Evidence map›Paper›PMID 15920164›Full record

ArticleThe American journal of pathology2005

Dual infection with Helicobacter bilis and Helicobacter hepaticus in p-glycoprotein-deficient mdr1a-/- mice results in colitis that progresses to dysplasia.

Lillian Maggio-Price, Helle Bielefeldt-Ohmann, Piper Treuting, Brian M Iritani, Weiping Zeng, Andrea Nicks, Mark Tsang, Donna Shows, Phil Morrissey, Joanne L Viney

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The American journal of pathology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. BioMed research international · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. In Vivo Anti Cancer Potential of Pyrogallol in Murine Model of Colon Cancer.Asian Pacific journal of cancer prevention : APJCP · 2019
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Relationship between intestinal microbiota and colorectal cancer.World journal of gastrointestinal oncology · 2015
    Review
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

10 authors at 3 institutions in 1 country.

Lillian Maggio-PriceDepartment of Comparative Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA. lmprice@u.washington.edu
Helle Bielefeldt-Ohmann
Piper Treuting
Brian M Iritani
Weiping Zeng
Andrea Nicks
Mark Tsang
Donna Shows
Phil Morrissey
Joanne L Viney
Amgen (United States) · USUniversity of Washington · USSeattle University · US

Funding

Control of T Lymphopoiesis and Growth by Mad GenesR01AI053568 · NIAID · UNIVERSITY OF WASHINGTON · PI IRITANI, BRIAN M · 2003 to 2007
$1.5M
NIAID NIH HHS 1R01 AI053568-01NIAID NIH HHS R01 AI053568
6 · The paper itself

Abstract

Patients with inflammatory bowel disease (IBD) are at increased risk for developing high-grade dysplasia and colorectal cancer. Animal IBD models that develop dysplasia and neoplasia may help elucidate the link between inflammation and colorectal cancer. Mdr1a-/- mice lack the membrane efflux pump p-glycoprotein and spontaneously develop IBD that can be modulated by infection with Helicobacter sp: H. bilis accelerates development of colitis while H. hepaticus delays disease. In this study, we determined if H. hepaticus infection could prevent H. bilis-induced colitis. Unexpectedly, a proportion of dual-infected mdr1a-/- mice showed IBD with foci of low- to high-grade dysplasia. A group of dual-infected mdr1a-/- animals were maintained long term (39 weeks) by intermittent feeding of medicated wafers to model chronic and relapsing disease. These mice showed a higher frequency of high-grade crypt dysplasia, including invasive adenocarcinoma, possibly because H. hepaticus, in delaying the development of colitis, allows time for transformation of epithelial cells. Colonic epithelial preparations from co-infected mice showed increased expression of c-myc (5- to 12-fold) and interleukin-1alpha/beta (600-fold) by real-time polymerase chain reaction relative to uninfected wild-type and mdr1a-/- animals. This animal model may have particular relevance to human IBD and colorectal cancer because certain human MDR1 polymorphisms have been linked to ulcerative colitis and increased risk for colorectal cancer.

Indexed as

AdenocarcinomaAnimalsATP Binding Cassette Transporter, Subfamily B, Member 1ColitisDisease Models, AnimalHelicobacter hepaticusHelicobacter InfectionsImmunohistochemistryInterleukin-1Intestinal NeoplasmsMiceMice, Mutant StrainsPrecancerous ConditionsProto-Oncogene Proteins c-mycReverse Transcriptase Polymerase Chain ReactionATP Binding Cassette Transporter, Subfamily B, Member 1Interleukin-1Myc protein, mouseProto-Oncogene Proteins c-myc

Identifiers

PMID15920164
PMCPMC1602406
OpenAlexW1984076434

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.