Evidence map›Paper›PMID 25743245›Full record

ArticleCytokine2015

Plasma immune analytes in patients with epithelial ovarian cancer.

Matthew S Block, Matthew J Maurer, Krista Goergen, Kimberly R Kalli, Courtney L Erskine, Marshall D Behrens, Ann L Oberg, Keith L Knutson

Abstract read
In one paragraph

Article in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.2field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  7. Prognostic and Clinical Value of Interleukin 6 and CD45Journal of immunology research · 2020
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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

8 authors at 3 institutions in 1 country.

Matthew S BlockDepartment of Oncology, Mayo Clinic, Rochester, MN, United States; Department of Immunology, Mayo Clinic, Rochester, MN, United States. Electronic address: block.matthew@mayo.edu.
Matthew J MaurerDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, United States.
Krista GoergenDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, United States.
Kimberly R KalliDepartment of Oncology, Mayo Clinic, Rochester, MN, United States.
Courtney L ErskineDepartment of Immunology, Mayo Clinic, Rochester, MN, United States.
Marshall D BehrensDepartment of Immunology, Mayo Clinic, Rochester, MN, United States.
Ann L ObergDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, United States.
Keith L KnutsonVaccine and Gene Therapy Institute, Port Saint Lucie, FL, United States; Department of Immunology, Mayo Clinic, Rochester, MN, United States.
Mayo Clinic · USWinnMed · USMayo Clinic in Arizona · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
NCI NIH HHS CA136393NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA136393
6 · The paper itself

Abstract

objectivesInflammation is a common feature of epithelial ovarian cancer (EOC), and measurement of plasma markers of inflammation might identify candidate markers for use in screening or presurgical evaluation of patients with adnexal masses.

methodsPlasma specimens from cohorts of 100 patients with advanced EOC (AJCC Stage III and IV), 50 patients with early stage EOC (Stage I and II), and 50 patients with benign surgical conditions were assayed for concentrations of multiple cytokines, toll-like receptor agonists, and vascular growth factors via ELISA and electrochemiluminescence. Immune proteins were then analyzed for association with EOC. Differences in plasma protein levels between benign, early, and advanced EOC patient groups were assessed with and without adjustment for plasma cancer antigen 125 (CA-125) levels.

resultsOut of 23 proteins tested, six-including interferon gamma (IFNγ), interleukin 6 (IL-6), IL-8, IL-10, tumor necrosis factor alpha (TNFα), and placental growth factor (PlGF)-were univariately associated with EOC (all p<0.005), and one-IL-6-was associated with early stage EOC (p<0.0001). Heat shock protein 90kDa beta member 1 (HSP90B1, gp96) was associated with EOC and early stage EOC with borderline statistical significance (p=0.039 and p=0.026, respectively). However, when adjusted for (CA-125), only HSP90B1 independently predicted EOC (p=0.008), as well as early stage EOC (p=0.014).

conclusionsMultiple plasma cytokines, including IFNγ, IL-6, IL-8, IL-10, TNFα, PlGF, and HSP90B1 are associated with EOC. Of these, HSP90B1 is associated with EOC independent from the biomarker CA-125.

Indexed as

AdultAgedAged, 80 and overBiomarkersCA-125 AntigenCarcinoma, Ovarian EpithelialCytokinesFemaleHumansInflammationLogistic ModelsMembrane GlycoproteinsMembrane ProteinsMiddle AgedNeoplasms, Glandular and EpithelialOvarian NeoplasmsBiomarkersCA-125 AntigenCytokinesendoplasminMembrane GlycoproteinsMembrane ProteinsMUC16 protein, humanHSP90B1Interleukin 6 (IL-6)Ovarian cancer

Identifiers

PMID25743245
PMCPMC4380743
OpenAlexW2060390227

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.