Evidence map›Paper›PMID 34323402›Full record

ArticleClinical and translational medicine2021

The Human Melanoma Proteome Atlas-Complementing the melanoma transcriptome.

Lazaro Hiram Betancourt, Jeovanis Gil, Aniel Sanchez, Viktória Doma, Magdalena Kuras, Jimmy Rodriguez Murillo, Erika Velasquez, Uğur Çakır, Yonghyo Kim, Yutaka Sugihara and 47 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  17. Clinical and translational values of spatial transcriptomics.Signal transduction and targeted therapy · 2022
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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

57 authors at 16 institutions in 11 countries.

Lazaro Hiram BetancourtDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0001-8207-7041
Jeovanis GilDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0003-3601-3893
Aniel SanchezSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.
Viktória Doma2nd Department of Pathology, Semmelweis University, Budapest, Hungary.
Magdalena KurasSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.
Jimmy Rodriguez MurilloDepartment of Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Erika VelasquezSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.ORCID 0000-0002-2169-3315
Uğur ÇakırDepartment of Dermatology, Venerology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Yonghyo KimDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Yutaka SugiharaDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.ORCID 0000-0002-4406-3017
Indira Pla ParadaSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.ORCID 0000-0002-0839-7829
Beáta SzeitzDepartment of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-6414-0537
Roger AppelqvistDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Elisabet WieslanderDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Charlotte WelinderDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Natália Pinto de AlmeidaChemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Nicole WoldmarChemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Matilda Marko-VargaDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Jonatan ErikssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Krzysztof PawłowskiDepartment of Dermatology, Venerology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Bo BaldetorpDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Christian IngvarSUS University hospital Lund, Lund, Sweden.
Håkan OlssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Lotta LundgrenDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Henrik LindbergDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Henriett OskolasDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Boram LeeDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Ethan BergeDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Marie SjögrenDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Carina ErikssonDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Dasol KimChemical Genomics Global Research Lab, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Ho Jeong KwonChemical Genomics Global Research Lab, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0002-6919-833X
Beatrice KnudsenDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Melinda RezeliClinical Protein Science & Imaging, Biomedical Centre, Department of Biomedical Engineering, Lund University, Lund, Sweden.
Johan MalmSection for Clinical Chemistry, Department of Translational Medicine, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.
Runyu HongDepartment of Biochemistry and Molecular Pharmacology, Institute for Systems Genetics, New York University Grossman School of Medicine, New York City, New York.ORCID 0000-0002-0941-351X
Peter HorvathSynthetic and Systems Biology Unit, Biological Research Center, Szeged, Hungary.
A Marcell SzászDepartment of Bioinformatics, Semmelweis University, Budapest, Hungary.
József Tímár2nd Department of Pathology, Semmelweis University, Budapest, Hungary.
Sarolta KárpátiDepartment of Dermatology, Venerology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Peter HorvatovichFaculty of Science and Engineering, Department of Analytical Biochemistry, University of Groningen, Groningen, The Netherlands.
Tasso MiliotisTranslational Science and Experimental Medicine, Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Toshihide NishimuraDepartment of Oncology, St. Marianna University School of Medicine, Kanagawa, Japan.
Harubumi Kato1st Department of Surgery, Tokyo Medical University, Tokyo, Japan.
Erik SteinfelderHQ, ThermoFisher Scientific, San Jose, California.
Madalina OppermannHQ, ThermoFisher Scientific, San Jose, California.
Ken MillerHQ, ThermoFisher Scientific, San Jose, California.
Francesco FlorindiBBMRI-ERIC HQ, Graz, Austria.
Quimin ZhouDepartment of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Gilberto B DomontChemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Luciana PizzattiChemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Fábio C S NogueiraChemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0001-5507-7142
Leticia SzadaiDepartment of Dermatology and Allergology, University of Szeged, Szeged, Hungary.
István Balázs NémethDepartment of Dermatology and Allergology, University of Szeged, Szeged, Hungary.
Henrik EkedahlDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
David FenyöDepartment of Biochemistry and Molecular Pharmacology, Institute for Systems Genetics, New York University Grossman School of Medicine, New York City, New York.
György Marko-VargaClinical Protein Science & Imaging, Biomedical Centre, Department of Biomedical Engineering, Lund University, Lund, Sweden.
Lund University · SESemmelweis University · HUUniversidade Federal do Rio de Janeiro · BRThermo Fisher Scientific (United States) · USNew York University · USTokyo Medical University · JPUniversity of Szeged · HUYonsei University · KRAstraZeneca (Japan) · JPBiobanking and Biomolecular Resources Research Infrastructure Consortium · ATHUN-REN Szegedi Biológiai Kutatóközpont · HUKarolinska Institutet · SEShanghai Jiao Tong University · CNSt. Marianna University School of Medicine · JPUniversity of Groningen · NLUniversity of Utah · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MM500 meta-study aims to establish a knowledge basis of the tumor proteome to serve as a complement to genome and transcriptome studies. Somatic mutations and their effect on the transcriptome have been extensively characterized in melanoma. However, the effects of these genetic changes on the proteomic landscape and the impact on cellular processes in melanoma remain poorly understood. In this study, the quantitative mass-spectrometry-based proteomic analysis is interfaced with pathological tumor characterization, and associated with clinical data. The melanoma proteome landscape, obtained by the analysis of 505 well-annotated melanoma tumor samples, is defined based on almost 16 000 proteins, including mutated proteoforms of driver genes. More than 50 million MS/MS spectra were analyzed, resulting in approximately 13,6 million peptide spectrum matches (PSMs). Altogether 13 176 protein-coding genes, represented by 366 172 peptides, in addition to 52 000 phosphorylation sites, and 4 400 acetylation sites were successfully annotated. This data covers 65% and 74% of the predicted and identified human proteome, respectively. A high degree of correlation (Pearson, up to 0.54) with the melanoma transcriptome of the TCGA repository, with an overlap of 12 751 gene products, was found. Mapping of the expressed proteins with quantitation, spatiotemporal localization, mutations, splice isoforms, and PTM variants was proven not to be predicted by genome sequencing alone. The melanoma tumor molecular map was complemented by analysis of blood protein expression, including data on proteins regulated after immunotherapy. By adding these key proteomic pillars, the MM500 study expands the knowledge on melanoma disease.

Indexed as

TranscriptomeAntineoplastic AgentsBlood ProteinsCell LineChromatography, High Pressure LiquidDatabases, FactualHumansMelanomaMutationProtein Processing, Post-TranslationalProteomeProteomicsProto-Oncogene Proteins B-rafTandem Mass SpectrometryAntineoplastic AgentsBlood ProteinsProteomeProto-Oncogene Proteins B-rafacetylation stoichiometryBRAFdriver mutationshistopathologymetastatic melanomaphosphorylationposttranslational-modificationproteogenomics

Identifiers

PMID34323402
PMCPMC8299047
OpenAlexW3186008659

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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.