Evidence map›Paper›PMID 17415382›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2007

Upregulation and redistribution of integrin alpha6beta4 expression occurs at an early stage in pancreatic adenocarcinoma progression.

Zobeida Cruz-Monserrate, Suimin Qiu, B Mark Evers, Kathleen L O'Connor

Abstract read
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

29 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
  2. Integrin α6 Targeted Tumor Theranostics.Phenomics (Cham, Switzerland) · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Immunomagnetic microscopy of tumor tissues using quantum sensors in diamond.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Emerging cancer-specific therapeutic aptamers.Current opinion in oncology · 2017
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  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

4 authors at 1 institution in 1 country.

Zobeida Cruz-MonserrateSealy Center for Cancer Cell Biology, University of Texas Medical Branch, Galveston, TX 77555-0525, USA.
Suimin Qiu
B Mark Evers
Kathleen L O'Connor
The University of Texas Medical Branch at Galveston · US

Funding

Pancreatic Intergin Contribution to Peerineural InvasionR21CA102125 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI O'CONNOR, KATHLEEN L · 2003 to 2004
$227k
Minority Predoctoral Fellowship ProgramF31CA106201 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CRUZ-MONSERRATE, ZOBEIDA · 2003 to 2006
$109k
NCI NIH HHS F31 CA106201NCI NIH HHS R21 CA102125NCI NIH HHS R21-CA102125
6 · The paper itself

Abstract

Pancreatic adenocarcinomas are highly invasive cancers for reasons that are currently unclear. Here we sought to determine if the proinvasive integrin alpha6beta4 may be related to pancreatic adenocarcinoma tumor progression. Expression of integrin alpha6beta4 was analyzed via immunohistochemistry for the beta4 subunit in normal pancreas, pancreatic intraepithelial neoplasia (PanIN) lesions, pancreatic adenocarcinomas and chronic pancreatitis. In normal pancreatic ducts, integrin alpha6beta4 was noted only at the cell's basal interface with the basement membrane. In pancreatic adenocarcinomas, 92% (104/113) demonstrated overexpression of integrin alpha6beta4 and altered localization to the cytoplasm and membranous regions. This pattern of expression was observed in all PanIN lesions as early as PanIN-1A, and was evident in lesions that were juxtapositioned to normal epithelium. In contrast, 93% (13/14) of chronic pancreatitis samples resembled the staining pattern of normal pancreas. When cancer was present in areas of chronic pancreatitis, this altered expression of alpha6beta4 integrin identified the cancer. We conclude that integrin alpha6beta4 is expressed only on the basal surface of ductal cells in normal pancreas and chronic pancreatitis. During pancreatic adenocarcinoma progression, the alpha6beta4 integrin is dramatically overexpressed and displays altered localization at the earliest stages of PanIN, thus representing an early event in pancreatic adenocarcinoma progression.

Indexed as

AdenocarcinomaBiomarkers, TumorCarcinoma in SituHumansImmunohistochemistryIntegrin alpha6beta4PancreasPancreatic DuctsPancreatic NeoplasmsPancreatitis, ChronicUp-RegulationBiomarkers, TumorIntegrin alpha6beta4

Identifiers

PMID17415382
PMCPMC4697742
OpenAlexW2013466786

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.