Evidence map›Paper›PMID 34357010›Full record

ReviewMedicina (Kaunas, Lithuania)2021

Ceramide Metabolism Enzymes-Therapeutic Targets against Cancer.

Ana Gomez-Larrauri, Upasana Das Adhikari, Marta Aramburu-Nuñez, Antía Custodia, Alberto Ouro

Open access · goldAbstract readReview
In one paragraph

Review in Medicina (Kaunas, Lithuania), 2021. 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
1.8field-weighted citation impact, top 14% 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, 35 citations in OpenAlex.

  1. Review
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  4. Article
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  7. Review
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  12. Review
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  15. Research progress on the prevention and treatment of chemotherapy-induced ovarian damage.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
    Review
  16. Article
  17. Article
  18. Ceramide in cerebrovascular diseases.Frontiers in cellular neuroscience · 2023
    Review
  19. Review
  20. 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

5 authors at 3 institutions in 2 countries.

Ana Gomez-LarrauriDepartment of Biochemistry and Molecular Biology, Faculty of Science and Technology, University of the Basque Country, P.O. Box 644, 48980 Bilbao, Spain.
Upasana Das AdhikariRagon Institute of MGH, MITHarvard and HarvardMIT, Cambridge, MA 02139, USA.
Marta Aramburu-NuñezClinical Neurosciences Research Laboratories, Health Research Institute of Santiago de Compostela (IDIS), Travesa da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0002-1212-9851
Antía CustodiaClinical Neurosciences Research Laboratories, Health Research Institute of Santiago de Compostela (IDIS), Travesa da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0003-1122-0351
Alberto OuroClinical Neurosciences Research Laboratories, Health Research Institute of Santiago de Compostela (IDIS), Travesa da Choupana s/n, 15706 Santiago de Compostela, Spain.ORCID 0000-0003-4359-1704
Instituto de Investigación Sanitaria de Santiago · ESHarvard University · USUniversity of the Basque Country · ES

Funding

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia IN606A-2021/015Hezkuntza, Hizkuntza Politika Eta Kultura Saila, Eusko Jaurlaritza POS_2016_1_0092Instituto de Salud Carlos III IFI18/00008
6 · The paper itself

Abstract

Sphingolipids are both structural molecules that are essential for cell architecture and second messengers that are involved in numerous cell functions. Ceramide is the central hub of sphingolipid metabolism. In addition to being the precursor of complex sphingolipids, ceramides induce cell cycle arrest and promote cell death and inflammation. At least some of the enzymes involved in the regulation of sphingolipid metabolism are altered in carcinogenesis, and some are targets for anticancer drugs. A number of scientific reports have shown how alterations in sphingolipid pools can affect cell proliferation, survival and migration. Determination of sphingolipid levels and the regulation of the enzymes that are implicated in their metabolism is a key factor for developing novel therapeutic strategies or improving conventional therapies. The present review highlights the importance of bioactive sphingolipids and their regulatory enzymes as targets for therapeutic interventions with especial emphasis in carcinogenesis and cancer dissemination.

Indexed as

Antineoplastic AgentsNeoplasmsCeramidesHumansInflammationSphingolipidsAntineoplastic AgentsCeramidesSphingolipidsapoptosiscancercell proliferationceramide 1-phosphate (C1P)ceramide (Cer)deoxy-sphingolipidsshingosine 1-phosphate (S1P)sphingolipids (Sphs)

Identifiers

PMID34357010
PMCPMC8303233
OpenAlexW3183268616

What Socratic 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 Socratic graph.