Evidence map›Paper›PMID 31409741›Full record

ArticleJournal of lipid research2019

High FA2H and UGT8 transcript levels predict hydroxylated hexosylceramide accumulation in lung adenocarcinoma.

Anne-Marie Lemay, Olivier Courtemanche, Timothy A Couttas, Giuleta Jamsari, Andréanne Gagné, Yohan Bossé, Philippe Joubert, Anthony S Don, David Marsolais

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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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 3 institutions in 2 countries.

Anne-Marie LemayInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada.
Olivier CourtemancheInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada.
Timothy A CouttasCentenary Institute, University of Sydney, Camperdown, NSW 2006, Australia.
Giuleta JamsariPrince of Wales Clinical School, University of New South Wales, Sydney, NSW 2052, Australia.
Andréanne GagnéInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada.
Yohan BosséInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada.ORCID 0000-0002-3067-3711
Philippe JoubertInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada.ORCID 0000-0001-7784-6387
Anthony S DonCentenary Institute, University of Sydney, Camperdown, NSW 2006, Australia.ORCID 0000-0003-1655-1184
David MarsolaisInstitut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, QC G1V 4G5, Canada David.Marsolais@criucpq.ulaval.ca.ORCID 0000-0002-8935-6657
Institut universitaire de cardiologie et de pneumologie de Québec · CAThe University of Sydney · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer causes more deaths than any other cancer. Sphingolipids encompass metabolically interconnected species whose balance has pivotal effects on proliferation, migration, and apoptosis. In this study, we paralleled quantification of sphingolipid species with quantitative (q)PCR analyses of metabolic enzymes in order to identify dysregulated routes of sphingolipid metabolism in different subtypes of lung cancers. Lung samples were submitted to histopathological reexamination in order to confirm cancer type/subtype, which included adenocarcinoma histological subtypes and squamous cell and neuroendocrine carcinomas. Compared with benign lesions and tumor-free parenchyma, all cancers featured decreased sphingosine-1-phosphate and SMs. qPCR analyses evidenced differential mechanisms leading to these alterations between cancer types, with neuroendocrine carcinomas upregulating

Indexed as

Adenocarcinoma of LungAdultAged, 80 and overCeramidesFemaleGanglioside GalactosyltransferaseHumansHydroxylationMaleMiddle AgedMixed Function OxygenasesRNA, MessengerCeramidesfatty acid alpha-hydroxylaseGanglioside GalactosyltransferaseMixed Function OxygenasesRNA, MessengerUGT8 protein, human2-hydroxyhexosylceramidecancerfatty acid 2-hydroxylasefatty acidsgene expressionmass spectrometryneuroendocrinesphingolipidsquamousuridine 5′-diphosphate-glycosyltransferase 8

Identifiers

PMID31409741
PMCPMC6795083
OpenAlexW2967407933

What OpenQuestion holds

Textmetadata
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.