Evidence map›Paper›PMID 26226632›Full record

ArticlePloS one2015

The Cytokinome Profile in Patients with Hepatocellular Carcinoma and Type 2 Diabetes.

Francesca Capone, Eliana Guerriero, Giovanni Colonna, Patrizia Maio, Alessandra Mangia, Raffaele Marfella, Giuseppe Paolisso, Francesco Izzo, Nicoletta Potenza, Luigi Tomeo and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 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 5 institutions in 1 country.

Francesca CaponeCROM, Istituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, Naples, Italy.
Eliana GuerrieroCROM, Istituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, Naples, Italy.
Giovanni ColonnaCenter of Medical Informatics-SIM/AOU-Second University of Naples, Naples, Italy.
Patrizia MaioUnita`Operativa Malattie Infettive, Azienda Ospedaliera di Rilievo Nazionale ''San Giuseppe Moscati", Avellino, Italy.
Alessandra MangiaLiver Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Raffaele MarfellaDepartment of Geriatrics and Metabolic Diseases, Second University of Naples, Naples, Italy.
Giuseppe PaolissoDepartment of Geriatrics and Metabolic Diseases, Second University of Naples, Naples, Italy.
Francesco IzzoIstituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, Naples, Italy.
Nicoletta PotenzaDepartment of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, Caserta, Italy.
Luigi TomeoLaboratorio Borriello SAS, Avellino, Italy.
Giuseppe CastelloCROM, Istituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, Naples, Italy.
Susan CostantiniCROM, Istituto Nazionale Tumori "Fondazione G. Pascale"-IRCCS, Naples, Italy.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Naples Federico II · ITAzienda Ospedaliera S.Giuseppe Moscati · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the dynamics of the complex interaction network of cytokines, defined as ''cytokinome'', can be useful to follow progression and evolution of hepatocellular carcinoma (HCC) from its early stages as well as to define therapeutic strategies. Recently we have evaluated the cytokinome profile in patients with type 2 diabetes (T2D) and/or chronic hepatitis C (CHC) infection and/or cirrhosis suggesting specific markers for the different stages of the diseases. Since T2D has been identified as one of the contributory cause of HCC, in this paper we examined the serum levels of cytokines, growth factors, chemokines, as well as of other cancer and diabetes biomarkers in a discovery cohort of patients with T2D, chronic hepatitis C (CHC) and/or CHC-related HCC comparing them with a healthy control group to define a profile of proteins able to characterize these patients, and to recognize the association between diabetes and HCC. The results have evidenced that the serum levels of some proteins are significantly and differently up-regulated in all the patients but they increased still more when HCC develops on the background of T2D. Our results were verified also using a separate validation cohort. Furthermore, significant correlations between clinical and laboratory data characterizing the various stages of this complex disease, have been found. In overall, our results highlighted that a large and simple omics approach, such as that of the cytokinome analysis, supplemented by common biochemical and clinical data, can give a complete picture able to improve the prognosis of the various stages of the disease progression. We have also demonstrated by means of interactomic analysis that our experimental results correlate positively with the general metabolic picture that is emerging in the literature for this complex multifactorial disease.

Indexed as

AgedCarcinoma, HepatocellularCytokinesDiabetes Mellitus, Type 2FemaleHumansLiver NeoplasmsMaleMiddle AgedCytokines

Identifiers

PMID26226632
PMCPMC4520685
OpenAlexW2234514144

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.