Evidence map›Paper›PMID 40322912›Full record

ArticleJournal of proteome research2025

Melanoma Proteomics Unveiled: Harmonizing Diverse Data Sets for Biomarker Discovery and Clinical Insights via MEL-PLOT.

Áron Bartha, Boglárka Weltz, Lazaro Hiram Betancourt, Jeovanis Gil, Natália Pinto de Almeida, Giampaolo Bianchini, Beáta Szeitz, Leticia Szadai, Indira Pla, Lajos V Kemény and 27 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

37 authors.

Áron BarthaDepartment of Bioinformatics, Semmelweis University, Budapest 1085, Hungary.
Boglárka WeltzDepartment of Bioinformatics, Semmelweis University, Budapest 1085, Hungary.
Lazaro Hiram BetancourtEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Jeovanis GilEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Natália Pinto de AlmeidaEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Giampaolo BianchiniSan Raffaele Hospital, Milan, 20132, Italy.
Beáta SzeitzDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, Budapest, 1085, Hungary.
Leticia SzadaiDepartment of Dermatology and Allergology, University of Szeged, Szeged, 6720, Hungary.
Indira PlaEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Lajos V KeményHCEMM-SU Translational Dermatology Research Group, Semmelweis University, Budapest, 1085, Hungary.
Ágnes Judit JánosiDepartment of Dermatology and Allergology, University of Szeged, Szeged, 6720, Hungary.
Runyu HongInstitute for Systems Genetics, NYU Grossman School of Medicine, New York, New York 10016, United States.
Ahmad RajehDepartment of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
Fábio NogueiraProteomics Unit, Institute of Chemistry and Research Center for Precision Medicine, Institute of Biophysics Carlos Chagas Filho, Federal Univesity of Rio de Janeiro, Rio de Janeiro, 21941-170, Brazil.ORCID 0000-0001-5507-7142
Viktória DomaDepartment of Dermatology, Venerology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, 1085, Hungary.
Nicole WoldmarEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Jéssica GuedesEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Zsuzsanna ÚjfaludiUniversity of Szeged, Albert Szent-Györgyi Clinical Centre, Department of Pathology, 6720, Szeged, Hungary.
Yonghyo KimDrug Discovery Platform Research Center, Therapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
Tibor SzarvasDepartment of Urology, Semmelweis University, Budapest, 1082, Hungary.
Zoltan PahiDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, Szeged H-6725, Hungary.
Tibor PankotaiDepartment of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, Szeged H-6725, Hungary.
A Marcell SzaszDivision of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1085 Budapest, Hungary.
Aniel SanchezSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö,205 02, Sweden.
Bo BaldetorpDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund,221 84, Sweden.
József TímárDepartment of Pathology, Forensic and Insurance Medicine, Faculty of Medicine, Semmelweis University, Budapest,1085, Hungary.
István Balázs NémethDepartment of Dermatology and Allergology, University of Szeged, Szeged, 6720, Hungary.
Sarolta KárpátiDepartment of Dermatology, Venerology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, 1085, Hungary.
Roger AppelqvistClinical Protein Science & Imaging, Biomedical Centre, Department of Biomedical Engineering, Lund University, Lund, 223 63, Sweden.
Gilberto Barbosa DomontProteomics Unit, Institute of Chemistry and Research Center for Precision Medicine, Institute of Biophysics Carlos Chagas Filho, Federal Univesity of Rio de Janeiro, Rio de Janeiro, 21941-170, Brazil.ORCID 0000-0002-1329-6483
Krzysztof PawlowskiSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö,205 02, Sweden.
Elisabet WieslanderSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö,205 02, Sweden.
Johan MalmSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Lund 21428, Sweden.
David FenyoInstitute for Systems Genetics, NYU Grossman School of Medicine, New York, New York 10016, United States.ORCID 0000-0001-5049-3825
Peter HorvatovichUniversity of Groningen, Groningen Research Institute of Pharmacy, Analytical Biochemistry, Groningen, 9711, The Netherlands.ORCID 0000-0003-2218-1140
György Marko-VargaEuropean Cancer Moonshot Lund Center, Lund, SE-221 84, Sweden.
Balázs GyőrffyDepartment of Bioinformatics, Semmelweis University, Budapest 1085, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using several melanoma proteomics data sets we created a single analysis platform that enables the discovery, knowledge build, and validation of diagnostic, predictive, and prognostic biomarkers at the protein level. Quantitative mass-spectrometry-based proteomic data was obtained from five independent cohorts, including 489 tissue samples from 394 patients with accompanying clinical metadata. We established an interactive R-based web platform that enables the comparison of protein levels across diverse cohorts, and supports correlation analysis between proteins and clinical metadata including survival outcomes. By comparing differential protein levels between metastatic, primary tumor, and nonmalignant samples in two of the cohorts, we identified 274 proteins showing significant differences among the sample types. Further analysis of these 274 proteins in lymph node metastatic samples from a third cohort revealed that 45 proteins exhibited a significant effect on patient survival. The three most significant proteins were HP (HR = 4.67, p = 2.8e-06), LGALS7 (HR = 3.83, p = 2.9e-05), and UBQLN1 (HR = 3.2, p = 4.8e-05). The user-friendly interactive web platform, accessible at https://www.tnmplot.com/melanoma, provides an interactive interface for the analysis of proteomic and clinical data. The MEL-PLOT platform, through its interactive capabilities, streamlines the creation of a comprehensive knowledge base, empowering hypothesis formulation and diligent monitoring of the most recent advancements in the domains of biomedical research and drug development.

Indexed as

Biomarkers, TumorMelanomaProteomicsHumansLymphatic MetastasisMalePrognosisSoftwareBiomarkers, Tumormass spectrometryproteomicsskin cancersurvivaltumor progression

Identifiers

PMID40322912
PMCPMC12150306

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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.