Evidence map›Paper›PMID 30811511›Full record

ArticlePloS one2019

Characterization of kallikrein-related peptidase 4 (KLK4) mRNA expression in tumor tissue of advanced high-grade serous ovarian cancer patients.

Weiwei Gong, Yueyang Liu, Christof Seidl, Tobias Dreyer, Enken Drecoll, Matthias Kotzsch, Holger Bronger, Julia Dorn, Viktor Magdolen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Unveiling Biological Age: A New Frontier in Predicting Outcomes in Chronic Lung Disease.American journal of respiratory and critical care medicine · 2024
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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

9 authors at 2 institutions in 1 country.

Weiwei GongClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Yueyang LiuClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Christof SeidlClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Tobias DreyerClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Enken DrecollInstitute of Pathology, Technical University of Munich, Munich, Germany.
Matthias KotzschMedizinisches Labor Ostsachsen, Dresden, Germany.
Holger BrongerClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Julia DornClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
Viktor MagdolenClinical Research Unit, Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.ORCID 0000-0003-0167-793X
Technical University of Munich · DELabor Pachmann · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of several members of the kallikrein-related peptidase (KLK) family, including KLK4, has been reported in ovarian cancer tissue, consistent with the fact that elevated levels of KLK protein are often also found in serum and in effusion fluids of ovarian cancer patients. In the present study, we quantitatively analyzed KLK4 tumor tissue mRNA expression levels in a homogeneous cohort including 138 patients of advanced high-grade serous ovarian cancer (FIGO stage III/IV). Age as well as ascites fluid volume were found to be significantly associated with KLK4 mRNA expression levels. In univariate Cox regression analysis, the clinical factors residual tumor mass and ascites fluid volume represented univariate predictors for both overall survival (OS) and progression-free survival (PFS). Furthermore, elevated KLK4 mRNA expression levels were significantly linked with reduced OS (p = 0.001), but not with PFS. The results concerning the association of KLK4 mRNA expression with OS were validated in a publicly available Affymetrix-based mRNA data set from The Cancer Genome Atlas (n = 252) applying the Kaplan-Meier Plotter tool (p = 0.047). In multivariable analyses, elevated KLK4 mRNA values turned out as an additional, independent predictive marker for shortened OS (p = 0.006), whereas residual tumor mass, but not ascites fluid volume, remained an independent indicator for both OS and PFS (p < 0.001 and p = 0.002, respectively). The results of the present study, obtained in a well-defined, homogenous cohort of patients afflicted with advanced high-grade serous ovarian cancer, are in line with previous reports describing high KLK4 levels as an unfavorable marker in ovarian cancer patients.

Indexed as

Up-RegulationAdultAgedAged, 80 and overCystadenocarcinoma, SerousFemaleGene Expression Regulation, NeoplasticHumansKallikreinsMiddle AgedMultivariate AnalysisNeoplasm GradingOvarian NeoplasmsPrognosisSurvival Analysiskallikrein 4Kallikreins

Identifiers

PMID30811511
PMCPMC6392272
OpenAlexW2915267792

What OpenQuestion holds

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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.