal stomach

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Transgenic mice that overexpress the human trefoil peptide pS2 have an increased resistance to intestinal damage.

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Epidermal growth factor (EGF) increases the in vitro invasion, motility and adhesion interactions of the primary renal carcinoma cell line, A704.

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Identifiers

10.1038/SJ.ONC.1206685

1 reference

Europe PubMed Central

3 December 2017

1 reference

Europe PubMed Central

3 December 2017

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