Evidence map›Paper›PMID 22194851›Full record

ArticlePloS one2011

Copy number variation analysis of matched ovarian primary tumors and peritoneal metastasis.

Joel A Malek, Eliane Mery, Yasmin A Mahmoud, Eman K Al-Azwani, Laurence Roger, Ruby Huang, Eva Jouve, Raphael Lis, Jean-Paul Thiery, Denis Querleu and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  20. Evaluation of a hypoxia regulated gene panel in ovarian cancer.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2015
    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

11 authors at 5 institutions in 5 countries.

Joel A MalekGenomics Core, Weill Cornell Medical College in Qatar, Education City, Qatar Foundation, Doha, Qatar.
Eliane Mery
Yasmin A Mahmoud
Eman K Al-Azwani
Laurence Roger
Ruby Huang
Eva Jouve
Raphael Lis
Jean-Paul Thiery
Denis Querleu
Arash Rafii
Institut Claudius Regaud · FRWeill Cornell Medical College in Qatar · QACornell University · USAgency for Science, Technology and Research · SGNational University of Singapore · SG

Funding

Southern California Clinical and Translational Science InstituteUL1TR000130 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2012 to 2015
$36.0M
NCATS NIH HHS UL1 TR000130
6 · The paper itself

Abstract

Ovarian cancer is the most deadly gynecological cancer. The high rate of mortality is due to the large tumor burden with extensive metastatic lesion of the abdominal cavity. Despite initial chemosensitivity and improved surgical procedures, abdominal recurrence remains an issue and results in patients' poor prognosis. Transcriptomic and genetic studies have revealed significant genome pathologies in the primary tumors and yielded important information regarding carcinogenesis. There are, however, few studies on genetic alterations and their consequences in peritoneal metastatic tumors when compared to their matched ovarian primary tumors. We used high-density SNP arrays to investigate copy number variations in matched primary and metastatic ovarian cancer from 9 patients. Here we show that copy number variations acquired by ovarian tumors are significantly different between matched primary and metastatic tumors and these are likely due to different functional requirements. We show that these copy number variations clearly differentially affect specific pathways including the JAK/STAT and cytokine signaling pathways. While many have shown complex involvement of cytokines in the ovarian cancer environment we provide evidence that ovarian tumors have specific copy number variation differences in many of these genes.

Indexed as

AgedChemokines, CCDNA Copy Number VariationsFemaleGenes, NeoplasmGenome, HumanHumansJanus KinasesOvarian NeoplasmsPeritoneal NeoplasmsReceptors, ChemokineSTAT Transcription FactorsTumor Cells, CulturedChemokines, CCJanus KinasesReceptors, ChemokineSTAT Transcription Factors

Identifiers

PMID22194851
PMCPMC3237432
OpenAlexW2050216612

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.