Evidence map›Paper›PMID 27073147›Full record

ReviewProgress in lipid research2016

Choline kinase alpha-Putting the ChoK-hold on tumor metabolism.

Sean P Arlauckas, Anatoliy V Popov, E James Delikatny

Open access · greenAbstract readReview
In one paragraph

Review in Progress in lipid research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

48 citing papers in PubMed, 73 citations in OpenAlex.

  1. Serum Trimethylamine-International journal of molecular sciences · 2026
    Article
  2. Review
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  10. Review
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  13. The moonlighting function of glycolytic enzyme enolase-1 promotes choline phospholipid metabolism and tumor cell proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Metabolic Reprogramming and Potential Therapeutic Targets in Lymphoma.International journal of molecular sciences · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Bilayer Forming Phospholipids as Targets for Cancer Therapy.International journal of molecular sciences · 2022
    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

3 authors at 1 institution in 1 country.

Sean P ArlauckasDepartment of Radiology, 317 Anatomy-Chemistry Building, 3620 Hamilton Walk, University of Pennsylvania, Philadelphia, PA 19104, USA.
Anatoliy V PopovDepartment of Radiology, 317 Anatomy-Chemistry Building, 3620 Hamilton Walk, University of Pennsylvania, Philadelphia, PA 19104, USA.
E James DelikatnyDepartment of Radiology, 317 Anatomy-Chemistry Building, 3620 Hamilton Walk, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: delikatn@mail.med.upenn.edu.
University of Pennsylvania · US

Funding

PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM008076 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BLENDY, JULIE A · 1985 to 2023
$10.8M
Cerenkov Specific Contrast AgentsR01EB018645 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI DELIKATNY, EDWARD J · 2014 to 2017
$1.4M
NMR and NIR Detection of Phospholipase Activity In VivoR01CA129176 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DELIKATNY, EDWARD J · 2009 to 2012
$1.1M
Near-Infrared Fluorescent Choline Kinase Inhibitors for Cancer Imaging and TherapF31CA180328 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ARLAUCKAS, SEAN · 2013 to 2014
$66k
NCI NIH HHS F31 CA180328NCI NIH HHS R01 CA129176NIBIB NIH HHS R01 EB018645NIGMS NIH HHS T32 GM008076
6 · The paper itself

Abstract

It is well established that lipid metabolism is drastically altered during tumor development and response to therapy. Choline kinase alpha (ChoKα) is a key mediator of these changes, as it represents the first committed step in the Kennedy pathway of phosphatidylcholine biosynthesis and ChoKα expression is upregulated in many human cancers. ChoKα activity is associated with drug resistant, metastatic, and malignant phenotypes, and represents a robust biomarker and therapeutic target in cancer. Effective ChoKα inhibitors have been developed and have recently entered clinical trials. ChoKα's clinical relevance was, until recently, attributed solely to its production of second messenger intermediates of phospholipid synthesis. The recent discovery of a non-catalytic scaffolding function of ChoKα may link growth receptor signaling to lipid biogenesis and requires a reinterpretation of the design and validation of ChoKα inhibitors. Advances in positron emission tomography, magnetic resonance spectroscopy, and optical imaging methods now allow for a comprehensive understanding of ChoKα expression and activity in vivo. We will review the current understanding of ChoKα metabolism, its role in tumor biology and the development and validation of targeted therapies and companion diagnostics for this important regulatory enzyme. This comes at a critical time as ChoKα-targeting programs receive more clinical interest.

Indexed as

AnimalsApoptosisBrain NeoplasmsCholine KinaseDiacylglycerol CholinephosphotransferaseEnzyme InhibitorsHemicholinium 3HumansMagnetic Resonance SpectroscopyPositron-Emission TomographyProtein BindingCholine KinaseDiacylglycerol CholinephosphotransferaseEnzyme InhibitorsHemicholinium 3Choline kinaseInhibitorsLipid metabolismTumor metabolism

Identifiers

PMID27073147
PMCPMC5360181
OpenAlexW2313659012

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.