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An Osteoblast-Derived Proteinase Controls Tumor Cell Survival via TGF-beta Activation in the Bone Microenvironment

Overview of attention for article published in PLOS ONE, January 2012
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Title
An Osteoblast-Derived Proteinase Controls Tumor Cell Survival via TGF-beta Activation in the Bone Microenvironment
Published in
PLOS ONE, January 2012
DOI 10.1371/journal.pone.0029862
Pubmed ID
Authors

Sophie Thiolloy, James R. Edwards, Barbara Fingleton, Daniel B. Rifkin, Lynn M. Matrisian, Conor C. Lynch

Abstract

Breast to bone metastases frequently induce a "vicious cycle" in which osteoclast mediated bone resorption and proteolysis results in the release of bone matrix sequestered factors that drive tumor growth. While osteoclasts express numerous proteinases, analysis of human breast to bone metastases unexpectedly revealed that bone forming osteoblasts were consistently positive for the proteinase, MMP-2. Given the role of MMP-2 in extracellular matrix degradation and growth factor/cytokine processing, we tested whether osteoblast derived MMP-2 contributed to the vicious cycle of tumor progression in the bone microenvironment.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 44 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Mexico 1 2%
Nigeria 1 2%
Unknown 42 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 18%
Researcher 6 14%
Professor 5 11%
Professor > Associate Professor 5 11%
Student > Master 4 9%
Other 7 16%
Unknown 9 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 19 43%
Medicine and Dentistry 7 16%
Biochemistry, Genetics and Molecular Biology 2 5%
Immunology and Microbiology 1 2%
Pharmacology, Toxicology and Pharmaceutical Science 1 2%
Other 2 5%
Unknown 12 27%