Evidence map›Paper›PMID 38985879›Full record

ArticleScience advances2024

Microproteins encoded by noncanonical ORFs are a major source of tumor-specific antigens in a liver cancer patient meta-cohort.

Marta E Camarena, Patrick Theunissen, Marta Ruiz, Jorge Ruiz-Orera, Beatriz Calvo-Serra, Robert Castelo, Carla Castro, Pablo Sarobe, Puri Fortes, Júlia Perera-Bel and 1 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Review
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  11. Article
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  14. Microproteins: Uncovering Hidden Layers of the Proteome.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Ins and outs of IRES elements: function and significance.Biochemical Society transactions · 2025
    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

11 authors.

Marta E CamarenaHospital del Mar Research Institute, Barcelona, Spain.ORCID 0000-0001-9319-6388
Patrick TheunissenCenter for Applied Medical Research (CIMA), University of Navarra (UNAV), Pamplona, Spain.ORCID 0000-0002-6009-3574
Marta RuizCenter for Applied Medical Research (CIMA), University of Navarra (UNAV), Pamplona, Spain.
Jorge Ruiz-OreraMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), 13125 Berlin, Germany.ORCID 0000-0002-8317-0034
Beatriz Calvo-SerraDepartment of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.ORCID 0000-0002-7614-396X
Robert CasteloDepartment of Medicine and Life Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain.ORCID 0000-0003-2229-4508
Carla CastroCenter for Applied Medical Research (CIMA), University of Navarra (UNAV), Pamplona, Spain.ORCID 0009-0006-6825-2329
Pablo SarobeCenter for Applied Medical Research (CIMA), University of Navarra (UNAV), Pamplona, Spain.
Puri FortesCenter for Applied Medical Research (CIMA), University of Navarra (UNAV), Pamplona, Spain.ORCID 0000-0001-7571-6220
Júlia Perera-BelHospital del Mar Research Institute, Barcelona, Spain.ORCID 0000-0002-6809-132X
M Mar AlbàHospital del Mar Research Institute, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of tumor-specific antigens during cancer progression can trigger an immune response against the tumor. Here, we investigate if microproteins encoded by noncanonical open reading frames (ncORFs) are a relevant source of tumor-specific antigens. We analyze RNA sequencing data from 117 hepatocellular carcinoma (HCC) tumors and matched healthy tissue together with ribosome profiling and immunopeptidomics data. Combining human leukocyte antigen-epitope binding predictions and experimental validation experiments, we conclude that around 40% of the tumor-specific antigens in HCC are likely to be derived from ncORFs, including two peptides that can trigger an immune response in humanized mice. We identify a subset of 33 tumor-specific long noncoding RNAs expressing novel cancer antigens shared by more than 10% of the HCC samples analyzed, which, when combined, cover a large proportion of the patients. The results of the study open avenues for extending the range of anticancer vaccines.

Indexed as

Antigens, NeoplasmCarcinoma, HepatocellularLiver NeoplasmsOpen Reading FramesAnimalsCohort StudiesGene Expression Regulation, NeoplasticHumansMiceMicropeptidesRNA, Long NoncodingAntigens, NeoplasmMicropeptidesRNA, Long Noncoding

Identifiers

PMID38985879
PMCPMC11235171

What OpenQuestion holds

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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.