Evidence map›Paper›PMID 30111871›Full record

ArticleBritish journal of cancer2018

BRCA1 and BRCA2 mRNA-expression prove to be of clinical impact in ovarian cancer.

Irina Tsibulak, Verena Wieser, Christine Degasper, Giridhar Shivalingaiah, Sören Wenzel, Susanne Sprung, Sigurd F Lax, Christian Marth, Heidelinde Fiegl, Alain G Zeimet

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. The Effects ofCells · 2026
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  10. DNA Repair Pathway in Ovarian Cancer Patients Treated with HIPEC.International journal of molecular sciences · 2023
    Article
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  13. Review
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  17. Nucleic acid vaccination strategies for ovarian cancer.Frontiers in bioengineering and biotechnology · 2022
    Review
  18. Review
  19. 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

10 authors at 3 institutions in 1 country.

Irina TsibulakDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria.
Verena WieserDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria.
Christine DegasperDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria.
Giridhar ShivalingaiahDivision of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.
Sören WenzelDivision of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.
Susanne SprungInstitute of Pathology, Medical University of Innsbruck, Innsbruck, Austria.
Sigurd F LaxDepartment of Pathology, Hospital Graz Süd-West, Academic Teaching Hospital of the Medical University Graz, Graz, Austria.
Christian MarthDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria.
Heidelinde FieglDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria. Heidelinde.Fiegl@i-med.ac.at.
Alain G ZeimetDepartment of Obstetrics and Gynecology, Medical University of Innsbruck, Innsbruck, Austria. Alain.Zeimet@i-med.ac.at.
Innsbruck Medical University · ATGraz University Hospital · ATUniversität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutations in BRCA1 and BRCA2 are associated with better survival in ovarian cancer (OC) patients due to a better response to platinum-based chemotherapy. However, the impact of the BRCA1/2 mRNA-expression is not well characterized in OC. PATIENTS AND

methodsWe investigated BRCA1/2 mRNA-expression in 12 non-neoplastic fallopian tubes and 201 epithelial OCs in relation to their clinical characteristics.

resultsWe found higher BRCA1/2 mRNA-expression in OCs compared to controls (P = 0.011, P < 0.001, respectively). BRCA1 mutated OCs exhibited lower BRCA1 (P = 0.014) but higher BRCA2 mRNA-expression (P = 0.001). Low BRCA1-expression was associated with favorable overall survival (OS) (P = 0.012) and low BRCA2-expression with better progression-free survival (PFS) and OS (P = 0.004, P = 0.001, respectively). A subgroup-analysis showed that this effect was confined only to the BRCA1-wildtype cancers. Cox-regression confirmed the prognostic significance of BRCA1-expression for OS (P = 0.028). Independency of the prognostic value of BRCA2-expression for PFS (P = 0.045) and OS (P = 0.015) was restricted to high-grade serous OCs. Fully platinum-sensitivity was characterized by lower BRCA1/2 mRNA-expression in BRCA1-wildtype cancers in comparison to platinum-refractory OC.

conclusionOur findings may reflect higher platinum-sensitivity due to reduced capacity of DNA damage repair in tissues with low BRCA1/2-expression. In this context, especially in BRCA-wildtype cancers both parameters could also be potential predictors for PARP-sensitivity.

Indexed as

Up-RegulationAdultAgedAged, 80 and overBRCA1 ProteinBRCA2 ProteinCarcinoma, Ovarian EpithelialCase-Control StudiesCytoreduction Surgical ProceduresDisease-Free SurvivalFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMiddle AgedMutationBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanPlatinum

Identifiers

PMID30111871
PMCPMC6173779
OpenAlexW2885708852

What OpenQuestion holds

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LicenceCC BY
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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.