Evidence map›Paper›PMID 27600516›Full record

ArticleCancer immunology, immunotherapy : CII2016

Mass spectrometric analysis of the HLA class I peptidome of melanoma cell lines as a promising tool for the identification of putative tumor-associated HLA epitopes.

Andreas Gloger, Danilo Ritz, Tim Fugmann, Dario Neri

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Iranian journal of biotechnology · 2024
    Article
  5. Article
  6. Article
  7. MEK inhibition enhances presentation of targetable MHC-I tumor antigens in mutant melanomas.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Review
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  11. Article
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  13. Article
  14. Article
  15. Article
  16. Antibody-based Delivery of TNF to the Tumor Neovasculature Potentiates the Therapeutic Activity of a Peptide Anticancer Vaccine.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  17. Article
  18. Identifying neoantigens for use in immunotherapy.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  19. The role of proteomics in the age of immunotherapies.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  20. 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

4 authors at 2 institutions in 1 country.

Andreas GlogerInstitute of Pharmaceutical Sciences, ETH Zurich, 8093, Zurich, Switzerland.
Danilo RitzPhilochem AG, Libernstrasse 3, 8112, Otelfingen, Switzerland.
Tim FugmannPhilochem AG, Libernstrasse 3, 8112, Otelfingen, Switzerland. tim.fugmann@philochem.ch.
Dario NeriInstitute of Pharmaceutical Sciences, ETH Zurich, 8093, Zurich, Switzerland. neri@pharma.ethz.ch.
ETH Zurich · CHPhilochem (Switzerland) · CH

Funding

European Research Council 670603Swiss National Science Foundation 163479
6 · The paper itself

Abstract

Melanoma is one of the most immunogenic tumors, and extensive lists of potential tumor rejection antigens have been collected during the last decades. By isolating human leukocyte antigen (HLA) class I complexes from five melanoma cell lines (FM-82, FM-93/2, Mel-624, MeWo and SK-Mel-5) and sequencing HLA-eluted peptides by mass spectrometry, we identified over 10,000 unique peptides with high confidence. The majority of the peptides were 8-11 amino acids in length and were predicted to bind to the respective HLA alleles. Over 250 epitopes, corresponding to previously described tumor-associated antigens, were identified, suggesting that HLA peptidome analysis may facilitate the characterization of putative tumor rejection antigens. MeWo and SK-Mel-5 cell lines were further interrogated for neo-epitopes, revealing one peptide from MeWo cells carrying an amino acid mutation. We also observed a remarkable overlap between A*03:01 peptides eluted from Mel-624 cells and A*03:01 peptides recovered from soluble HLA complexes purified from two melanoma patients, shedding light on the similarity of the HLA peptidome in cell lines and in patient-derived material. The reliable characterization of the HLA class I peptidome in melanoma promises to facilitate the identification of tumor rejection antigens and the development of immunotherapeutic strategies.

Indexed as

AllelesAntigens, NeoplasmCell Line, TumorCytotoxicity, ImmunologicEpitope MappingEpitopes, T-LymphocyteHistocompatibility Antigens Class IHLA AntigensHumansImmunotherapyMass SpectrometryMelanomaPeptidesProtein BindingT-Lymphocytes, CytotoxicAntigens, NeoplasmEpitopes, T-LymphocyteHistocompatibility Antigens Class IHLA AntigensPeptidesHLAImmunocaptureImmunopeptidomeMass spectrometryMelanomaTumor-associated antigen

Identifiers

PMID27600516
PMCPMC5509013
OpenAlexW2509527114

What OpenQuestion holds

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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.