Evidence map›Paper›PMID 26933996›Full record

ArticleOncotarget2016

Serum sphingolipidomic analyses reveal an upregulation of C16-ceramide and sphingosine-1-phosphate in hepatocellular carcinoma.

Georgios Grammatikos, Niklas Schoell, Nerea Ferreirós, Dimitra Bon, Eva Herrmann, Harald Farnik, Verena Köberle, Albrecht Piiper, Stefan Zeuzem, Bernd Kronenberger and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 91 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

12 authors at 1 institution in 1 country.

Georgios GrammatikosGoethe University Hospital, Pharmazentrum Frankfurt, Institut für Allgemeine Pharmakologie und Toxikologie, Frankfurt am Main, Germany.
Niklas SchoellGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Nerea FerreirósPharmazentrum Frankfurt, Institut für klinische Pharmakologie, Goethe University Hospital, Frankfurt am Main, Germany.
Dimitra BonGoethe University, Department of Medicine, Institute of Biostatistics and Mathematical Modelling, Frankfurt am Main, Germany.
Eva HerrmannGoethe University, Department of Medicine, Institute of Biostatistics and Mathematical Modelling, Frankfurt am Main, Germany.
Harald FarnikGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Verena KöberleGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Albrecht PiiperGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Stefan ZeuzemGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Bernd KronenbergerGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Oliver WaidmannGoethe University Hospital, Medizinische Klinik 1, Frankfurt am Main, Germany.
Josef PfeilschifterGoethe University Hospital, Pharmazentrum Frankfurt, Institut für Allgemeine Pharmakologie und Toxikologie, Frankfurt am Main, Germany.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have recently shown that major alterations of serum sphingolipid metabolites in chronic liver disease associate significantly with the stage of liver fibrosis in corresponding patients. In the current study we assessed via mass spectrometry serum concentrations of sphingolipid metabolites in a series of 122 patients with hepatocellular carcinoma (HCC) compared to an age- and sex-matched series of 127 patients with cirrhosis. We observed a highly significant upregulation of long and very long chain ceramides (C16-C24) in the serum of patients with HCC as compared to patients with cirrhosis (P < 0.001). Accordingly, dihydro-ceramides, synthetic precursors of ceramides and notably sphingosine, sphingosine-1-phosphate (S1P) and sphinganine-1-phosphate (SA1P) were upregulated in patients with HCC (P < 0.001). Especially the diagnostic accuracy of C16-ceramide and S1P, assessed by receiver operating curve (ROC) analysis, showed a higher area under the curve (AUC) value as compared to alpha fetoprotein (AFP) (0.999 and 0.985 versus 0.823, P < 0.001 respectively). In conclusion, serum levels of sphingolipid metabolites show a significant upregulation in patients with HCC as compared to patients with cirrhosis. Particularly C16-ceramide and S1P may serve as novel diagnostic markers for the identification of HCC in patients with liver diseases. Our data justify further investigations on the role of sphingolipids in HCC.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, HepatocellularCeramidesFemaleHumansLiver CirrhosisLiver NeoplasmsLysophospholipidsMaleMiddle AgedSphingosineUp-RegulationBiomarkers, TumorCeramidesdihydrosphingosine 1-phosphateLysophospholipidsN-palmitoylsphingosineSphingosinesphingosine 1-phosphatebiomarkerdihydroceramideHCCS1Psphingolipid

Identifiers

PMID26933996
PMCPMC4951274
OpenAlexW2300782953

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.