Evidence map›Paper›PMID 29492219›Full record

ArticleOncotarget2018

PD-L1 expression in colorectal cancer defines three subsets of tumor immune microenvironments.

Anna Maria Valentini, Federica Di Pinto, Filomena Cariola, Vito Guerra, Gianluigi Giannelli, Maria Lucia Caruso, Michele Pirrelli

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.1field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

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  17. Role of PD-L1 in Gut Mucosa Tolerance and Chronic Inflammation.International journal of molecular sciences · 2020
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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

7 authors at 1 institution in 1 country.

Anna Maria ValentiniDepartment of Pathology, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Federica Di PintoDepartment of Pathology, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Filomena CariolaMedical Genetic Unit, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Vito GuerraDepartment of Epidemiology, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Gianluigi GiannelliNational Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Maria Lucia CarusoDepartment of Pathology, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Michele PirrelliDepartment of Pathology, National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, Italy.
Gastroenterology Hospital "Saverio de Bellis" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe investigated the PD-L1 expression in colorectal cancer (CRC) and in its microenvironment.

resultsPD-L1 was expressed in neoplastic cells (NCs) and tumor-infiltrating immune cells (IICs). All samples PD-L1+ on NCs were also on IICs. Three types of cancers could be grouped: group A(NCs-/ IICs-); group B (NCs-/ IICs+); group C (NCs+/IICs+). To group A belong tumors characterized by poorly immunogenic competence, poor immune response but massive granulocyte infiltrate, justifying the absence of PD-L1 as an immunoinhibitor receptor. To Group B probably belong more immunogenic CRCs, justifying the strong IICs-mediated immune response, and up-regulation of PD-L1 expression only on IICs. To group C belong CRCs probably characterized by a large amount of tumor neoantigens resulting in a marked infiltration of lymphocytes and PD-L1 upregulation also in NCs. MATERIALS AND

methodsSixty-three colorectal cancer specimens from a cohort of 61 patients were retrospectively reviewed. Thirty-seven MSS and 26 MSI-H CRCs enrolled in this study. Immunohistochemical staining to PD-L1 was performed by using MAb E1L3N.

conclusionsOur study calls attention to the importance to assess PD-L1 expression in tumor microenvironment also evaluating type and density of infiltrating immune cells to better stratify CRCs with different immunological patterns.

Indexed as

colorectal cancerimmunohistochemistrymicrosatellite instabilityPD-1PD-L1

Identifiers

PMID29492219
PMCPMC5823560
OpenAlexW2783967845

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Registered trials

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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.