Evidence map›Paper›PMID 34233181›Full record

ArticleCell reports2021

Identification of a class of non-conventional ER-stress-response-derived immunogenic peptides.

Alessia Melacarne, Valentina Ferrari, Luca Tiraboschi, Michele Mishto, Juliane Liepe, Marina Aralla, Laura Marconato, Michela Lizier, Chiara Pozzi, Offer Zeira and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. Article
  9. Immunogenic cell stress and death.Nature immunology · 2022
    Review
  10. 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

12 authors at 7 institutions in 3 countries.

Alessia MelacarneIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy.
Valentina FerrariHumanitas University, Department of Biomedical Sciences, Via Rita Levi Montalcini, 20072 Pieve Emanuele, Milan, Italy.
Luca TiraboschiIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy.
Michele MishtoKing's College London, Centre for Inflammation Biology and Cancer Immunology, Peter Gorer Department of Immunobiology, Great Maze Pond, SE1 1UL London, UK; Francis Crick Institute, NW1 1AT London, UK.
Juliane LiepeMax-Planck-Institute for Biophysical Chemistry, Am Faßberg 11, 37077 Göttingen, Germany.
Marina ArallaPronto Soccorso Veterinario Laudense, Via Milano 22, 26900 Lodi, Italy.
Laura MarconatoUniversity of Bologna, Department of Veterinary Medical Science, via Tolara di Sopra, 40064 Ozzano dell'Emilia, Bologna, Italy.
Michela LizierIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy.
Chiara PozziIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy.
Offer ZeiraSan Michele Veterinary Hospital, via I maggio 26838 Tavazzano con Villavesco, Lodi, Italy.
Giuseppe PennaIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy.
Maria RescignoIRCCS Humanitas Research Hospital, via Manzoni 56, 20089 Rozzano, Milan, Italy; Humanitas University, Department of Biomedical Sciences, Via Rita Levi Montalcini, 20072 Pieve Emanuele, Milan, Italy. Electronic address: maria.rescigno@hunimed.eu.
IRCCS Humanitas Research Hospital · ITHumanitas University · ITCasa di Cura San Michele · ITMax Planck Institute for Biophysical Chemistry · DEStazione Sperimentale del Vetro · ITThe Francis Crick Institute · GBUniversity of Bologna · IT

Funding

Cancer Research UK 29686Cancer Research UK A29686Cancer Research UK C67500
6 · The paper itself

Abstract

Efforts to overcome resistance to immune checkpoint blockade therapy have focused on vaccination strategies using neoepitopes, although they cannot be applied on a large scale due to the "private" nature of cancer mutations. Here, we show that infection of tumor cells with Salmonella induces the opening of membrane hemichannels and the extracellular release of proteasome-generated peptides by the exacerbation of endoplasmic reticulum (ER) stress. Peptides released by cancer cells foster an antitumor response in vivo, both in mice bearing B16F10 melanomas and in dogs suffering from osteosarcoma. Mass spectrometry analysis on the supernatant of human melanoma cells revealed 12 peptides capable of priming healthy-donor CD8

Indexed as

Endoplasmic Reticulum StressPeptidesAmino Acid SequenceAnimalsCD8-Positive T-LymphocytesCell Line, TumorCell MembraneDogsFemaleHumansLymphocyte ActivationMaleMelanocytesMelanoma, ExperimentalMiceMice, Inbred C57BLPeptidesProteasome Endopeptidase ComplexcancerER-stress responseimmunotherapySalmonellatumor antigensvaccine

Identifiers

PMID34233181
PMCPMC8278487
OpenAlexW3181895799

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.