Evidence map›Paper›PMID 24605112›Full record

ReviewFrontiers in immunology2014

The emerging immunological role of post-translational modifications by reactive nitrogen species in cancer microenvironment.

Francesco De Sanctis, Sara Sandri, Giovanna Ferrarini, Irene Pagliarello, Silvia Sartoris, Stefano Ugel, Ilaria Marigo, Barbara Molon, Vincenzo Bronte

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Trial
  2. Nitration in cancer signaling.Redox biology · 2026
    Review
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  8. Review
  9. MDSC: a new potential breakthrough in CAR-T therapy for solid tumors.Cell communication and signaling : CCS · 2024
    Review
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  11. Review
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  15. Article
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  19. Observational
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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

9 authors.

Francesco De SanctisImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Sara SandriImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Giovanna FerrariniImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Irene PagliarelloImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Silvia SartorisImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Stefano UgelImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.
Ilaria MarigoIstituto Oncologico Veneto, Istituto Di Ricovero e Cura a Carattere Scientifico , Padua , Italy.
Barbara MolonVenetian Institute of Molecular Medicine , Padua , Italy.
Vincenzo BronteImmunology Section, Department of Pathology and Diagnostics, University of Verona , Verona , Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Under many inflammatory contexts, such as tumor progression, systemic and peripheral immune response is tailored by reactive nitrogen species (RNS)-dependent post-translational modifications, suggesting a biological function for these chemical alterations. RNS modify both soluble factors and receptors essential to induce and maintain a tumor-specific immune response, creating a "chemical barrier" that impairs effector T cell infiltration and functionality in tumor microenvironment and supports the escape phase of cancer. RNS generation during tumor growth mainly depends on nitric oxide production by both tumor cells and tumor-infiltrating myeloid cells that constitutively activate essential metabolic pathways of l-arginine catabolism. This review provides an overview of the potential immunological and biological role of RNS-induced modifications and addresses new approaches targeting RNS either in search of novel biomarkers or to improve anti-cancer treatment.

Indexed as

cancerimmune escapemicroenvironmentnitrotyrosineRNS

Identifiers

PMID24605112
PMCPMC3932549

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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.