Evidence map›Paper›PMID 22162229›Full record

ArticleMolecular carcinogenesis2012

Aberrant signaling pathways in pancreatic cancer: a two compartment view.

Angela L McCleary-Wheeler, Robert McWilliams, Martin E Fernandez-Zapico

Abstract read
In one paragraph

Article in Molecular carcinogenesis, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  13. Translational molecular imaging in exocrine pancreatic cancer.European journal of nuclear medicine and molecular imaging · 2018
    Review
  14. Article
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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

3 authors at 2 institutions in 1 country.

Angela L McCleary-WheelerSchulze Center for Novel Therapeutics, Mayo Clinic, Rochester, Minnesota 55905, USA.
Robert McWilliams
Martin E Fernandez-Zapico
Mayo Clinic · USNovel (United States) · US

Funding

Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M. · 2004 to 2018
$32.7M
PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
Mechanism of Pancreatic CarcinogenesisR01CA136526 · NCI · MAYO CLINIC ROCHESTER · PI FERNANDEZ-ZAPICO, MARTIN ERNESTO · 2009 to 2019
$3.0M
Genetic Epidemiology of Young-Onset Pancreatic CancerK07CA116303 · NCI · MAYO CLINIC ROCHESTER · PI MCWILLIAMS, ROBERT R · 2006 to 2010
$656k
NCI NIH HHS CA136526NCI NIH HHS K07 CA116303NCI NIH HHS NCI K07 CA116303NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA136526NIDDK NIH HHS P30 DK084567
6 · The paper itself

Abstract

Pancreatic cancer is a devastating disease with historically limited success in treatment and a poor prognosis. Pancreatic cancer appears to have a progressive pathway of development, initiating from well-described pancreatic intraepithelial neoplasia lesions and concluding with invasive carcinoma. These early lesions have been shown to harbor-specific alterations in signaling pathways that remain throughout this tumorigenesis process. Meanwhile, new alterations occur during this process of disease progression to have a cumulative effect. This series of events not only impacts the epithelial cells comprising the tumor, but they may also affect the surrounding stromal cells. The result is the formation of complex signaling networks of communication between the tumor epithelial cell and the stromal cell compartments to promote a permissive and cooperative environment. This article highlights some of the most common pathway aberrations involved with this disease, and how these may subsequently affect one or both cellular compartments. Consequently, furthering our understanding of these pathways in terms of their function on the tumoral epithelial and stromal compartments may prove to be crucial to the development of targeted and more successful therapies in the future.

Indexed as

AdenocarcinomaCell CommunicationClinical Trials as TopicEpithelial CellsGenes, p16Genes, p53Hedgehog ProteinsHumansMolecular Targeted TherapyPancreatic NeoplasmsProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)ras ProteinsReceptors, NotchSignal TransductionStromal CellsHedgehog ProteinsKRAS protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)ras ProteinsReceptors, NotchTransforming Growth Factor betaWnt Proteins

Identifiers

PMID22162229
PMCPMC3253704
OpenAlexW2145963785

What OpenQuestion holds

Textmetadata
LicenceTDM
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.