Evidence map›Paper›PMID 34350062›Full record

ArticleOncoimmunology2021

DGKζ exerts greater control than DGKα over CD8

Junchen Gu, Cindy Wang, Carolyn Cao, Jinwen Huang, Sandra Holzhauer, Heshani Desilva, Erin M Wesley, Douglas B Evans, Joseph Benci, Michael Wichroski and 2 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Macrophage DGKActa pharmaceutica Sinica. B · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. 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

12 authors at 5 institutions in 3 countries.

Junchen GuOncology Translational Research, Janssen Research & Development, PA.
Cindy WangOncology Research, Janssen Pharmaceutical, Raritan, NJ.
Carolyn CaoOncology Discovery, Bristol-Myers Squibb, Princeton, New Jersey, USA.
Jinwen HuangOncology Discovery, Bristol-Myers Squibb, Princeton, New Jersey, USA.
Sandra HolzhauerA Division of Versiti, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.
Heshani DesilvaOncology Discovery, Bristol-Myers Squibb, Princeton, New Jersey, USA.
Erin M WesleyA Division of Versiti, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.
Douglas B EvansBlood Research Institute, Blood Center of Wisconsin, a Division of Versiti, Milwaukee.
Joseph BenciOncology Discovery, Bristol Myers Squibb, Princeton, NJ.
Michael WichroskiOncology Discovery, Bristol-Myers Squibb, Princeton, New Jersey, USA.
Susan WeeOncology Discovery, Bristol-Myers Squibb, Princeton, New Jersey, USA.
Matthew J RieseA Division of Versiti, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.
Bristol-Myers Squibb (Germany) · DEBristol-Myers Squibb (United States) · USJanssen (Belgium) · BEMedical College of Wisconsin · USVersiti Blood Center of Wisconsin · US

Funding

Effects of diacylglycerol kinase zeta deficiency on CD8+ T cell functionK08CA151893 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RIESE, MATTHEW J · 2010 to 2014
$861k
NCI NIH HHS K08 CA151893
6 · The paper itself

Abstract

Two isoforms of diacylglycerol kinases (DGKs), DGKα and DGKζ, are primarily responsible for terminating DAG-mediated activation of Ras and PKCθ pathways in T cells. A direct comparison of tumor growth between mice lacking each isoform has not been undertaken. We evaluated the growth of three syngeneic tumor cell lines in mice lacking either DGKα or DGKζ in the presence or absence of treatment with anti-PD1 and determined that (i) mice deficient in DGKζ conferred enhanced control of tumor relative to mice deficient in DGKα and (ii) deficiency of DGKζ acted additively with anti-PD1 in tumor control. Consistent with this finding, functional and RNA-sequencing analyses revealed greater changes in stimulated DGKζ-deficient T cells compared with DGKα-deficient T cells, which were enhanced relative to wildtype T cells. DGKζ also imparted greater regulation than DGKα in human T cells. Together, these data support targeting the ζ isoform of DGKs to therapeutically enhance T cell anti-tumor activity.

Indexed as

Diacylglycerol KinaseT-LymphocytesAnimalsCD8-Positive T-LymphocytesCell Line, TumorMiceDiacylglycerol KinaseDiacylglycerol kinase alphadiacylglycerol kinase zetaT lymphocytetumor immunology

Identifiers

PMID34350062
PMCPMC8296965
OpenAlexW3191401694

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.