Evidence map›Paper›PMID 31489901›Full record

ArticleInternational journal of molecular sciences2019

Gentamicin Targets Acid Sphingomyelinase in Cancer: The Case of the Human Gastric Cancer NCI-N87 Cells.

Elisabetta Albi, Samuela Cataldi, Maria Rachele Ceccarini, Carmela Conte, Ivana Ferri, Katia Fettucciari, Federica Filomena Patria, Tommaso Beccari, Michela Codini

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  8. Effect of 1α,25(OH)Cancers · 2020
    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

9 authors at 1 institution in 1 country.

Elisabetta AlbiDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. elisabetta.albi@unipg.it.
Samuela CataldiDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. samuelacataldi@libero.it.ORCID 0000-0002-0588-1658
Maria Rachele CeccariniDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. mariarachele.ceccarini@unipg.it.ORCID 0000-0002-5344-4890
Carmela ConteDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. carmela.conte@unipg.it.ORCID 0000-0003-2456-6300
Ivana FerriInstitute of Pathologic Anatomy and Histology, University of Perugia, 06126 Perugia, Italy. ivanaferri@gmail.com.
Katia FettucciariDepartment of Experimental Medicine, University of Perugia, 06100 Perugia, Italy. katia.fettucciari@unipg.it.ORCID 0000-0001-8074-8243
Federica Filomena PatriaDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. patriafederica@gmail.com.ORCID 0000-0001-9010-4150
Tommaso BeccariDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. tommaso.beccari@unipg.it.ORCID 0000-0001-9637-6579
Michela CodiniDepartment of Pharmaceutical Sciences, University of Perugia, 06126 Perugia, Italy. michela.codini@unipg.it.ORCID 0000-0002-1562-4495
University of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging literature implicates acid sphingomyelinase in tumor sensitivity/resistance to anticancer treatments. Gentamicin is a drug commonly used as an antimicrobial but its serendipity effects have been shown. Even though many evidences on the role of gentamicin in cancer have been reported, its mechanism of action is poorly understood. Here, we explored acid sphingomyelinase as a possible new target of gentamicin in cancer. Since gastric cancer is one of the most common cancers and represents the second cause of death in the world, we performed the study in NCI-N87 gastric cancer cell line. The effect of the drug resulted in the inhibition of cell proliferation, including a reduction of cell number and viability, in the decrease of MIB-1 proliferative index as well as in the upregulation of cyclin-dependent kinase inhibitor 1A and 1B (

Indexed as

Antineoplastic AgentsCell Line, TumorDose-Response Relationship, DrugEnzyme InhibitorsGene ExpressionGentamicinsHumansLipid MetabolismSphingomyelin PhosphodiesteraseSphingomyelinsStomach NeoplasmsAntineoplastic AgentsEnzyme InhibitorsGentamicinsSphingomyelin PhosphodiesteraseSphingomyelinscancerdrug targetlipidsphingomyelinsphingomyelinase

Identifiers

PMID31489901
PMCPMC6770866
OpenAlexW2972265031

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.