Evidence map›Paper›PMID 30287916›Full record

ArticleBritish journal of cancer2018

Kallikrein-related peptidases 4, 5, 6 and 7 regulate tumour-associated factors in serous ovarian cancer.

Ping Wang, Viktor Magdolen, Christof Seidl, Julia Dorn, Enken Drecoll, Matthias Kotzsch, Feng Yang, Manfred Schmitt, Oliver Schilling, Anja Rockstroh and 2 more

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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

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  17. New Predictive Biomarkers for Ovarian Cancer.Diagnostics (Basel, Switzerland) · 2021
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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 2 countries.

Ping WangDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Viktor MagdolenDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Christof SeidlDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Julia DornDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Enken DrecollDepartment of Pathology, Technical University of Munich, Munich, Germany.
Matthias KotzschMedizinisches Labor Ostsachsen, Dresden, Germany.
Feng YangDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Manfred SchmittDepartment of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Oliver SchillingInstitute of Molecular Medicine and Cell Research, University of Freiburg, Freiburg, Germany.
Anja RockstrohAustralian Prostate Cancer Research Centre-Queensland, Translational Research Institute, Brisbane, QLD, Australia.
Judith Ann ClementsAustralian Prostate Cancer Research Centre-Queensland, Translational Research Institute, Brisbane, QLD, Australia.
Daniela LoessnerInstitute of Health and Biomedical Innovation, Queensland University of Technology (QUT), Brisbane, QLD, Australia. d.loessner@qmul.ac.uk.
Technical University of Munich · DEQueensland University of Technology · AULabor Pachmann · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTissue kallikrein-related peptidases 4, 5, 6 and 7 (KLK4-7) strongly increase the malignancy of ovarian cancer cells. Deciphering their downstream effectors, we aimed at finding new potential prognostic biomarkers and treatment targets for ovarian cancer patients. KLK4-7-transfected (OV-KLK4-7) and vector-control OV-MZ-6 (OV-VC) ovarian cancer cells were established to select differentially regulated factors.

methodsWith three independent approaches, PCR arrays, genome-wide microarray and proteome analyses, we identified 10 candidates (MSN, KRT19, COL5A2, COL1A2, BMP5, F10, KRT7, JUNB, BMP4, MMP1). To determine differential protein expression, we performed western blot analyses, immunofluorescence and immunohistochemistry for four candidates (MSN, KRT19, KRT7, JUNB) in cells, tumour xenograft and patient-derived tissues.

resultsWe demonstrated that KLK4-7 clearly regulates expression of MSN, KRT19, KRT7 and JUNB at the mRNA and protein levels in ovarian cancer cells and tissues. Protein expression of the top-upregulated effectors, MSN and KRT19, was investigated by immunohistochemistry in patients afflicted with serous ovarian cancer and related to KLK4-7 immunoexpression. Significant positive associations were found for KRT19/KLK4, KRT19/KLK5 and MSN/KLK7.

conclusionThese findings imply that KLK4-7 exert key modulatory effects on other cancer-related genes and proteins in ovarian cancer. These downstream effectors of KLK4-7, MSN and KRT19 may represent important therapeutic targets in serous ovarian cancer.

Indexed as

Gene Regulatory NetworksBiomarkers, TumorCell Line, TumorCystadenocarcinoma, SerousFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansKallikreinsOvarian NeoplasmsPrognosisProteomicsBiomarkers, Tumorkallikrein 4KallikreinsKLK5 protein, humanKLK6 protein, humanKLK7 protein, human

Identifiers

PMID30287916
PMCPMC6189062
OpenAlexW2895721782

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.