Evidence map›Paper›PMID 27294158›Full record

ReviewJournal of immunology research2016

NK Cells, Tumor Cell Transition, and Tumor Progression in Solid Malignancies: New Hints for NK-Based Immunotherapy?

Claudia Cantoni, Leticia Huergo-Zapico, Monica Parodi, Marco Pedrazzi, Maria Cristina Mingari, Alessandro Moretta, Bianca Sparatore, Segundo Gonzalez, Daniel Olive, Cristina Bottino and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of immunology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. The clinicopathological and prognostic value of programmed death-ligand 1 in colorectal cancer: a meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Pooled it
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  5. Targeting Cancer: Microenvironment and Immunotherapy Innovations.International journal of molecular sciences · 2024
    Review
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  19. EZH2 inhibits NK cell-mediated antitumor immunity by suppressing CXCL10 expression in an HDAC10-dependent manner.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

12 authors at 5 institutions in 3 countries.

Claudia CantoniDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genova, Italy; Istituto Giannina Gaslini, 16147 Genova, Italy.ORCID 0000-0001-6471-1424
Leticia Huergo-ZapicoIRCCS AOU San Martino-IST, 16132 Genova, Italy.
Monica ParodiIRCCS AOU San Martino-IST, 16132 Genova, Italy.
Marco PedrazziDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy.
Maria Cristina MingariDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genova, Italy; IRCCS AOU San Martino-IST, 16132 Genova, Italy.
Alessandro MorettaDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genova, Italy.ORCID 0000-0002-7116-426X
Bianca SparatoreDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genova, Italy.
Segundo GonzalezDepartment of Functional Biology, IUOPA, University of Oviedo, 33006 Oviedo, Spain.
Daniel OliveU1068, CRCM, Immunity and Cancer, INSERM, 1312 Marseille, France.
Cristina BottinoDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Istituto Giannina Gaslini, 16147 Genova, Italy.
Roberta CastriconiDepartment of Experimental Medicine (DIMES), University of Genoa, 16132 Genova, Italy; Center of Excellence for Biomedical Research (CEBR), University of Genoa, 16132 Genova, Italy.ORCID 0000-0003-2806-1115
Massimo VitaleIRCCS AOU San Martino-IST, 16132 Genova, Italy.ORCID 0000-0001-5372-7885
Ospedale Policlinico San Martino · ITUniversity of Genoa · ITIstituto Giannina Gaslini · ITInserm · FRUniversidad de Oviedo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several evidences suggest that NK cells can patrol the body and eliminate tumors in their initial phases but may hardly control established solid tumors. Multiple factors, including the transition of tumor cells towards a proinvasive/prometastatic phenotype, the immunosuppressive effect of the tumor microenvironment, and the tumor structure complexity, may account for limited NK cell efficacy. Several putative mechanisms of NK cell suppression have been defined in these last years; conversely, the cross talk between NK cells and tumor cells undergoing different transitional phases remains poorly explored. Nevertheless, recent in vitro studies and immunohistochemical analyses on tumor biopsies suggest that NK cells could not only kill tumor cells but also influence their evolution. Indeed, NK cells may induce tumor cells to change the expression of HLA-I, PD-L1, or NKG2D-L and modulate their susceptibility to the immune response. Moreover, NK cells may be preferentially located in the borders of tumor masses, where, indeed, tumor cells can undergo Epithelial-to-Mesenchymal Transition (EMT) acquiring prometastatic phenotype. Finally, the recently highlighted role of HMGB1 both in EMT and in amplifying the recruitment of NK cells provides further hints on a possible effect of NK cells on tumor progression and fosters new studies on this issue.

Indexed as

ImmunotherapyAnimalsB7-H1 AntigenCytotoxicity, ImmunologicDisease ProgressionEpithelial-Mesenchymal TransitionHLA AntigensHMGB1 ProteinHumansImmune ToleranceKiller Cells, NaturalNeoplasm MetastasisNeoplasmsNK Cell Lectin-Like Receptor Subfamily KTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanHLA AntigensHMGB1 ProteinHMGB1 protein, humanKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID27294158
PMCPMC4880686
OpenAlexW2352290668

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.