Evidence map›Paper›PMID 24496457›Full record

ArticleBritish journal of cancer2014

Prokineticins and Merkel cell polyomavirus infection in Merkel cell carcinoma.

S Lauttia, H Sihto, H Kavola, V Koljonen, T Böhling, H Joensuu

Abstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

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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

6 authors.

S LauttiaLaboratory of Molecular Oncology, Translational Cancer Biology Program, University of Helsinki, Haartmaninkatu 8, 00290 Helsinki, Finland.
H SihtoLaboratory of Molecular Oncology, Translational Cancer Biology Program, University of Helsinki, Haartmaninkatu 8, 00290 Helsinki, Finland.
H KavolaDepartment of Plastic Surgery, Helsinki University Central Hospital, Topeliuksenkatu 5, 00029 Helsinki, Finland.
V KoljonenDepartment of Plastic Surgery, Helsinki University Central Hospital, Topeliuksenkatu 5, 00029 Helsinki, Finland.
T Böhling1] Department of Pathology, Haartman Institute, University of Helsinki, Haartmaninkatu 3C, 00029 Helsinki, Finland [2] HUSLAB, Helsinki University Central Hospital, Helsinki, Finland.
H Joensuu1] Laboratory of Molecular Oncology, Translational Cancer Biology Program, University of Helsinki, Haartmaninkatu 8, 00290 Helsinki, Finland [2] Department of Oncology, Helsinki University Central Hospital, Haartmaninkatu 4, Helsinki 00029, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProkineticin-1 (PROK1) and prokineticin-2 (PROK2) are chemokine-like proteins that may influence cancer growth by regulating host defence and angiogenesis. Their significance in viral infection-associated cancer is incompletely understood. We studied prokineticins in Merkel cell carcinoma (MCC), a skin cancer linked with Merkel cell polyomavirus (MCPyV) infection.

methodsCarcinoma cell expression of PROK1 and PROK2 and their receptors (PROKR1 and PROKR2) was investigated with immunohistochemistry, and tumour PROK1 and PROK2 mRNA content with quantitative PCR from 98 MCCs. Subsets of tumour infiltrating leukocytes were identified using immunohistochemistry.

resultsMerkel cell polyomavirus-positive MCCs had higher than the median PROK2 mRNA content, whereas MCPyV-negative MCCs contained frequently PROK1 mRNA. Cancers with high tumour PROK2 mRNA content had high counts of tumour infiltrating macrophages (CD68+ and CD163+ cells). Patients with higher than the median PROK2 mRNA content had 44.9% 5-year survival compared with 23.5% among those with a smaller content (hazard ratio (HR): 0.53; 95% confidence interval (CI): 0.34-0.84; P=0.005), whereas the presence of PROK1 mRNA in tumour was associated with unfavourable survival (P=0.052).

conclusionsThe results suggest that prokineticins are associated with MCPyV infection and participate in regulation of the immune response in MCC, and may influence outcome of MCC patients.

Indexed as

AdultCarcinoma, Merkel CellFemaleGastrointestinal HormonesHumansImmunohistochemistryMaleNeuropeptidesPolyomavirus InfectionsReceptors, G-Protein-CoupledReceptors, PeptideSkin NeoplasmsSurvival AnalysisTissue Array AnalysisVascular Endothelial Growth Factor, Endocrine-Gland-DerivedGastrointestinal HormonesNeuropeptidesPROK1 protein, humanPROK2 protein, humanPROKR1 protein, humanPROKR2 protein, humanReceptors, G-Protein-CoupledReceptors, PeptideVascular Endothelial Growth Factor, Endocrine-Gland-Derived

Identifiers

PMID24496457
PMCPMC3960603

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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.