Evidence map›Paper›PMID 34066087›Full record

ReviewInternational journal of molecular sciences2021

PD-1/PD-L1 in Cancer: Pathophysiological, Diagnostic and Therapeutic Aspects.

Enrico Munari, Francesca R Mariotti, Linda Quatrini, Pietro Bertoglio, Nicola Tumino, Paola Vacca, Albino Eccher, Francesco Ciompi, Matteo Brunelli, Guido Martignoni and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 6 pooled it
7.5field-weighted citation impact, top 2% 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

89 citing papers in PubMed, 6 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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  8. E3 Ubiquitin Ligase MDM2 Promotes Growth and CD8Journal of gastroenterology and hepatology · 2026
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29 more citing papers are in PubMed but not listed here.

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 6 institutions in 2 countries.

Enrico MunariPathology Unit, Department of Molecular and Translational Medicine, University of Brescia, 25100 Brescia, Italy.
Francesca R MariottiImmunology Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.ORCID 0000-0002-3421-6470
Linda QuatriniImmunology Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Pietro BertoglioDivision of Thoracic Surgery, IRCCS Maggiore Teaching Hospital and Sant'Orsola University Hospital, 40133 Bologna, Italy.ORCID 0000-0002-6267-0099
Nicola TuminoImmunology Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Paola VaccaImmunology Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Albino EccherPathology Unit, University and Hospital Trust of Verona, 37134 Verona, Italy.ORCID 0000-0002-9992-5550
Francesco CiompiComputational Pathology Group, Department of Pathology, Radboud University Medical Center, 6543 SH Nijmegen, The Netherlands.
Matteo BrunelliDepartment of Diagnostics and Public Health, University of Verona, 37134 Verona, Italy.
Guido MartignoniDepartment of Diagnostics and Public Health, University of Verona, 37134 Verona, Italy.
Giuseppe BoginaPathology Unit, IRCCS Sacro Cuore Don Calabria, 37024 Negrar di Valpolicella, Italy.ORCID 0000-0002-0311-2708
Lorenzo MorettaImmunology Area, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Bambino Gesù Children's Hospital · ITUniversity of Verona · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITOspedale Sacro Cuore Don Calabria · ITRadboud University Nijmegen · NLUniversity of Brescia · IT

Funding

Associazione Italiana per la Ricerca sul Cancro Id. 19920Associazione Italiana per la Ricerca sul Cancro (AIRC)-Special Program Metastatic disease: the key unmet need in oncology 5X1000 21147H2020 Marie Skłodowska-Curie Actions 800924
6 · The paper itself

Abstract

Immune evasion is a key strategy adopted by tumor cells to escape the immune system while promoting their survival and metastatic spreading. Indeed, several mechanisms have been developed by tumors to inhibit immune responses. PD-1 is a cell surface inhibitory receptor, which plays a major physiological role in the maintenance of peripheral tolerance. In pathological conditions, activation of the PD-1/PD-Ls signaling pathway may block immune cell activation, a mechanism exploited by tumor cells to evade the antitumor immune control. Targeting the PD-1/PD-L1 axis has represented a major breakthrough in cancer treatment. Indeed, the success of PD-1 blockade immunotherapies represents an unprecedented success in the treatment of different cancer types. To improve the therapeutic efficacy, a deeper understanding of the mechanisms regulating PD-1 expression and signaling in the tumor context is required. We provide an overview of the current knowledge of PD-1 expression on both tumor-infiltrating T and NK cells, summarizing the recent evidence on the stimuli regulating its expression. We also highlight perspectives and limitations of the role of PD-L1 expression as a predictive marker, discuss well-established and novel potential approaches to improve patient selection and clinical outcome and summarize current indications for anti-PD1/PD-L1 immunotherapy.

Indexed as

Molecular Targeted TherapyB7-H1 AntigenHumansImmune Checkpoint InhibitorsImmunotherapyNeoplasmsProgrammed Cell Death 1 ReceptorTumor EscapeB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorcancerglucocorticoidsimmunotherapyNK cellsPD-1PD-L1

Identifiers

PMID34066087
PMCPMC8151504
OpenAlexW3160380101

What OpenQuestion holds

Textmetadata
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.