Evidence map›Paper›PMID 30989436›Full record

ArticleMolecular imaging and biology2020

Evaluation of Glycolytic Response to Multiple Classes of Anti-glioblastoma Drugs by Noninvasive Measurement of Pyruvate Kinase M2 Using [

Corinne Beinat, Chirag B Patel, Yuanyang Xie, Sanjiv S Gambhir

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Molecular imaging and biology, 2020. 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
1.6field-weighted citation impact, top 16% 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, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. A Clinical PET Imaging Tracer ([Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  6. Review
  7. Review
  8. Article
  9. Human biodistribution and radiation dosimetry of [European journal of nuclear medicine and molecular imaging · 2020
    Article
  10. 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

4 authors at 3 institutions in 2 countries.

Corinne BeinatMolecular Imaging Program at Stanford, Department of Radiology, James H. Clark Center, Stanford University School of Medicine, 318 Campus Drive, E153, Stanford, CA, 94305, USA.
Chirag B PatelMolecular Imaging Program at Stanford, Department of Radiology, James H. Clark Center, Stanford University School of Medicine, 318 Campus Drive, E153, Stanford, CA, 94305, USA.
Yuanyang XieMolecular Imaging Program at Stanford, Department of Radiology, James H. Clark Center, Stanford University School of Medicine, 318 Campus Drive, E153, Stanford, CA, 94305, USA.
Sanjiv S GambhirMolecular Imaging Program at Stanford, Department of Radiology, James H. Clark Center, Stanford University School of Medicine, 318 Campus Drive, E153, Stanford, CA, 94305, USA. sgambhir@stanford.edu.ORCID 0000-0002-2711-7554
Stanford University · USCentral South University · CNStanford Medicine · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
NCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

purposePyruvate kinase M2 (PKM2) catalyzes the final step in glycolysis, the key process of tumor metabolism. PKM2 is found in high levels in glioblastoma (GBM) cells with marginal expression within healthy brain tissue, rendering it a key biomarker of GBM metabolic re-programming. Our group has reported the development of a novel radiotracer, 1-((2-fluoro- 6-[ PROCEDURE: U87 human GBM cells were treated with the IC50 concentration of various agents used in the treatment of GBM, including alkylating agents (temozolomide, carmustine, lomustine, procarbazine), inhibitor of topoisomerase I (irinotecan), vascular endothelial and epidermal growth factor receptor inhibitors (cediranib and erlotinib, respectively) anti-metabolite (5-fluorouracil), microtubule inhibitor (vincristine), and metabolic agents (dichloroacetate and IDH1 inhibitor ivosidenib). Following drug exposure for three or 6 days (n = 6 replicates per condition), the radiotracer uptake of [

resultsSignificant interactions were found between the treatment agent (n = 12 conditions total comprised 11 drugs and vehicle) and the duration of treatment (3- or 6-day exposure to each drug) on the cellular uptake of [

conclusionsThese proof of principle studies emphasize the superiority of [

Indexed as

GlycolysisAntineoplastic AgentsBrain NeoplasmsEvaluation Studies as TopicFluorodeoxyglucose F18GlioblastomaHumansPositron-Emission TomographyPyruvate KinaseRadiopharmaceuticalsTumor Cells, CulturedAntineoplastic AgentsFluorodeoxyglucose F18Pyruvate KinaseRadiopharmaceuticals[18F]DASA-23[18F]FDGGlioblastomaGlycolysisPyruvate kinase M2

Identifiers

PMID30989436
PMCPMC7959514
OpenAlexW2939631904

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.