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Transforming growth factor-β and p-21: multiple molecular targets of decorin-mediated suppression of neoplastic growth

Overview of attention for article published in Cell and Tissue Research, April 1999
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (87th percentile)
  • High Attention Score compared to outputs of the same age and source (88th percentile)

Mentioned by

patent
4 patents
wikipedia
9 Wikipedia pages

Citations

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108 Dimensions

Readers on

mendeley
42 Mendeley
Title
Transforming growth factor-β and p-21: multiple molecular targets of decorin-mediated suppression of neoplastic growth
Published in
Cell and Tissue Research, April 1999
DOI 10.1007/s004410051283
Pubmed ID
Authors

Marko Ständer, Ulrike Naumann, Wolfgang Wick, M. Weller

Abstract

Decorin is a member of the small leucine-rich proteoglycan (SLRP) gene family that has recently become a focus in various areas of cancer research. The decorin protein consists of a core protein and a covalently linked glycosaminoglycan chain. Decorin binds to collagens type I, II and IV in vivo and promotes the formation of fibers with increased stability and changes in solubility. Further, the decorin core protein binds to growth factors, including transforming growth factor-beta (TGF-beta), to other intercellular matrix molecules such as fibronectin and thrombospondin, and to the decorin endocytosis receptor. Decorin may directly interfere with the cell cycle via the induction of p21WAF1/CIP1 (p21), a potent inhibitor of cyclin-dependent kinases (CDKs). Here, we discuss interactions of decorin with TGF-beta and with p21, both of which are relevant to carcinogenesis and tumor progression. TGF-beta is released by tumors of various histogenetic origins and promotes immunosuppression in the host and tumor immune escape by induction of growth arrest and apoptosis in immune cells, by downregulation of MHC II antigen expression and by changes in the cytokine release profiles of immune and tumor cells. Moreover, TGF-beta may modulate tumor growth in an autocrine and paracrine fashion, may mediate drug resistance, and may facilitate tumor angiogenesis. Decorin binds to TGF-beta, thus inhibiting its bioactivity, and is a direct or indirect negative modulator of TGF-beta synthesis. Ectopic expression of decorin results in the regression of rat C6 gliomas, an antineoplastic effect attributed to the reversal of TGF-beta-induced immunosuppression. On the other hand, de novo expression of decorin in colon cancer cells and some other tumor cells, even though not in glioma cells, results in an upregulation of p21 expression and a cell cycle arrest, presumably in a TGF-beta-independent manner. Decorin expression is downregulated in many tumors but upregulated in the peritumoral stroma. By virtue of its growth regulatory and immunomodulatory properties, decorin promises to become a novel target for the experimental therapy of human cancers.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 42 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Switzerland 2 5%
Germany 1 2%
Unknown 39 93%

Demographic breakdown

Readers by professional status Count As %
Researcher 14 33%
Student > Ph. D. Student 6 14%
Student > Master 4 10%
Student > Doctoral Student 3 7%
Other 3 7%
Other 5 12%
Unknown 7 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 12 29%
Medicine and Dentistry 8 19%
Biochemistry, Genetics and Molecular Biology 6 14%
Neuroscience 2 5%
Pharmacology, Toxicology and Pharmaceutical Science 1 2%
Other 4 10%
Unknown 9 21%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 9. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 24 December 2017.
All research outputs
#3,798,611
of 25,374,647 outputs
Outputs from Cell and Tissue Research
#145
of 2,232 outputs
Outputs of similar age
#3,004
of 37,037 outputs
Outputs of similar age from Cell and Tissue Research
#2
of 18 outputs
Altmetric has tracked 25,374,647 research outputs across all sources so far. Compared to these this one has done well and is in the 83rd percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 2,232 research outputs from this source. They receive a mean Attention Score of 3.8. This one has done particularly well, scoring higher than 92% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 37,037 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 87% of its contemporaries.
We're also able to compare this research output to 18 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 88% of its contemporaries.