Evidence map›Paper›PMID 15632002›Full record

ArticleThe American journal of pathology2005

Expression of S100P and its novel binding partner S100PBPR in early pancreatic cancer.

Sally E Dowen, Tatjana Crnogorac-Jurcevic, Rathi Gangeswaran, Mikkel Hansen, Jyrki J Eloranta, Vipul Bhakta, Teresa A Brentnall, Jutta Lüttges, Gunther Klöppel, Nick R Lemoine

Open access · greenAbstract read
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 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.4field-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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 131 citations in OpenAlex.

  1. Diagnostic value of S100P for pancreatic cancer: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  2. Trial
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  10. Case report: 16-yr life history and genomic evolution of an ERCold Spring Harbor molecular case studies · 2020
    Article
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  14. Review
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  16. Article
  17. The life and works of S100P - from conception to cancer.American journal of cancer research · 2016
    Review
  18. Role of S100 Proteins in Colorectal Carcinogenesis.Gastroenterology research and practice · 2016
    Review
  19. Article
  20. 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

10 authors at 3 institutions in 3 countries.

Sally E DowenMolecular Oncology Unit, Barts and The London School of Medicine and Dentistry, John Vane Science Centre, Charterhouse Square, London, EC1M 6BQ, UK.
Tatjana Crnogorac-Jurcevic
Rathi Gangeswaran
Mikkel Hansen
Jyrki J Eloranta
Vipul Bhakta
Teresa A Brentnall
Jutta Lüttges
Gunther Klöppel
Nick R Lemoine
Queen Mary University of London · GBKiel University · DEUniversity of Washington Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

S100P is a member of the S100 family of calcium-binding proteins and there have been several recent reports of its overexpression in pancreatic ductal adenocarcinoma (PDAC). We have used Far Western screening and in vitro interaction assays to identify and confirm a novel target protein for S100P. We have named this protein S100PBPR, and shown that its interaction with S100P is dependent on Ca(2+) or Mg(2+). S100PBPR was found to localize to cell nuclei where S100P is also present, and the two proteins co-immunoprecipitate. By in situ hybridization, S100PBPR transcript was found in islet cells but not duct cells of the healthy pancreas. Both S100P and S100PBPR were detected by quantitative real-time polymerase chain reaction in pancreatic intraepithelial neoplasia (PanIN) and PDAC samples, and in situ hybridization revealed the presence of S100PBPR transcript in malignant PDAC cells. These data suggest that an interaction between S100P and S100PBPR may be involved in early pancreatic cancer. S100P was further investigated in PanIN lesions and immunohistochemical analysis showed its expression to correlate significantly with increasing grade of PanINs, being found as early as PanIN-1 with more prevalent expression in PanIN-2 and -3. These data suggest that S100P can be added to the genetic progression model for PDAC.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinomaBase SequenceCalciumCalcium-Binding ProteinsCarrier ProteinsCloning, MolecularDisease ProgressionDNA PrimersHumansIn Situ HybridizationMagnesiumNeoplasm ProteinsNuclear ProteinsPancreatic NeoplasmsPolymerase Chain ReactionCalciumCalcium-Binding ProteinsCarrier ProteinsDNA PrimersMagnesiumNeoplasm ProteinsNuclear ProteinsRNA, MessengerS100PBP protein, humanS100P protein, human

Identifiers

PMID15632002
PMCPMC1602285
OpenAlexW2040655951

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.