Evidence map›Paper›PMID 28614356›Full record

ArticlePloS one2017

Anticancer actions of lysosomally targeted inhibitor, LCL521, of acid ceramidase.

Aiping Bai, Cungui Mao, Russell W Jenkins, Zdzislaw M Szulc, Alicja Bielawska, Yusuf A Hannun

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  4. The Role of Ceramide and Sphingolipid Metabolism in Cancer Therapeutics.Journal of oncology research and therapy · 2024
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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

6 authors at 2 institutions in 1 country.

Aiping BaiDepartment of Biochemistry & Molecular Biology, Medical University of South Carolina, Charleston, South Carolina, United States of America.ORCID http://orcid.org/0000-0002-7762-7835
Cungui MaoDepartment of Medicine, Stony Brook University, Stony Brook, New York, United States of America.
Russell W JenkinsDepartment of Biochemistry & Molecular Biology, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Zdzislaw M SzulcDepartment of Biochemistry & Molecular Biology, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Alicja BielawskaDepartment of Biochemistry & Molecular Biology, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Yusuf A HannunDepartment of Medicine, Stony Brook University, Stony Brook, New York, United States of America.
Medical University of South Carolina · USStony Brook University · US

Funding

Sphingolipids in Cancer Therapy and AngiogenesisP01CA097132 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI Daniel Canals · 2003 to 2026
$30.8M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR000062 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$9.4M
RESEARCH PILOT PROJECTS PROGRAMP30GM103339 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI OGRETMEN, BESIM · 2012 to 2016
$5.4M
CERAMIDE ACTIVATED PROTEIN PHOSPHATASESR01CA087584 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI HANNUN, YUSUF AWNI · 2000 to 2015
$4.2M
NCATS NIH HHS UL1 TR000062NCI NIH HHS P01 CA097132NCI NIH HHS R01 CA087584NIGMS NIH HHS P30 GM103339
6 · The paper itself

Abstract

Acid ceramidase, which catalyzes ceramide hydrolysis to sphingosine and free fatty acid mainly in the lysosome, is being recognized as a potential therapeutic target for cancer. B13 is an effective and selective acid ceramidase inhibitor in vitro, but not as effective in cells due to poor access to the lysosomal compartment. In order to achieve targeting of B13 to the lysosome, we designed lysosomotropic N, N-dimethyl glycine (DMG)-conjugated B13 prodrug LCL521 (1,3-di-DMG-B13). Our previous results indicated the efficient delivery of B13 to the lysosome resulted in augmented effects of LCL521 on cellular acid ceramidase as evaluated by effects on substrate/product levels. Our current studies indicate that functionally, this translated into enhanced inhibition of cell proliferation. Moreover, there were greater synergistic effects of LCL521 with either ionizing radiation or Tamoxifen. Taken together, these results clearly indicate that compartmental targeting for the inhibition of acid ceramidase is an efficient and valuable therapeutic strategy.

Indexed as

Acid CeramidaseAntineoplastic AgentsBreast NeoplasmsCell ProliferationCell SurvivalDrug SynergismFemaleHumansNitrobenzenesProdrugsPropanolaminesTamoxifenAcid CeramidaseAntineoplastic AgentsDMG-B13NitrobenzenesProdrugsPropanolaminesTamoxifen

Identifiers

PMID28614356
PMCPMC5470663
OpenAlexW2626284530

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.