Evidence map›Paper›PMID 32024684›Full record

ArticleMolecular cancer therapeutics2020

Selective and Potent CDK8/19 Inhibitors Enhance NK-Cell Activity and Promote Tumor Surveillance.

Marco H Hofmann, Rajeswaran Mani, Harald Engelhardt, Maria A Impagnatiello, Sebastian Carotta, Marc Kerenyi, Seila Lorenzo-Herrero, Jark Böttcher, Dirk Scharn, Heribert Arnhof and 14 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Mediator kinase inhibitors suppress triple-negative breast cancer growth and extend tumor suppression by mTOR and AKT inhibitors.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. 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

24 authors at 3 institutions in 3 countries.

Marco H Hofmann *Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria. marco.hofmann@boehringer-ingelheim.com.ORCID 0000-0001-7557-1156
Rajeswaran Mani *Division of Hematology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.ORCID 0000-0002-2326-7133
Harald Engelhardt *Boehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Maria A ImpagnatielloBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Sebastian CarottaBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Marc KerenyiBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Seila Lorenzo-HerreroDepartment of Functional Biology, Universidad de Oviedo, Instituto de Investigación Biosanitaria del Principado de Asturias (IISPA), IUOPA, Oviedo, Spain.ORCID 0000-0001-9729-3871
Jark BöttcherBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.ORCID 0000-0003-2189-5926
Dirk ScharnBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Heribert ArnhofBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Andreas ZoephelBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.ORCID 0000-0001-5757-1419
Renate SchnitzerBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Thomas GerstbergerBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Michael P SandersonBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Girish RajgolikarDivision of Hematology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Swagata GoswamiDivision of Hematology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Sumithira VasuDivision of Hematology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Peter EttmayerBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.ORCID 0000-0002-8422-2625
Segundo GonzalezDepartment of Functional Biology, Universidad de Oviedo, Instituto de Investigación Biosanitaria del Principado de Asturias (IISPA), IUOPA, Oviedo, Spain.ORCID 0000-0003-4631-9255
Mark PearsonBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Darryl B McConnellBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.ORCID 0000-0002-2537-3458
Norbert KrautBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Natarajan MuthusamyDivision of Hematology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Jürgen MollBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Boehringer Ingelheim (Austria) · ATThe Ohio State University · USUniversidad de Oviedo · ES

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Phosphatase activation as therapeutic strategy for Chronic lymphocyic leukemiaR01CA197844 · NCI · OHIO STATE UNIVERSITY · PI MUTHUSAMY, NATARAJAN, PHELPS, MITCH A · 2015 to 2019
$2.2M
Novel Immunotherapies for Lymphoid MalignanciesR01CA159296 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C., MUTHUSAMY, NATARAJAN · 2012 to 2016
$1.6M
Protein Phosphatase PP2A and DNA damage in cell fate decisions of acute myeloid leukemic cellsF99CA245813 · NCI · OHIO STATE UNIVERSITY · PI GOSWAMI, SWAGATA · 2019 to 2020
$77k
NCI NIH HHS F99 CA245813NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA159296NCI NIH HHS R01 CA197844
6 · The paper itself

Abstract

Natural killer (NK) cells play a pivotal role in controlling cancer. Multiple extracellular receptors and internal signaling nodes tightly regulate NK activation. Cyclin-dependent kinases of the mediator complex (CDK8 and CDK19) were described as a signaling intermediates in NK cells. Here, we report for the first time the development and use of CDK8/19 inhibitors to suppress phosphorylation of STAT1

Indexed as

AnimalsApoptosisBreast NeoplasmsCell ProliferationCyclin-Dependent Kinase 8Cyclin-Dependent KinasesCytotoxicity, ImmunologicFemaleHumansKiller Cells, NaturalLeukemia, Myeloid, AcuteMelanoma, ExperimentalMiceMice, Inbred C57BLMice, Inbred NODMice, SCIDCDK19 protein, humanCDK8 protein, humanCyclin-Dependent Kinase 8Cyclin-Dependent KinasesProtein Kinase InhibitorsSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID32024684
PMCPMC7661742
OpenAlexW3005392824

What OpenQuestion holds

Textmetadata
LicenceTDM
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.