Evidence map›Paper›PMID 22237417›Full record

ArticleGenes and immunity2012

Macrophage-stimulating protein polymorphism rs3197999 is associated with a gain of function: implications for inflammatory bowel disease.

F Häuser, C Deyle, D Berard, C Neukirch, C Glowacki, J K Bickmann, J J Wenzel, K J Lackner, H Rossmann

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Medicina (Kaunas, Lithuania) · 2024
    Article
  4. Article
  5. The Immunogenetics of Autoimmune Cholestasis.Clinics in liver disease · 2016
    Review
  6. Article
  7. Genetics in PSC: what do the "risk genes" teach us?Clinical reviews in allergy & immunology · 2015
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Ron receptor tyrosine kinase signaling as a therapeutic target.Expert opinion on therapeutic targets · 2012
    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

9 authors at 3 institutions in 1 country.

F HäuserInstitute of Clinical Chemistry and Laboratory Medicine, University Medical Centre Mainz, Mainz, Germany.
C Deyle
D Berard
C Neukirch
C Glowacki
J K Bickmann
J J Wenzel
K J Lackner
H Rossmann
Johannes Gutenberg University Mainz · DEInstitute of Medical Microbiology and Hygiene · DEUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crohn's disease and ulcerative colitis, the two main types of inflammatory bowel disease (IBD), were reported to be associated with a variety of genetic polymorphisms. A subset of these polymorphisms was identified in both diseases and only three of them were found in primary sclerosing cholangitis (PSC). rs3197999 (Arg689Cys) located in the MST1 gene is one of the most convincingly replicated IBD/PSC-associated polymorphisms but its functional consequences have not been investigated, yet. We expressed both MST1 gene variants (Arg(689) (MSP(wt)) and Cys(689) (MSP(mut)) in a eukaryotic cell system and compared their stimulatory effects on macrophage-like THP-1 cells. Except for the rate of apoptosis that remained unchanged, MSP(mut) significantly increased the stimulatory effect of MSP (macrophage-stimulating protein) on chemotaxis and proliferation by THP-1 cells, indicating a gain of function associated with the Arg689Cys exchange. A broad set of evidence reported previously suggests that pro-inflammatory changes in macrophage function have a major role in the initiation of the inflammatory process in IBD and PSC. Therefore, the gain of function observed with rs3197999 in MST1 might provide a cellular mechanism for the consistent association of this polymorphism with an increased risk for IBD and PSC.

Indexed as

AnimalsApoptosisCell MovementCell ProliferationChemotaxisCHO CellsCholangitis, SclerosingCricetinaeDNA, ComplementaryHepatocyte Growth FactorHep G2 CellsHumansInflammatory Bowel DiseasesInterferon-gammaMacrophagesMonocytesDNA, ComplementaryHepatocyte Growth FactorInterferon-gammamacrophage stimulating proteinProto-Oncogene ProteinsRecombinant ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID22237417
OpenAlexW1963853720

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.