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Transforming growth factor β-induced cell cycle arrest of human hematopoietic cells requires p57KIP2 up-regulation

Overview of attention for article published in Proceedings of the National Academy of Sciences of the United States of America, October 2004
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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 (81st percentile)
  • Above-average Attention Score compared to outputs of the same age and source (62nd percentile)

Mentioned by

patent
7 patents

Readers on

mendeley
120 Mendeley
citeulike
1 CiteULike
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Article details
Title
Transforming growth factor β-induced cell cycle arrest of human hematopoietic cells requires p57KIP2 up-regulation
Published in
Proceedings of the National Academy of Sciences of the United States of America, October 2004
DOI 10.1073/pnas.0406771101
Pubmed ID
Authors
Abstract

Transforming growth factor beta (TGFbeta) is one of few known negative regulators of hematopoiesis, yet the mechanisms by which it affects cell cycle arrest and stem cell quiescence are poorly understood. Induction of the cyclin-dependent kinase inhibitors, p15INK4b (p15) and p21WAF1 (p21) is important for TGFbeta-mediated cytostasis in epithelial cells but not in hematopoietic cells. Using primary human hematopoietic cells and microarray analysis, we identified p57KIP2 (p57) as the only cyclin-dependent kinase inhibitor induced by TGFbeta. Up-regulation of p57 mRNA and protein occurs before TGFbeta-induced G1 cell cycle arrest, requires transcription, and is mediated via a highly conserved region of the proximal p57 promoter. The up-regulation of p57 is essential for TGFbeta-induced cell cycle arrest in these cells, because two different small interfering RNAs that prevent p57 up-regulation block the cytostatic effects of TGFbeta on human hematopoietic cells. Reduction of basal p57 expression by this approach also allows hematopoietic cells to proliferate more readily in the absence of TGFbeta. p57 is a putative tumor suppressor gene whose expression is frequently silenced by promoter hypermethylation in hematologic malignancies. Our studies identify a molecular pathway by which TGFbeta mediates its cytostatic effects on human hematopoietic cells and suggests an explanation for the frequent silencing of p57 expression.

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Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 120 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Spain 2 2%
Sweden 1 <1%
Japan 1 <1%
Germany 1 <1%
Unknown 115 96%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 29 24%
Student > Ph. D. Student 17 14%
Student > Bachelor 9 8%
Student > Master 9 8%
Student > Postgraduate 8 7%
Other 17 14%
Unknown 31 26%
Readers by discipline
Readers by discipline Count As %
Agricultural and Biological Sciences 32 27%
Biochemistry, Genetics and Molecular Biology 26 22%
Medicine and Dentistry 14 12%
Immunology and Microbiology 6 5%
Social Sciences 3 3%
Other 7 6%
Unknown 32 27%
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 January 2019.
All research outputs
#5,140,598
of 34,359,530 outputs
Outputs from Proceedings of the National Academy of Sciences of the United States of America
#48,569
of 118,929 outputs
Outputs of similar age
#13,105
of 106,694 outputs
Outputs of similar age from Proceedings of the National Academy of Sciences of the United States of America
#142
of 492 outputs
Altmetric has tracked 34,359,530 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 118,929 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 40.1. This one has gotten more attention than average, scoring higher than 52% 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 106,694 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 81% of its contemporaries.
We're also able to compare this research output to 492 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 62% of its contemporaries.