Evidence map›Paper›PMID 23798558›Full record

ArticleMolecular & cellular proteomics : MCP2013

Laminin, gamma 2 (LAMC2): a promising new putative pancreatic cancer biomarker identified by proteomic analysis of pancreatic adenocarcinoma tissues.

Hari Kosanam, Ioannis Prassas, Caitlin C Chrystoja, Ireena Soleas, Alison Chan, Apostolos Dimitromanolakis, Ivan M Blasutig, Felix Rückert, Robert Gruetzmann, Christian Pilarsky and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
5.8field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 121 citations in OpenAlex.

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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

13 authors at 7 institutions in 4 countries.

Hari KosanamDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada;
Ioannis Prassas
Caitlin C Chrystoja
Ireena Soleas
Alison Chan
Apostolos Dimitromanolakis
Ivan M Blasutig
Felix Rückert
Robert Gruetzmann
Christian Pilarsky
Masato Maekawa
Randall Brand
Eleftherios P Diamandis
University of Toronto · CALunenfeld-Tanenbaum Research Institute · CAUniversity Hospital Carl Gustav Carus · DEHamamatsu University School of Medicine · JPMount Sinai Hospital · CAUniversity Medical Centre Mannheim · DEUniversity of Pittsburgh Medical Center · US

Funding

An integrated systems biology approach for ovarian cancer biomarker discoveryU01CA152755 · NCI · SINAI HEALTH SYSTEM · PI DIAMANDIS, ELEFTHERIOS P · 2010 to 2015
$1.4M
NCI NIH HHS SU01CA152755NCI NIH HHS U01 CA152755
6 · The paper itself

Abstract

In pancreatic cancer, the incidence and mortality curves coincide. One major reason for this high mortality rate in pancreatic ductal adenocarcinoma (PDAC) patients is the dearth of effective diagnostic, prognostic, and disease-monitoring biomarkers. Unfortunately, existing tumor markers, as well as current imaging modalities, are not sufficiently sensitive and/or specific for early-stage diagnosis. There is, therefore, an urgent need for improved serum markers of the disease. Herein, we performed Orbitrap® mass spectrometry proteomic analysis of four PDAC tissues and their adjacent benign tissues and identified a total of 2190 nonredundant proteins. Sixteen promising candidates were selected for further scrutiny using a systematic scoring algorithm. Our preliminary serum verification of the top four candidates (DSP, LAMC2, GP73, and DSG2) in 20 patients diagnosed with pancreatic cancer and 20 with benign pancreatic cysts, showed a significant (p < 0.05) elevation of LAMC2 in pancreatic cancer serum. Extensive validation of LAMC2 in healthy, benign, and PDAC sera from geographically diverse cohorts (n = 425) (Japan, Europe, and USA) demonstrated a significant increase in levels in early-stage PDAC compared with benign diseases. The sensitivity of LAMC2 was comparable to CA19.9 in all data sets, with an AUC value greater than 0.85 in discriminating healthy patients from early-stage PDAC patients. LAMC2 exhibited diagnostic complementarity with CA19.9 by showing significant (p < 0.001 in two out of three cohorts) elevation in PDAC patients with clinically low CA19.9 levels.

Indexed as

AgedBiomarkers, TumorCarcinoma, Pancreatic DuctalFemaleHumansLamininMaleMiddle AgedPancreatic NeoplasmsProteomicsBiomarkers, TumorLAMC2 protein, humanLaminin

Identifiers

PMID23798558
PMCPMC3790293
OpenAlexW2117331236

What OpenQuestion holds

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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.