Evidence map›Paper›PMID 31500224›Full record

ReviewInternational journal of molecular sciences2019

Protein Kinase CK2-A Putative Target for the Therapy of Diabetes Mellitus?

Emmanuel Ampofo, Lisa Nalbach, Michael D Menger, Mathias Montenarh, Claudia Götz

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. Review
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  14. Review
  15. Article
  16. Role of Protein Kinase CK2 in Aberrant Lipid Metabolism in Cancer.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  17. Protein Kinase CK2 Controls CaInternational journal of molecular sciences · 2020
    Article
  18. Protein Kinase CK2 in Cancer Energetics.Frontiers in oncology · 2020
    Review
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

5 authors at 1 institution in 1 country.

Emmanuel AmpofoInstitute for Clinical & Experimental Surgery, Saarland University, 66424 Homburg, Germany. emmanuel.ampofo@uks.eu.
Lisa NalbachInstitute for Clinical & Experimental Surgery, Saarland University, 66424 Homburg, Germany. lisa.nalbach@uks.eu.
Michael D MengerInstitute for Clinical & Experimental Surgery, Saarland University, 66424 Homburg, Germany. michael.menger@uks.eu.
Mathias MontenarhMedical Biochemistry and Molecular Biology, Saarland University, 66424 Homburg, Germany. mathias.montenarh@uks.eu.
Claudia GötzMedical Biochemistry and Molecular Biology, Saarland University, 66424 Homburg, Germany. claudia.goetz@uks.eu.ORCID 0000-0001-7115-0485
Saarland University · DE

Funding

Schwiete Stiftung project Nr. 06/2015
6 · The paper itself

Abstract

Since diabetes is a global epidemic, the development of novel therapeutic strategies for the treatment of this disease is of major clinical interest. Diabetes is differentiated in two types: type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM). T1DM arises from an autoimmune destruction of insulin-producing β-cells whereas T2DM is characterized by an insulin resistance, an impaired insulin reaction of the target cells, and/or dysregulated insulin secretion. In the past, a growing number of studies have reported on the important role of the protein kinase CK2 in the regulation of the survival and endocrine function of pancreatic β-cells. In fact, inhibition of CK2 is capable of reducing cytokine-induced loss of β-cells and increases insulin expression as well as secretion by various pathways that are regulated by reversible phosphorylation of proteins. Moreover, CK2 inhibition modulates pathways that are involved in the development of diabetes and prevents signal transduction, leading to late complications such as diabetic retinopathy. Hence, targeting CK2 may represent a novel therapeutic strategy for the treatment of diabetes.

Indexed as

Casein Kinase IIClinical Trials as TopicDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Gene Expression RegulationHumansHypoglycemic AgentsInsulin ResistanceInsulin-Secreting CellsMolecular Targeted TherapySignal TransductionCasein Kinase IICSNK2A1 protein, humanHypoglycemic AgentsCK2diabetesinsulinβ-cells

Identifiers

PMID31500224
PMCPMC6770776
OpenAlexW2971942600

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.