Evidence map›Paper›PMID 26420856›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2015

Molecular Pathways: Targeting Diacylglycerol Kinase Alpha in Cancer.

Benjamin Purow

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

43 citing papers in PubMed, 75 citations in OpenAlex.

  1. Enzalutamide-Resistant STEAP4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  13. CaProtein science : a publication of the Protein Society · 2022
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  20. Untargeted metabolomics yields insight into ALS disease mechanisms.Journal of neurology, neurosurgery, and psychiatry · 2020
    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

1 author at 1 institution in 1 country.

Benjamin PurowDepartment of Neurology, University of Virginia, Charlottesville, Virginia. bwp5g@virginia.edu.
University of Virginia · US

Funding

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
NCI NIH HHS R01 CA180699NCI NIH HHS R01CA180699NCI NIH HHS R01 CA189524NCI NIH HHS R01CA189524
6 · The paper itself

Abstract

Lipid kinases have largely been neglected as targets in cancer, and an increasing number of reports suggest diacylglycerol kinase alpha (DGKα) may be one with promising therapeutic potential. DGKα is one of 10 DGK family members that convert diacylglycerol (DAG) to phosphatidic acid (PA), and both DAG and PA are critical lipid second messengers in the plasma membrane. A host of important oncogenic proteins and pathways affect cancer cells in part through DGKα, including the c-Met and VEGF receptors. Others partially mediate the effects of DGKα inhibition in cancer, such as mTOR and HIF-1α. DGKα inhibition can directly impair cancer cell viability, inhibits angiogenesis, and notably may also boost T-cell activation and enhance cancer immunotherapies. Although two structurally similar inhibitors of DGKα were established decades ago, they have seen minimal in vivo usage, and it is unlikely that either of these older DGKα inhibitors will have utility for cancer. An abandoned compound that also inhibits serotonin receptors may have more translational potential as a DGKα inhibitor, but more potent and specific DGKα inhibitors are sorely needed. Other DGK family members may also provide therapeutic targets in cancer, but require further investigation.

Indexed as

ImmunotherapyCell DifferentiationCell SurvivalDiacylglycerol KinaseEnzyme InhibitorsHumansHypoxia-Inducible Factor 1, alpha SubunitLymphocyte ActivationNeoplasmsPhosphatidic AcidsProto-Oncogene Proteins c-metReceptors, Vascular Endothelial Growth FactorSignal TransductionTOR Serine-Threonine KinasesDiacylglycerol KinaseEnzyme InhibitorsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMTOR protein, humanPhosphatidic AcidsProto-Oncogene Proteins c-metReceptors, Vascular Endothelial Growth FactorTOR Serine-Threonine Kinases

Identifiers

PMID26420856
PMCPMC4644682
OpenAlexW2176361029

What OpenQuestion holds

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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.