Evidence map›Paper›PMID 28434262›Full record

ReviewExpert opinion on therapeutic targets2017

The emergence of acid ceramidase as a therapeutic target for acute myeloid leukemia.

Su-Fern Tan, Jennifer M Pearson, David J Feith, Thomas P Loughran

Abstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  15. Ceramide Analogue SACLAC Modulates Sphingolipid Levels andMolecular cancer research : MCR · 2020
    Article
  16. Review
  17. Article
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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 2 institutions in 1 country.

Su-Fern Tana Department of Medicine , University of Virginia , Charlottesville , VA , USA.
Jennifer M Pearsona Department of Medicine , University of Virginia , Charlottesville , VA , USA.
David J Feitha Department of Medicine , University of Virginia , Charlottesville , VA , USA.
Thomas P Loughrana Department of Medicine , University of Virginia , Charlottesville , VA , USA.
University of Virginia · USUniversity of Virginia Cancer Center

Funding

Tissue Repository and Animal Models CoreP01CA171983 · NCI · UNIVERSITY OF VIRGINIA · PI FISHER-WELLMAN, KELSEY H · 2013 to 2024
$19.9M
TRAINING IN THE PHARMACOLOGICAL SCIENCEST32GM007055 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LYNCH, KEVIN R. · 1985 to 2022
$7.2M
NCI NIH HHS P01 CA171983NIGMS NIH HHS T32 GM007055
6 · The paper itself

Abstract

introductionAcute myeloid leukemia (AML) is the most common adult leukemia. Only a fraction of AML patients will survive with existing chemotherapy regimens. Hence, there is an urgent and unmet need to identify novel targets and develop better therapeutics in AML. In the past decade, the field of sphingolipid metabolism has emerged into the forefront of cancer biology due to its importance in cancer cell proliferation and survival. In particular, acid ceramidase (AC) has emerged as a promising therapeutic target due to its role in neutralizing the pro-death effects of ceramide. Areas covered: This review highlights key information about AML biology as well as current knowledge on dysregulated sphingolipid metabolism in cancer and AML. We describe AC function and dysregulation in cancer, followed by a review of studies that report elevated AC in AML and compounds known to inhibit the enzyme. Expert opinion: AML has a great need for new drug targets and better therapeutic agents. The finding of elevated AC in AML supports the concept that this enzyme represents a novel and realistic therapeutic target for this common leukemia. More effort is needed towards developing better AC inhibitors for clinical use and combination treatment with existing AML therapies.

Indexed as

Acid CeramidaseAdultAnimalsAntineoplastic AgentsCell ProliferationCell SurvivalDrug DesignEnzyme InhibitorsHumansLeukemia, Myeloid, AcuteMolecular Targeted TherapySurvival RateAcid CeramidaseAntineoplastic AgentsEnzyme InhibitorsAcid ceramidaseacute myeloid leukemiaceramidesphingosine 1-phosphate

Identifiers

PMID28434262
PMCPMC5738025
OpenAlexW2608864912

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.