Evidence map›Paper›PMID 18258927›Full record

ReviewThe Journal of molecular diagnostics : JMD2008

Molecular genetics of pancreatic ductal adenocarcinomas and recent implications for translational efforts.

Georg Feldmann, Anirban Maitra

Abstract readReview
In one paragraph

Review in The Journal of molecular diagnostics : JMD, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
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  4. Review
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  11. Article
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  15. Article
  16. Chemoprevention of pancreatic cancer-one step closer.Langenbeck's archives of surgery · 2012
    Review
  17. The molecular and cellular heterogeneity of pancreatic ductal adenocarcinoma.Nature reviews. Gastroenterology & hepatology · 2011
    Review
  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

2 authors.

Georg FeldmannThe Sol Goldman Pancreatic Cancer Research Center, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA. gfeldma4@jhmi.edu
Anirban Maitra

Funding

Hedgehog Inhibitors in Pancreas CancerR01CA113669 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAITRA, ANIRBAN · 2005 to 2014
$3.1M
Hedgehog signaling in pancreatic neoplasiaR21DK072532 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI MAITRA, ANIRBAN · 2005 to 2006
$443k
NCI NIH HHS R01 CA113669NCI NIH HHS R01CA113669NIDDK NIH HHS R21 DK072532NIDDK NIH HHS R21DK072532
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (ie, pancreatic cancer) is among the most devastating of human malignancies. It is commonly diagnosed at advanced, already metastatic, and, hence, incurable stages. Despite extensive research efforts in recent decades, pancreatic cancer remains resistant to almost all clinically available therapy regimens. Recent advances in our understanding of the underlying pathophysiology and molecular biology have opened up avenues for the development of novel diagnostic and therapeutic strategies, some of which have shown highly promising preclinical results and are currently being translated into clinical application. Here in we present a review of recent literature on the molecular genetics of pancreatic cancer and emphasize clinical implications for the development of novel diagnostic and therapeutic approaches.

Indexed as

AdenocarcinomaAnimalsCarcinoma, Pancreatic DuctalEpigenesis, GeneticGene Expression ProfilingHumansProteomicsTelomere

Identifiers

PMID18258927
PMCPMC2259464

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.