Evidence map›Paper›PMID 24548099›Full record

ArticleJournal of gastroenterology and hepatology2014

Osteopontin splice variant as a potential marker for metastatic disease in pancreatic adenocarcinoma.

Ali A Siddiqui, Elizabeth Jones, Darren Andrade, Apeksha Shah, Thomas E Kowalski, David E Loren, Galina Chipitsyna, Hwyda A Arafat

Abstract read
In one paragraph

Article in Journal of gastroenterology and hepatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Human osteopontin: Potential clinical applications in cancer (Review).International journal of molecular medicine · 2017
    Review
  5. Article
  6. Article
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  8. Osteopontin (OPN) isoforms, diabetes, obesity, and cancer; what is one got to do with the other? A new role for OPN.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2015
    Article
  9. 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

8 authors at 1 institution in 1 country.

Ali A SiddiquiDepartment of Internal Medicine, Division of Gastroenterology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Elizabeth Jones
Darren Andrade
Apeksha Shah
Thomas E Kowalski
David E Loren
Galina Chipitsyna
Hwyda A Arafat
Thomas Jefferson University · US

Funding

Nicotine in Pancreatic Cancer: Molecular MechanismsR21CA133753 · NCI · THOMAS JEFFERSON UNIVERSITY · PI ARAFAT, HWYDA A · 2008 to 2009
$396k
NCI NIH HHS 1R21 CA133753-02NCI NIH HHS R21 CA133753
6 · The paper itself

Abstract

BACKGROUND AND

aimOsteopontin (OPN) is a phosphoprotein that activates pathways that induce cancer cell survival and metastasis. Our aim was to examine the expression pattern of OPN splice variants a, b, and c in fine-needle aspirates and to determine their correlation with stage-adjusted pancreatic ductal adenocarcinoma (PDA) survival.

methodsEndoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) was performed in patients with solid pancreatic masses. The tissue was collected and analyzed for the expression of OPN isoforms by reverse transcription-polymerase chain reaction. Survival curves of stages and overexpression of OPN splice variants (a, b, c) were estimated according to the Kaplan-Meier and the log-rank test.

resultsEUS-FNA was performed in 46 patients with solid pancreatic lesions (40 PDA and 6 chronic pancreatitis). OPNa was highly expressed in 39/40 (98%), OPNb in 24/40 (60%), while OPNc was present in 10/40 (25%) of PDA samples. The median survival was lower in patients whose fine-needle aspiration (FNA) samples expressed OPNb than those without (406 days vs 749 days, P = 0.049). There was no significant difference in survival in patients with OPNc. Cox proportional hazard model demonstrated that OPNb expression had a trend toward decrease overall survival (P = 0.06), with these patients having a hazard of death three times higher than those without. OPNc was found to significantly correlate with metastatic disease (P = 0.009) in PDA patients.

conclusionsOur data show for the first time that in FNA samples, there is a strong association between OPNc and presence of metastasis in PDA, and OPNb and poor survival.

Indexed as

Gene ExpressionGenetic Association StudiesGenetic VariationAdenocarcinomaAdultAgedAged, 80 and overBiomarkers, TumorBiopsy, Fine-NeedleEndosonographyFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm MetastasisBiomarkers, TumorOsteopontinProtein Isoformscytologyfine-needle aspiratesosteopontinpancreatic cancer

Identifiers

PMID24548099
PMCPMC4465289
OpenAlexW1766043459

What OpenQuestion holds

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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.