Evidence map›Paper›PMID 25874936›Full record

ArticlePloS one2015

A protein deep sequencing evaluation of metastatic melanoma tissues.

Charlotte Welinder, Krzysztof Pawłowski, Yutaka Sugihara, Maria Yakovleva, Göran Jönsson, Christian Ingvar, Lotta Lundgren, Bo Baldetorp, Håkan Olsson, Melinda Rezeli and 8 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Proteomic Findings in Melanoma.Journal of proteomics & bioinformatics · 2016
    Article
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

18 authors at 4 institutions in 5 countries.

Charlotte WelinderOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden; Centre of Excellence in Biological and Medical Mass Spectrometry "CEBMMS", Biomedical Centre D13, Lund University, Lund, Sweden.
Krzysztof PawłowskiWarsaw University of Life Sciences, Warsaw, Poland.
Yutaka SugiharaOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Maria YakovlevaNational Korányi Institute of Pulmonology, Budapest, Hungary; Clinical Protein Science & Imaging, Biomedical Centre, Dept. of Biomedical Engineering, Lund University, Lund, Sweden.
Göran JönssonOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Christian IngvarSurgery, Dept. of Clinical Sciences, Lund University, Skåne University Hospital, Lund, Sweden.
Lotta LundgrenOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden; Skåne University Hospital, Lund, Sweden.
Bo BaldetorpOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Håkan OlssonOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden; Skåne University Hospital, Lund, Sweden; Cancer Epidemiology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Melinda RezeliClinical Protein Science & Imaging, Biomedical Centre, Dept. of Biomedical Engineering, Lund University, Lund, Sweden.
Bo JanssonOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Thomas LaurellCentre of Excellence in Biological and Medical Mass Spectrometry "CEBMMS", Biomedical Centre D13, Lund University, Lund, Sweden; Clinical Protein Science & Imaging, Biomedical Centre, Dept. of Biomedical Engineering, Lund University, Lund, Sweden.
Thomas FehnigerOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden; Centre of Excellence in Biological and Medical Mass Spectrometry "CEBMMS", Biomedical Centre D13, Lund University, Lund, Sweden.
Balazs DömeNational Korányi Institute of Pulmonology, Budapest, Hungary; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Johan MalmSection for Clinical Chemistry, Dept. of Laboratory Medicine, Lund University, Skåne University Hospital in Malmö, Malmö, Sweden.
Elisabet WieslanderOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden.
Toshihide NishimuraOncology and Pathology, Dept. of Clinical Sciences, Lund University, Lund, Sweden; Centre of Excellence in Biological and Medical Mass Spectrometry "CEBMMS", Biomedical Centre D13, Lund University, Lund, Sweden; First Dept. of Surgery, Tokyo Medical University, Tokyo, Japan.
György Marko-VargaCentre of Excellence in Biological and Medical Mass Spectrometry "CEBMMS", Biomedical Centre D13, Lund University, Lund, Sweden; Clinical Protein Science & Imaging, Biomedical Centre, Dept. of Biomedical Engineering, Lund University, Lund, Sweden; First Dept. of Surgery, Tokyo Medical University, Tokyo, Japan.
Lund University · SESkåne University Hospital · SEMedical University of Vienna · ATWarsaw University of Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma has the highest increase of incidence of malignancies in the western world. In early stages, front line therapy is surgical excision of the primary tumor. Metastatic disease has very limited possibilities for cure. Recently, several protein kinase inhibitors and immune modifiers have shown promising clinical results but drug resistance in metastasized melanoma remains a major problem. The need for routine clinical biomarkers to follow disease progression and treatment efficacy is high. The aim of the present study was to build a protein sequence database in metastatic melanoma, searching for novel, relevant biomarkers. Ten lymph node metastases (South-Swedish Malignant Melanoma Biobank) were subjected to global protein expression analysis using two proteomics approaches (with/without orthogonal fractionation). Fractionation produced higher numbers of protein identifications (4284). Combining both methods, 5326 unique proteins were identified (2641 proteins overlapping). Deep mining proteomics may contribute to the discovery of novel biomarkers for metastatic melanoma, for example dividing the samples into two metastatic melanoma "genomic subtypes", ("pigmentation" and "high immune") revealed several proteins showing differential levels of expression. In conclusion, the present study provides an initial version of a metastatic melanoma protein sequence database producing a total of more than 5000 unique protein identifications. The raw data have been deposited to the ProteomeXchange with identifiers PXD001724 and PXD001725.

Indexed as

Databases, ProteinBiological Specimen BanksChromatography, LiquidComputational BiologyCutaneous Malignant MelanomaData MiningDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMelanomaNeoplasm MetastasisProteomicsSequence Analysis, ProteinSkin NeoplasmsSweden

Identifiers

PMID25874936
PMCPMC4395420
OpenAlexW2046887897

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.