Evidence map›Paper›PMID 16987141›Full record

ArticleCell proliferation2006

An enteroendocrine cell-based model for a quiescent intestinal stem cell niche.

I R Radford, P N Lobachevsky

Open access · bronzeAbstract read
In one paragraph

Article in Cell proliferation, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Cancers · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. The regulatory niche of intestinal stem cells.The Journal of physiology · 2016
    Review
  9. Article
  10. Review
  11. Article
  12. Regeneration of intestinal stem/progenitor cells following doxorubicin treatment of mice.American journal of physiology. Gastrointestinal and liver physiology · 2009
    Article
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

I R RadfordSouth Yarra, Victoria, Australia. ianrradford@optusnet.com.au
P N Lobachevsky
Peter MacCallum Cancer Centre · AUVictoria University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have shown that the kinetics of conversion of intestinal crypt cell populations to a partially or wholly mutant phenotype are consistent with a model in which each crypt contains an infrequently dividing 'deep' stem cell that is the progenitor of several more frequently dividing 'proximate' stem cells. An assumption of our model is that each deep stem cell exists in a growth inhibitory niche. We have used information from the literature to develop a model for a quiescent intestinal stem cell niche. This niche is postulated to be primarily defined by an enteroendocrine cell type that maintains stem cell quiescence by secretion of growth inhibitory peptides such as somatostatin and guanylin/uroguanylin. Consistent with this model, there is evidence that the proteins postulated as defining a growth-inhibitory stem cell niche can act as intestinal tumour suppressors. Confirmation that a growth-inhibitory niche does exist would have important implications for our understanding of intestinal homeostasis and tumorigenesis.

Indexed as

Models, BiologicalAnimalsCell DifferentiationCell LineageEnterocytesEnteroendocrine CellsGastrointestinal HormonesHumansIntestinal MucosaNatriuretic PeptidesSomatostatinStem CellsGastrointestinal HormonesguanylinNatriuretic PeptidesSomatostatinuroguanylin

Identifiers

PMID16987141
PMCPMC6496364
OpenAlexW2032800619

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.