Evidence map›Paper›PMID 25750912›Full record

ArticleFrontiers in cell and developmental biology2015

CK1δ in lymphoma: gene expression and mutation analyses and validation of CK1δ kinase activity for therapeutic application.

B Sophia Winkler, Franziska Oltmer, Julia Richter, Joachim Bischof, Pengfei Xu, Timo Burster, Frank Leithäuser, Uwe Knippschild

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 1 institution in 1 country.

B Sophia WinklerDepartment of Pathology, Ulm University Hospital Ulm, Germany.
Franziska OltmerDepartment of General and Visceral Surgery, Surgery Center, Ulm University Hospital Ulm, Germany.
Julia RichterDepartment of General and Visceral Surgery, Surgery Center, Ulm University Hospital Ulm, Germany.
Joachim BischofDepartment of General and Visceral Surgery, Surgery Center, Ulm University Hospital Ulm, Germany.
Pengfei XuDepartment of General and Visceral Surgery, Surgery Center, Ulm University Hospital Ulm, Germany.
Timo BursterDepartment of Neurosurgery, Ulm University Hospital Ulm, Germany.
Frank LeithäuserDepartment of Pathology, Ulm University Hospital Ulm, Germany.
Uwe KnippschildDepartment of General and Visceral Surgery, Surgery Center, Ulm University Hospital Ulm, Germany.
University Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of lymphoid neoplasms has improved considerably during the last decades. However, treatment response for some lymphoid neoplasms is still poor, indicating the need for new therapeutic approaches. One promising new strategy is the inhibition of kinases regulating key signal transduction pathways, which are of central importance in tumorigenesis. Kinases of the CK1 family may represent an attractive drug target since CK1 expression and/or activity are associated with the pathogenesis of malignant diseases. Over the last years efforts were taken to develop highly potent and selective CK1-specific inhibitor compounds and their therapeutic potential has now to be proved in pre-clinical trials. Therefore, we analyzed expression and mutational status of CK1δ in several cell lines representing established lymphoma entities, and also measured the mRNA expression level in primary lymphoma tissue as well as in non-neoplastic blood cells. For a selection of lymphoma cell lines we furthermore determined CK1δ kinase activity and demonstrated therapeutic potential of CK1-specific inhibitors as a putative therapeutic option in the treatment of lymphoid neoplasms.

Indexed as

cell cycleCK1inhibitorlymphomamutation analysistherapy

Identifiers

PMID25750912
PMCPMC4335261
OpenAlexW2091745197

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.