Evidence map›Paper›PMID 23249167›Full record

ArticleJournal of proteome research2013

Chromosome 19 annotations with disease speciation: a first report from the Global Research Consortium.

Carol L Nilsson, Frode Berven, Frode Selheim, Huiling Liu, Joseph R Moskal, Roger A Kroes, Erik P Sulman, Charles A Conrad, Frederick F Lang, Per E Andrén and 21 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

31 authors.

Carol L NilssonDepartment of Pharmacology and Toxicology, UTMB Cancer Center, University of Texas Medical Branch, Galveston, Texas 77555, United States.
Frode Berven
Frode Selheim
Huiling Liu
Joseph R Moskal
Roger A Kroes
Erik P Sulman
Charles A Conrad
Frederick F Lang
Per E Andrén
Anna Nilsson
Elisabet Carlsohn
Hans Lilja
Johan Malm
David Fenyö
Devipriya Subramaniyam
Xiangdong Wang
Maria Gonzales-Gonzales
Noelia Dasilva
Paula Diez
Manuel Fuentes
Ákos Végvári
Karin Sjödin
Charlotte Welinder
Thomas Laurell
Thomas E Fehniger
Henrik Lindberg
Melinda Rezeli
Goutham Edula
Sophia Hober
György Marko-Varga

Funding

SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Yu Chen, MICHAEL J MORRIS · 2001 to 2026
$63.0M
Prospective validation of a multi-marker prostate cancer prediction modelR01CA160816 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BOORJIAN, STEPHEN, COOPERBERG, MATTHEW R · 2012 to 2015
$1.9M
Long-term prediction of prostate cancer death from kallikreins measured in bloodR33CA127768 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LILJA, HANS GÖSTA · 2010 to 2011
$692k
NCI NIH HHS P50 CA092629NCI NIH HHS P50-CA92629NCI NIH HHS R01 CA160816NCI NIH HHS R01CA160816NCI NIH HHS R33 CA127768NCI NIH HHS R33 CA 127768-03
6 · The paper itself

Abstract

A first research development progress report of the Chromosome 19 Consortium with members from Sweden, Norway, Spain, United States, China and India, a part of the Chromosome-centric Human Proteome Project (C-HPP) global initiative, is presented ( http://www.c-hpp.org ). From the chromosome 19 peptide-targeted library constituting 6159 peptides, a pilot study was conducted using a subset with 125 isotope-labeled peptides. We applied an annotation strategy with triple quadrupole, ESI-Qtrap, and MALDI mass spectrometry platforms, comparing the quality of data within and in between these instrumental set-ups. LC-MS conditions were outlined by multiplex assay developments, followed by MRM assay developments. SRM was applied to biobank samples, quantifying kallikrein 3 (prostate specific antigen) in plasma from prostate cancer patients. The antibody production has been initiated for more than 1200 genes from the entire chromosome 19, and the progress developments are presented. We developed a dedicated transcript microarray to serve as the mRNA identifier by screening cancer cell lines. NAPPA protein arrays were built to align with the transcript data with the Chromosome 19 NAPPA chip, dedicated to 90 proteins, as the first development delivery. We have introduced an IT-infrastructure utilizing a LIMS system that serves as the key interface for the research teams to share and explore data generated within the project. The cross-site data repository will form the basis for sample processing, including biological samples as well as patient samples from national Biobanks.

Indexed as

Chromosomes, Human, Pair 19Genome, HumanProteomeRNA, MessengerDatabases, ProteinGene ExpressionHumansMass SpectrometryProtein Array AnalysisTranscriptomeProteomeRNA, Messenger

Identifiers

PMID23249167
PMCPMC3539432

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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.