Evidence map›Paper›PMID 33081245›Full record

ArticleInternational journal of molecular sciences2020

DAP Kinase-Related Apoptosis-Inducing Protein Kinase 2 (DRAK2) Is a Key Regulator and Molecular Marker in Chronic Lymphocytic Leukemia.

Katarzyna Szoltysek, Carmela Ciardullo, Peixun Zhou, Anna Walaszczyk, Elaine Willmore, Vikki Rand, Scott Marshall, Andy Hall, Christine J Harrison, Jeyanthy Eswaran and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Protein Kinases: Function, Substrates, and Implication in Diseases.International journal of molecular sciences · 2022
    Article
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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

11 authors at 7 institutions in 3 countries.

Katarzyna SzoltysekTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Carmela CiardulloTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Peixun ZhouSchool of Health & Life Sciences, Teesside University, Middlesbrough TS1 3JN, UK.ORCID 0000-0003-2498-5986
Anna WalaszczykInstitute of Biosciences, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Elaine WillmoreTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Vikki RandSchool of Health & Life Sciences, Teesside University, Middlesbrough TS1 3JN, UK.
Scott MarshallDepartment of Haematology, City Hospitals Sunderland NHS Trust, Sunderland SR4 7TP, UK.
Andy HallTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.ORCID 0000-0002-8868-8203
Christine J HarrisonTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Jeyanthy EswaranTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Meera SoundararajanDepartment of Applied Sciences, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne NE1 8ST, UK.ORCID 0000-0003-4687-0151
Newcastle University · GBNorthumbria University · GBTeesside University · GBCentre for Life · GBCity Hospital · GBNewcastle University Medicine Malaysia · MYThe Maria Sklodowska-Curie National Research Institute of Oncology · PL

Funding

JGW Patterson Foundation 116689
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) is the most common adult leukemia in the Western World and it is characterized by a marked degree of clinical heterogeneity. An impaired balance between pro- and anti-apoptotic stimuli determines chemorefractoriness and outcome. The low proliferation rate of CLL cells indicates that one of the primary mechanisms involved in disease development may be an apoptotic failure. Here, we study the clinical and functional significance of DRAK2, a novel stress response kinase that plays a critical role in apoptosis, T-cell biology, and B-cell activation in CLL. We have analyzed CLL patient samples and showed that low expression levels of DRAK2 were significantly associated with unfavorable outcome in our CLL cohort.

Indexed as

AgedApoptosis Regulatory ProteinsBiomarkers, TumorCell ProliferationCell SurvivalDeath-Associated Protein KinasesDown-RegulationFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMAP Kinase Signaling SystemMiddle AgedNF-kappa BProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktApoptosis Regulatory ProteinsBiomarkers, TumorDAPK1 protein, humanDeath-Associated Protein KinasesNF-kappa BProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktReceptor, Transforming Growth Factor-beta Type ISTK17B protein, humanTGFBR1 protein, humanCLLDAPK1DRAK2prognostic indicatorSTK17B

Identifiers

PMID33081245
PMCPMC7593912
OpenAlexW3093180210

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.