Evidence map›Paper›PMID 16335783›Full record

ArticleMolecular and cellular biochemistry2005

Proteome profiling of human epithelial ovarian cancer cell line TOV-112D.

Jean-Philippe Gagné, Pierre Gagné, Joanna M Hunter, Marie-Eve Bonicalzi, Jean-François Lemay, Isabelle Kelly, Cécile Le Page, Diane Provencher, Anne-Marie Mes-Masson, Amaud Droit and 2 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
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  5. RNA-binding protein KHSRP promotes tumor growth and metastasis in non-small cell lung cancer.Journal of experimental & clinical cancer research : CR · 2019
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  10. Lipocalin2 expressions correlate significantly with tumor differentiation in epithelial ovarian cancer.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2009
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  11. 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

12 authors at 4 institutions in 1 country.

Jean-Philippe GagnéHealth and Environment Unit, Laval University Medical Research Center, CHUQ, Faculty of Medicine, Laval University, Boulevard Laurier, Ste-Foy, Québec, Canada.
Pierre Gagné
Joanna M Hunter
Marie-Eve Bonicalzi
Jean-François Lemay
Isabelle Kelly
Cécile Le Page
Diane Provencher
Anne-Marie Mes-Masson
Amaud Droit
David Bourgais
Guy G Poirier
Université Laval · CAHôpital Notre-Dame · CAWilfrid Laurier University · CACentre Hospitalier de l’Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A proteome profiling of the epithelial ovarian cancer cell line TOV-112D was initiated as a protein expression reference in the study of ovarian cancer. Two complementary proteomic approaches were used in order to maximise protein identification: two-dimensional gel electrophoresis (2DE) protein separation coupled to matrix assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) and one-dimensional gel electrophoresis (1DE) coupled to liquid-chromatography tandem mass spectrometry (LC MS/MS). One hundred and seventy-two proteins have been identified among 288 spots selected on two-dimensional gels and a total of 579 proteins were identified with the 1DE LC MS/MS approach. This proteome profiling covers a wide range of protein expression and identifies several proteins known for their oncogenic properties. Bioinformatics tools were used to mine databases in order to determine whether the identified proteins have previously been implicated in pathways associated with carcinogenesis or cell proliferation. Indeed, several of the proteins have been reported to be specific ovarian cancer markers while others are common to many tumorigenic tissues or proliferating cells. The diversity of proteins found and their association with known oncogenic pathways validate this proteomic approach. The proteome 2D map of the TOV-112D cell line will provide a valuable resource in studies on differential protein expression of human ovarian carcinomas while the 1DE LC MS/MS approach gives a picture of the actual protein profile of the TOV-112D cell line. This work represents one of the most complete ovarian protein expression analysis reports to date and the first comparative study of gene expression profiling and proteomic patterns in ovarian cancer.

Indexed as

Gene Expression ProfilingCell Line, TransformedCell Line, TumorComputational BiologyEpithelial CellsFemaleHumansNeoplasm ProteinsOligonucleotide Array Sequence AnalysisOvarian NeoplasmsPeptide MappingProteomeProteomicsReproducibility of ResultsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTranscription, GeneticNeoplasm ProteinsProteome

Identifiers

PMID16335783
OpenAlexW2068529673

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.