Evidence map›Paper›PMID 15785925›Full record

ArticleVirchows Archiv : an international journal of pathology2005

Polo-like kinase isoforms in breast cancer: expression patterns and prognostic implications.

Wilko Weichert, Glen Kristiansen, Klaus-Jürgen Winzer, Mathias Schmidt, Volker Gekeler, Aurelia Noske, Berit-Maria Müller, Silvia Niesporek, Manfred Dietel, Carsten Denkert

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06736717 (A Phase 1b/2 Trial of Onvansertib in Combination With NALIRIFOX for First Line Treatment of Advanced Pancreatic Cancer), which is not on this map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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.

NCT06736717 phase1 / phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Phase 1b/2 Trial of Onvansertib in Combination With NALIRIFOX for First Line Treatment of Advanced Pancreatic Cancer

TypeinterventionalSponsorUniversity of Kansas Medical CenterRan2025 to 2027Enrolled21ConditionsPancreatic CancerArmsOnvansertib, NALIRIFOX
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 144 citations in OpenAlex.

  1. Pooled it
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  18. NAR cancer · 2022
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17 more citing papers are in PubMed but not listed here.

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 2 countries.

Wilko WeichertInstitute of Pathology, Charité University Hospital, Schumannstrasse 20/21, 10117, Berlin, Germany. wilko.weichert@charite.de
Glen Kristiansen
Klaus-Jürgen Winzer
Mathias Schmidt
Volker Gekeler
Aurelia Noske
Berit-Maria Müller
Silvia Niesporek
Manfred Dietel
Carsten Denkert
Charité - Universitätsmedizin Berlin · DEAltana (Germany) · DEAltana (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polo-like kinase (PLK) family members are known to be functionally involved in mitotic signaling and in cytoskeletal reorganization in both normal and malignant cells. In this study, expression of PLK1 and PLK3 was determined immunohistochemically in tissue specimens of 135 breast carcinomas, and expression was correlated with clinicopathological parameters and patient prognosis. Strong PLK isoform overexpression was observed in 42.2% (PLK1) and 47.4% (PLK3) of breast carcinomas when compared with non-transformed breast tissue. A positive correlation of PLK isoform expression with tumor grade, vascular invasion, erbB2/HER-2 expression and markers of proliferative activity was evident. Additionally, an inverse correlation of PLK isoform expression and estrogen receptor status was observed. Overexpression of PLK3 but not of PLK1 was significantly linked to reduced median overall (P<0.001) and relapse-free (P=0.021) survival time. PLK3 expression remained an independent prognostic factor for overall (RR=3.2, P=0.002) and relapse-free (RR=2.9, P=0.049) survival in multivariate survival analysis. These results suggest PLK3 as a novel independent prognostic marker in breast cancer and hint toward a role for PLK isoform overexpression in disease progression. Therefore, in vivo inhibition of PLK family members might represent a rewarding approach in the development of new anticancer drugs for this tumor entity.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularCell Cycle ProteinsFemaleHumansImmunohistochemistryIsoenzymesMiddle AgedPolo-Like Kinase 1Polo-like KinasesPrognosisBiomarkers, TumorCell Cycle ProteinsIsoenzymesPLK3 protein, humanPolo-Like Kinase 1Polo-like KinasesProtein KinasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsTumor Suppressor Proteins

Identifiers

PMID15785925
OpenAlexW2093189315

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.