Evidence map›Paper›PMID 27906674›Full record

ArticleOncotarget2017

Nuclear localization of the CK2α-subunit correlates with poor prognosis in clear cell renal cell carcinoma.

Maj Rabjerg, Barbara Guerra, Aida Oliván-Viguera, Minne Line Nedergaard Mikkelsen, Ralf Köhler, Olaf-Georg Issinger, Niels Marcussen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Protein Kinase CK2 in Cancer Energetics.Frontiers in oncology · 2020
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
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

7 authors at 4 institutions in 2 countries.

Maj RabjergDepartment of Pathology, Odense University Hospital, DK-5000 Odense, Denmark.
Barbara GuerraDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense, Denmark.
Aida Oliván-VigueraAragon Agency for Research and Development (ARAID), IACS, IIS Aragon, 50009 Zaragoza, Spain.
Minne Line Nedergaard MikkelsenDepartment of Pathology, Odense University Hospital, DK-5000 Odense, Denmark.
Ralf KöhlerAragon Agency for Research and Development (ARAID), IACS, IIS Aragon, 50009 Zaragoza, Spain.
Olaf-Georg IssingerDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense, Denmark.
Niels MarcussenDepartment of Pathology, Odense University Hospital, DK-5000 Odense, Denmark.
Odense University Hospital · DKUniversity of Southern Denmark · DKFundacion Agencia Aragonesa para la Investigacion y el Desarrollo · ESInstituto de Investigación Sanitaria Aragón · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein kinase CK2α, one of the two catalytic isoforms of the protein kinase CK2 has been shown to contribute to tumor development, tumor proliferation and suppression of apoptosis in various malignancies. We conducted this study to investigate CK2 expression in different subtypes of Renal Cell Carcinoma (RCC) and in the benign oncocytoma. qRT-PCR, immunohistochemistry and Western blot analyses revealed that CK2α expression was significantly increased at the mRNA and protein levels in clear cell RCC (ccRCC). Also the kinase activity of CK2 was significantly increased in ccRCC compared to normal renal cortex. Nuclear protein expression of CK2α correlated in univariate analysis with poor Progression Free Survival (HR = 8.11, p = 0.016). Functional analyses (cell proliferation assay) revealed an inhibitory effect of Caki-2 cell growth following CK2 inhibition with CX-4945. Our results suggest that CK2α promotes migration and invasion of ccRCC and therefore could serve as a novel prognostic biomarker and molecular therapeutic target in this type of cancer.

Indexed as

Adenoma, OxyphilicAdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Renal CellCasein Kinase IICell Line, TumorCell MovementCell ProliferationFemaleHumansKidney NeoplasmsMaleMiddle AgedNaphthyridinesBiomarkers, TumorCasein Kinase IINaphthyridinesPhenazinesRNA, MessengersilmitasertibCK2 subunitsCK2-targeted therapyCX-4945protein kinase CK2renal cancer

Identifiers

PMID27906674
PMCPMC5352082
OpenAlexW2558631900

What OpenQuestion holds

Textmetadata
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.