(Q37090431)

English

Bone morphogenetic proteins induce pancreatic cancer cell invasiveness through a Smad1-dependent mechanism that involves matrix metalloproteinase-2.

scientific article published on 04 December 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Bone morphogenetic proteins induce pancreatic cancer cell invasiveness through a Smad1-dependent mechanism that involves matrix metalloproteinase-2. (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

1 reference

based on heuristic

inferred from title

pancreatic cancer

1 reference

based on heuristic

inferred from title

neoplastic invasiveness

1 reference

based on heuristic

inferred from title

4

object named as

Gerard C Blobe

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Kelly J Gordon

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Kellye C Kirkbride

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tam How

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

language of work or name

0 references

publication date

4 December 2008

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

30

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

238-248

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2639045/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Redox mechanisms switch on hypoxia-dependent epithelial-mesenchymal transition in cancer cells

1 reference

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Expression of the type III TGF-beta receptor is negatively regulated by TGF-beta

1 reference

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Bone morphogenetic proteins signal through the transforming growth factor-beta type III receptor

1 reference

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1 reference

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Loss of type III transforming growth factor beta receptor expression increases motility and invasiveness associated with epithelial to mesenchymal transition during pancreatic cancer progression

1 reference

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Bone morphogenetic protein 4 induces epithelial-mesenchymal transition through MSX2 induction on pancreatic cancer cell line

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The type III TGF-beta receptor suppresses breast cancer progression

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Smad4 is dispensable for normal pancreas development yet critical in progression and tumor biology of pancreas cancer

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Complex networks orchestrate epithelial-mesenchymal transitions

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Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning

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Bone morphogenetic protein 2 stimulation of tumor growth involves the activation of Smad-1/5.

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Identification of receptors and signaling pathways for orphan bone morphogenetic protein/growth differentiation factor ligands based on genomic analyses

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Diverse biological effect and Smad signaling of bone morphogenetic protein 7 in prostate tumor cells

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BMP receptor signaling: transcriptional targets, regulation of signals, and signaling cross-talk

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SCF(beta-TrCP1) controls Smad4 protein stability in pancreatic cancer cells

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Microarray analysis of metastasis-associated gene expression profiling in a murine model of thyroid carcinoma pulmonary metastasis: identification of S100A4 (Mts1) gene overexpression as a poor prognostic marker for thyroid carcinoma

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Pancreatic cancer

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New functions for the matrix metalloproteinases in cancer progression

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Bone morphogenetic protein 2 exerts diverse effects on cell growth in vitro and is expressed in human pancreatic cancer in vivo

1 reference

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1 reference

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based on heuristic

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TGF-?-induced invasiveness of pancreatic cancer cells is mediated by matrix metalloproteinase-2 and the urokinase plasminogen activator system

1 reference

https://pubmed.ncbi.nlm.nih.gov/19056927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/19056927

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/CARCIN/BGN274

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

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