Evidence map›Paper›PMID 29072691›Full record

ArticleCell death & disease2017

Phosphoprotein enriched in diabetes (PED/PEA15) promotes migration in hepatocellular carcinoma and confers resistance to sorafenib.

Cristina Quintavalle, Sravanth Kumar Hindupur, Luca Quagliata, Pierlorenzo Pallante, Cecilia Nigro, Gerolama Condorelli, Jesper Bøje Andersen, Katrin Elisabeth Tagscherer, Wilfried Roth, Francesco Beguinot and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. 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
2.8field-weighted citation impact, top 8% 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, 43 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

14 authors at 5 institutions in 4 countries.

Cristina QuintavalleInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.ORCID 0000-0002-7432-9170
Sravanth Kumar HindupurBiozentrum, University of Basel, Basel, Switzerland.
Luca QuagliataInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.
Pierlorenzo PallanteInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.
Cecilia NigroURT of the Institute of Experimental Endocrinology and Oncology 'G. Salvatore', National Council of Research, Naples, Italy.
Gerolama CondorelliIstituto per l'Endocrinologia e l'Oncologia Sperimentale (IEOS), 'G. Salvatore', Consiglio Nazionale delle Ricerche (CNR), Naples, Italy.
Jesper Bøje AndersenBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Katrin Elisabeth TagschererInstitute of Pathology, University Medical Center Mainz, Mainz, Germany.
Wilfried RothInstitute of Pathology, University Medical Center Mainz, Mainz, Germany.
Francesco BeguinotURT of the Institute of Experimental Endocrinology and Oncology 'G. Salvatore', National Council of Research, Naples, Italy.
Markus Hermann HeimDivision of Gastroenterology, University Hospital of Basel, Basel, Switzerland.
Charlotte Kiu Yan NgInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.
Salvatore PiscuoglioInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.ORCID 0000-0003-2686-2939
Matthias Sebastian MatterInstitute of Pathology, University Hospital of Basel, Basel, Switzerland.
University Hospital of Basel · CHInstitute for Experimental Endocrinology and Oncology · ITJohannes Gutenberg University Mainz · DEUniversity of Basel · CHUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the third-leading cause of cancer-related death with limited treatment options and frequent resistance to sorafenib, the only drug currently approved for first-line therapy. Therefore, better understanding of HCC tumor biology and its resistance to treatment is urgently needed. Here, we analyzed the role of phosphoprotein enriched in diabetes (PED) in HCC. PED has been shown to regulate cell proliferation, apoptosis and migration in several types of cancer. However, its function in HCC has not been addressed yet. Our study revealed that both transcript and protein levels of PED were significantly high in HCC compared with non-tumoral tissue. Clinico-pathological correlation revealed that PED

Indexed as

AdolescentAdultAgedAged, 80 and overApoptosis Regulatory ProteinsCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationChildDrug Resistance, NeoplasmHumansIntracellular Signaling Peptides and ProteinsLiver NeoplasmsMiddle AgedNiacinamideApoptosis Regulatory ProteinsIntracellular Signaling Peptides and ProteinsNiacinamidePEA15 protein, humanPhenylurea CompoundsPhosphoproteinsSorafenib

Identifiers

PMID29072691
PMCPMC5682677
OpenAlexW2766752058

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.