Evidence map›Paper›PMID 34804012›Full record

ArticleFrontiers in immunology2021

Loss of Diacylglycerol Kinase α Enhances Macrophage Responsiveness.

Laryssa C Manigat, Mitchell E Granade, Suchet Taori, Charlotte Anne Miller, Luke R Vass, Xiao-Ping Zhong, Thurl E Harris, Benjamin W Purow

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

8 authors at 2 institutions in 1 country.

Laryssa C ManigatDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA, United States.
Mitchell E GranadeDepartment of Pharmacology, School of Medicine, University of Virginia, Charlottesville, VA, United States.
Suchet TaoriDepartment of Neurology, Division of Neuro-Oncology, University of Virginia, Charlottesville, VA, United States.
Charlotte Anne MillerDepartment of Neurology, Division of Neuro-Oncology, University of Virginia, Charlottesville, VA, United States.
Luke R VassDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA, United States.
Xiao-Ping ZhongDivision of Allergy and Immunology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.
Thurl E HarrisDepartment of Pharmacology, School of Medicine, University of Virginia, Charlottesville, VA, United States.
Benjamin W PurowDepartment of Neurology, Division of Neuro-Oncology, University of Virginia, Charlottesville, VA, United States.
University of Virginia · USDuke Medical Center · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Novel DGKalpha inhibitors and immunotherapy for GBM and melanoma brain metastasisR01CA189524 · NCI · UNIVERSITY OF VIRGINIA · PI PUROW, BENJAMIN W. · 2014 to 2018
$2.5M
Targeting diacylglycerol kinases in glioblastomaR01CA180699 · NCI · UNIVERSITY OF VIRGINIA · PI PUROW, BENJAMIN W. · 2014 to 2017
$1.6M
Regulation of lipin phosphatidic acid phosphatase activityR01GM136900 · NIGMS · UNIVERSITY OF VIRGINIA · PI HARRIS, THURL E. · 2020 to 2023
$1.4M
NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA180699NCI NIH HHS R01 CA189524NIGMS NIH HHS R01 GM136900
6 · The paper itself

Abstract

The diacylglycerol kinases (DGKs) are a family of enzymes responsible for the conversion of diacylglycerol (DAG) to phosphatidic acid (PA). In addition to their primary function in lipid metabolism, DGKs have recently been identified as potential therapeutic targets in multiple cancers, including glioblastoma (GBM) and melanoma. Aside from its tumorigenic properties, DGKα is also a known promoter of T-cell anergy, supporting a role as a recently-recognized T cell checkpoint. In fact, the only significant phenotype previously observed in

Indexed as

AnimalsDiacylglycerol KinaseDisease Models, AnimalMacrophagesMiceMice, Inbred C57BLMice, KnockoutNeoplasmsT-LymphocytesDiacylglycerol KinaseBMDMDGKαdiacylglycerol kinaseimmune regulationmacrophagewound healing

Identifiers

PMID34804012
PMCPMC8603347
OpenAlexW3213993579

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.