Evidence map›Paper›PMID 37279374›Full record

ArticleBioconjugate chemistry2023

All-in-One Pyruvate Dehydrogenase Kinase Inhibitor for Tracking, Targeting, and Enhanced Efficacy.

Xiao Zhang, Shrita Sarkar, Akash Ashokan, Bapurao Surnar, Nagesh Kolishetti, Shanta Dhar

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Xiao ZhangSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, University of Miami, Miami, Florida 33136, United States.
Shrita SarkarSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, University of Miami, Miami, Florida 33136, United States.
Akash AshokanSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, University of Miami, Miami, Florida 33136, United States.
Bapurao SurnarSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, University of Miami, Miami, Florida 33136, United States.
Nagesh KolishettiDepartment of Immunology and Nano-Medicine, Herbert Wertheim, College of Medicine, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0001-5574-673X
Shanta DharSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, University of Miami, Miami, Florida 33136, United States.ORCID 0000-0003-3042-5272

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Daniel Bilbao · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

The metabolic preference of cells toward glycolysis often indicates a diseased state ranging from cancer to other dysfunctions. When a particular cell type utilizes glycolysis as a major energy production pathway, their mitochondria become impaired resulting a cascade of events which eventually contributes to resistance toward therapies to tackle such diseases. In abnormal tissues such as seen in the tumor microenvironment, when cancer cells utilize glycolysis, other cell types such as the immune cells switch their metabolism and prefer such glycolysis. As a result, utilization of therapies to destroy glycolytic preferences by cancer cells results in destruction of immune cells contributing toward an immunosuppressive phenotype. Thus, development of targeted, trackable, comparatively stable glycolysis inhibitors is urgently needed to manage diseases where glycolysis is preferred for disease progression. No glycolysis inhibitor exists which can be tracked and packaged in a delivery vehicle for efficient targeted deployment. Here, we report synthesis, characterization, and formulation of an all-in-one glycolysis inhibitor and document the therapeutic potential along with trackability and glycolysis inhibition of this inhibitor by utilizing an

Indexed as

NeoplasmsGlycolysisHumansPyruvate Dehydrogenase Acetyl-Transferring KinaseTumor MicroenvironmentPyruvate Dehydrogenase Acetyl-Transferring Kinase

Identifiers

PMID37279374
PMCPMC10903362

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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.