Evidence map›Paper›PMID 34449791›Full record

ArticlePloS one2021

The blood transcriptome prior to ovarian cancer diagnosis: A case-control study in the NOWAC postgenome cohort.

Mie Jareid, Igor Snapkov, Marit Holden, Lill-Tove Rasmussen Busund, Eiliv Lund, Therese Haugdahl Nøst

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

6 authors at 4 institutions in 1 country.

Mie JareidFaculty of Health Sciences, Department of Community Medicine, UiT - The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0003-3192-7311
Igor SnapkovDepartment of Immunology, Oslo University Hospital Rikshospitalet and University of Oslo, Oslo, Norway.
Marit HoldenNorwegian Computing Center, Oslo, Norway.
Lill-Tove Rasmussen BusundFaculty of Health Sciences, Department of Medical Biology, UiT - The Arctic University of Norway, Tromsø, Norway.
Eiliv LundFaculty of Health Sciences, Department of Community Medicine, UiT - The Arctic University of Norway, Tromsø, Norway.
Therese Haugdahl NøstFaculty of Health Sciences, Department of Community Medicine, UiT - The Arctic University of Norway, Tromsø, Norway.
UiT The Arctic University of Norway · NOCancer Registry of Norway · NONorwegian Computing Center · NOOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) has a 5-year relative survival of 50%, partly because markers of early-stage disease are not available in current clinical diagnostics. The aim of the present study was to investigate whether EOC is associated with transcriptional profiles in blood collected up to 7 years before diagnosis. For this, we used RNA-stabilized whole blood, which contains circulating immune cells, from a sample of EOC cases from the population-based Norwegian Women and Cancer (NOWAC) postgenome cohort. We explored case-control differences in gene expression in all EOC (66 case-control pairs), as well as associations between gene expression and metastatic EOC (56 pairs), serous EOC (45 pairs, 44 of which were metastatic), and interval from blood sample collection to diagnosis (≤3 or >3 years; 34 and 31 pairs, respectively). Lastly, we assessed differential expression of genes associated with EOC in published functional genomics studies that used blood samples collected from newly diagnosed women. After adjustment for multiple testing, this nested case-control study revealed no significant case-control differences in gene expression in all EOC (false discovery rate q>0.96). With the exception of a few probes, the log2 fold change values obtained in gene-wise linear models were below ±0.2. P-values were lowest in analyses of metastatic EOC (80% of which were serous EOC). No common transcriptional profile was indicated by interval to diagnosis; when comparing the 100 genes with the lowest p-values in gene-wise tests in samples collected ≤3 and >3 years before EOC diagnosis, no overlap in these genes was observed. Among 86 genes linked to ovarian cancer in previous publications, our data contained expression values for 42, and of these, tests of LIME1, GPR162, STAB1, and SKAP1, resulted in unadjusted p<0.05. Although limited by sample size, our findings indicated less variation in blood gene expression between women with similar tumor characteristics.

Indexed as

Adaptor Proteins, Vesicular TransportCell Adhesion Molecules, NeuronalCohort StudiesCystadenocarcinoma, SerousFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoplasm MetastasisNeoplasm ProteinsNorwayOvarian NeoplasmsPhosphoproteinsReceptors, G-Protein-CoupledReceptors, Lymphocyte HomingTranscriptomeAdaptor Proteins, Vesicular TransportCell Adhesion Molecules, NeuronalGpr162 protein, humanLIME1 protein, humanNeoplasm ProteinsPhosphoproteinsReceptors, G-Protein-CoupledReceptors, Lymphocyte HomingSKAP1 protein, humanSTAB1 protein, human

Identifiers

PMID34449791
PMCPMC8396762
OpenAlexW3195987413

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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.