Evidence map›Paper›PMID 24336194›Full record

ArticleCarcinogenesis2014

Differential effects of 2- and 3-series E-prostaglandins on in vitro expansion of Lgr5+ colonic stem cells.

Yang-Yi Fan, Laurie A Davidson, Evelyn S Callaway, Jennifer S Goldsby, Robert S Chapkin

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Prostaglandin EJournal of cellular and molecular medicine · 2021
    Article
  12. Hyaluronic acid promotes Lgr5American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  13. Article
  14. Review
  15. Article
  16. Establishment of a multicomponent dietary bioactive human equivalent dose to delete damaged Lgr5+ stem cells using a mouse colon tumor initiation model.European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) · 2019
    Article
  17. Review
  18. Murine Colonic Organoid Culture System and Downstream Assay Applications.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
  19. Article
  20. Dietary fat and fiber interactively modulate apoptosis and mitochondrial bioenergetic profiles in mouse colon in a site-specific manner.European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) · 2017
    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

5 authors at 1 institution in 1 country.

Yang-Yi FanProgram in Integrative Nutrition and Complex Diseases.
Laurie A Davidson
Evelyn S Callaway
Jennifer S Goldsby
Robert S Chapkin
Texas A&M University · US

Funding

Gene expression analysis of coding and non-coding RNAs in colon cancer preventionR01CA129444 · NCI · TEXAS A&M UNIVERSITY · PI CHAPKIN, ROBERT STEPHEN · 2007 to 2015
$2.1M
Chemoprotective effects of natural products on colonic adult stem cellsR01CA168312 · NCI · TEXAS A&M UNIVERSITY · PI CHAPKIN, ROBERT STEPHEN, PATIL, BHIMANAGOUDA S. · 2011 to 2015
$1.6M
NCI NIH HHS CA129444NCI NIH HHS CA168312
6 · The paper itself

Abstract

Arachidonic acid (20:4(Δ5,8,11,14), AA)-derived prostaglandin E2 (PGE2) promotes colon cancer development. In contrast, chemoprotective n-3 polyunsaturated fatty acids supplant AA, thereby decreasing PGE2 biosynthesis in colonocytes, with eicosapentaenoic acid (20:5(Δ5,8,11,14,17), EPA) in particular being metabolized to a novel 3-series E-prostaglandin (PGE3), a putative anti-tumorigenic-cyclooxygenase metabolite. Because transformation of adult stem cells is an extremely important route toward initiating intestinal cancer, we utilized the leucine-rich-repeat-containing G-protein-coupled receptor 5 (Lgr5)-enhanced green fluorescent protein-internal ribosome entry site (IRES)-creER(T2) knock-in mouse model to isolate and culture colonic organoids, in order to document ex vivo responses to exogenous PGE2 and PGE3. Colonic crypts were isolated from transgenic mice and cultured in a Matrigel-based three-dimensional platform. Organoids were treated with exogenous PGE2, PGE3 or dimethyl sulfoxide (vehicle control) for 5 days and the number of viable organoids was recorded daily. Subsequently, samples were processed for immunohistochemistry, flow cytometry and real-time PCR analyses. PGE2 promoted optimal organoid growth and induced significantly higher levels of cell proliferation (P < 0.05) compared with PGE3 and control. In contrast, the Lgr5-green fluorescent protein-positive stem cell number was uniquely elevated by >2-fold in PGE2-treated cultures compared with PGE3 and control. This coincided with the upregulation of stem-cell-related Sox9, Axin2 and Cd44 messenger RNAs. Our results demonstrate that relative to AA-derived PGE2, a known promoter of colon tumorigenesis, EPA-derived PGE3 has diminished ability to support colonic stem cell expansion in mouse colonic organoids.

Indexed as

Cell DivisionColonGreen Fluorescent ProteinsHumansProstaglandinsReal-Time Polymerase Chain ReactionStem CellsGreen Fluorescent ProteinsProstaglandins

Identifiers

PMID24336194
PMCPMC3941743
OpenAlexW2162162312

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.