Evidence map›Paper›PMID 26384346›Full record

ArticleOncotarget2015

MCT4 surpasses the prognostic relevance of the ancillary protein CD147 in clear cell renal cell carcinoma.

Pascale Fisel, Viktoria Stühler, Jens Bedke, Stefan Winter, Steffen Rausch, Jörg Hennenlotter, Anne T Nies, Arnulf Stenzl, Marcus Scharpf, Falko Fend and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-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

16 citing papers in PubMed, 28 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

13 authors at 3 institutions in 1 country.

Pascale FiselDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Viktoria StühlerDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Jens BedkeDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Stefan WinterDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Steffen RauschDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Jörg HennenlotterDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Anne T NiesDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Arnulf StenzlDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Marcus ScharpfInstitute of Pathology and Neuropathology, University Hospital Tuebingen, Tuebingen, Germany.
Falko FendInstitute of Pathology and Neuropathology, University Hospital Tuebingen, Tuebingen, Germany.
Stephan KruckDepartment of Urology, University Hospital Tuebingen, Tuebingen, Germany.
Matthias SchwabDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Elke SchaeffelerDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
University of Tübingen · DEDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledCluster of differentiation 147 (CD147/BSG) is a transmembrane glycoprotein mediating oncogenic processes partly through its role as binding partner for monocarboxylate transporter MCT4/SLC16A3. As demonstrated for MCT4, CD147 is proposed to be associated with progression in clear cell renal cell carcinoma (ccRCC). In this study, we evaluated the prognostic relevance of CD147 in comparison to MCT4/SLC16A3 expression and DNA methylation.

methodsCD147 protein expression was assessed in two independent ccRCC-cohorts (n = 186, n = 59) by immunohistochemical staining of tissue microarrays and subsequent manual as well as automated software-supported scoring (Tissue Studio, Definien sAG). Epigenetic regulation of CD147 was investigated using RNAseq and DNA methylation data of The Cancer Genome Atlas. These results were validated in our cohort. Relevance of prognostic models for cancer-specific survival, comprising CD147 and MCT4 expression or SLC16A3 DNA methylation, was compared using chi-square statistics.

resultsCD147 protein expression generated with Tissue Studio correlated significantly with those from manual scoring (P < 0.0001, rS = 0.85), indicating feasibility of software-based evaluation exemplarily for the membrane protein CD147 in ccRCC. Association of CD147 expression with patient outcome differed between cohorts. DNA methylation in the CD147/BSG promoter was not associated with expression. Comparison of prognostic relevance of CD147/BSG and MCT4/SLC16A3, showed higher significance for MCT4 expression and superior prognostic power for DNA methylation at specific CpG-sites in the SLC16A3 promoter (e.g. CD147 protein: P = 0.7780,Harrell's c-index = 53.7% vs. DNA methylation: P = 0.0076, Harrell's c-index = 80.0%).

conclusionsPrognostic significance of CD147 protein expression could not surpass that of MCT4, especially of SLC16A3 DNA methylation, corroborating the role of MCT4 as prognostic biomarker for ccRCC.

Indexed as

AdolescentAdultAgedAged, 80 and overBasiginBiomarkers, TumorCarcinoma, Renal CellCell Line, TumorDisease ProgressionDNA MethylationFemaleHumansMaleMiddle AgedMonocarboxylic Acid TransportersMuscle ProteinsBasiginBiomarkers, TumorBSG protein, humanMonocarboxylic Acid TransportersMuscle ProteinsRNA, MessengerSLC16A4 protein, humanccRCCCD147DNA methylationMCT4Pathology Sectionprognosis

Identifiers

PMID26384346
PMCPMC4741556
OpenAlexW2106882655

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Registered trials

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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.