Evidence map›Paper›PMID 25347153›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2015

Proteins associated with pancreatic cancer survival in patients with resectable pancreatic ductal adenocarcinoma.

Ru Chen, David W Dawson, Sheng Pan, Niki A Ottenhof, Roeland F de Wilde, Christopher L Wolfgang, Damon H May, David A Crispin, Lisa A Lai, Anna R Lay and 6 more

Open access · greenAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Implications of mHeliyon · 2024
    Article
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  9. Review
  10. Article
  11. Review
  12. Article
  13. Downregulation of Methionine Cycle GenesInternational journal of molecular sciences · 2022
    Article
  14. Review
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  16. Review
  17. Review
  18. Article
  19. Observational
  20. Insulin-Like Growth Factor-1 Receptor Expression and Disease Recurrence and Survival in Patients with Resected Pancreatic Ductal Adenocarcinoma.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    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

16 authors at 9 institutions in 2 countries.

Ru ChenDepartment of Medicine, University of Washington, Seattle, WA, USA.
David W Dawson1] Department of Pathology and Laboratory Medicine, UCLA, Los Angeles, CA, USA [2] Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Sheng PanDepartment of Medicine, University of Washington, Seattle, WA, USA.
Niki A OttenhofDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Roeland F de WildeDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Christopher L WolfgangDepartment of Surgery, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Damon H MayFred Hutchinson Cancer Research Center, Molecular Diagnostics Program, Seattle, WA, USA.
David A CrispinDepartment of Medicine, University of Washington, Seattle, WA, USA.
Lisa A LaiDepartment of Medicine, University of Washington, Seattle, WA, USA.
Anna R LayDepartment of Pathology and Laboratory Medicine, UCLA, Los Angeles, CA, USA.
Meghna WaghrayDepartment of Surgery, University of Michigan, Ann Arbor, MI, USA.
Shouli WangDepartment of Pathology, Soochow University School of Medicine, Suzhou, China.
Martin W McIntoshFred Hutchinson Cancer Research Center, Molecular Diagnostics Program, Seattle, WA, USA.
Diane M SimeoneDepartment of Surgery, University of Michigan, Ann Arbor, MI, USA.
Anirban MaitraDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Teresa A BrentnallDepartment of Medicine, University of Washington, Seattle, WA, USA.
University of Washington · USCancer Research Center · USFred Hutch Cancer Center · USUniversity of Michigan–Ann Arbor · USJohns Hopkins University · USSoochow University · CNThe University of Texas MD Anderson Cancer Center · USUCLA Jonsson Comprehensive Cancer CenterUniversity of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Targeting diet-induced promotion of Kras-initiated pancreatic adenocarcinomaP01CA163200 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PANDOL, STEPHEN J. · 2012 to 2016
$6.2M
Early detection of pancreatic cancer in diabeticsR01CA180949 · NCI · UNIVERSITY OF WASHINGTON · PI CHEN, RU, PAN, SHENG · 2014 to 2018
$2.9M
Protein biomarkers for detection of pancreatic cancerK07CA116296 · NCI · UNIVERSITY OF WASHINGTON · PI CHEN, RU · 2007 to 2011
$650k
Quantitative glycoproteomics for pancreatic cancer studiesK25CA137222 · NCI · UNIVERSITY OF WASHINGTON · PI PAN, SHENG · 2010 to 2014
$612k
Aberrant Glycosylation Signature in Pancreatic CancerR21CA149772 · NCI · UNIVERSITY OF WASHINGTON · PI BRENTNALL, TERESA A, PAN, SHENG · 2011 to 2012
$396k
Pancreatic Juice Biomarker for Pancreatic CancerR21CA161575 · NCI · UNIVERSITY OF WASHINGTON · PI CHEN, RU · 2011 to 2012
$388k
NCI NIH HHS K07 CA116296NCI NIH HHS K07CA116296NCI NIH HHS K25 CA137222NCI NIH HHS K25CA137222NCI NIH HHS P01 CA163200NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA180949NCI NIH HHS R01CA180949NCI NIH HHS R21 CA149772NCI NIH HHS R21CA149772NCI NIH HHS R21 CA161575NCI NIH HHS R21CA161575NIDDK NIH HHS P30 DK041301
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal disease with a dismal prognosis. However, while most patients die within the first year of diagnosis, very rarely, a few patients can survive for >10 years. Better understanding the molecular characteristics of the pancreatic adenocarcinomas from these very-long-term survivors (VLTS) may provide clues for personalized medicine and improve current pancreatic cancer treatment. To extend our previous investigation, we examined the proteomes of individual pancreas tumor tissues from a group of VLTS patients (survival ≥10 years) and short-term survival patients (STS, survival <14 months). With a given analytical sensitivity, the protein profile of each pancreatic tumor tissue was compared to reveal the proteome alterations that may be associated with pancreatic cancer survival. Pathway analysis of the differential proteins identified suggested that MYC, IGF1R and p53 were the top three upstream regulators for the STS-associated proteins, and VEGFA, APOE and TGFβ-1 were the top three upstream regulators for the VLTS-associated proteins. Immunohistochemistry analysis using an independent cohort of 145 PDAC confirmed that the higher abundance of ribosomal protein S8 (RPS8) and prolargin (PRELP) were correlated with STS and VLTS, respectively. Multivariate Cox analysis indicated that 'High-RPS8 and Low-PRELP' was significantly associated with shorter survival time (HR=2.69, 95% CI 1.46-4.92, P=0.001). In addition, galectin-1, a previously identified protein with its abundance aversely associated with pancreatic cancer survival, was further evaluated for its significance in cancer-associated fibroblasts. Knockdown of galectin-1 in pancreatic cancer-associated fibroblasts dramatically reduced cell migration and invasion. The results from our study suggested that PRELP, LGALS1 and RPS8 might be significant prognostic factors, and RPS8 and LGALS1 could be potential therapeutic targets to improve pancreatic cancer survival if further validated.

Indexed as

Survival AnalysisAdenocarcinomaCarcinoma, Pancreatic DuctalCell Line, TumorFemaleHumansMaleMiddle AgedNeoplasm ProteinsPancreatic NeoplasmsProteomicsNeoplasm Proteins

Identifiers

PMID25347153
PMCPMC4281293
OpenAlexW2057594180

What OpenQuestion holds

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Registered trials

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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.