Evidence map›Paper›PMID 34552178›Full record

ArticleCommunications biology2021

Single-cell profiling defines the prognostic benefit of CD39

Agnese Losurdo, Caterina Scirgolea, Giorgia Alvisi, Jolanda Brummelman, Valentina Errico, Luca Di Tommaso, Karolina Pilipow, Federico Simone Colombo, Bethania Fernandes, Clelia Peano and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

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  8. Frontiers in molecular biosciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Agnese Losurdo *Laboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy. agnese.losurdo@cancercenter.humanitas.it.
Caterina Scirgolea *Laboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0001-9213-5532
Giorgia AlvisiLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Jolanda BrummelmanLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0003-3581-4816
Valentina ErricoBreast Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Luca Di TommasoDepartment of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Karolina PilipowLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Federico Simone ColomboHumanitas Flow Cytometry Core, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0003-4480-3481
Bethania FernandesDepartment of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0002-4327-1586
Clelia PeanoGenomic Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0001-7055-3629
Alberto TestoriBreast Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Corrado TinterriBreast Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Massimo RoncalliDepartment of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Armando SantoroMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0003-1709-9492
Emilia Maria Cristina MazzaLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.ORCID http://orcid.org/0000-0003-2424-3640
Enrico LugliLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy. enrico.lugli@humanitasresearch.it.ORCID http://orcid.org/0000-0002-1964-7678
IRCCS Humanitas Research Hospital · ITHumanitas University · ITInstitute of Genetic and Biomedical Research · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Luminal-like breast cancer (BC) constitutes the majority of BC subtypes, but, differently from highly aggressive triple negative BC, is poorly infiltrated by the immune system. The quality of the immune infiltrate in luminal-like BCs has been poorly studied, thereby limiting further investigation of immunotherapeutic strategies. By using high-dimensional single-cell technologies, we identify heterogeneous behavior within the tissue-resident memory CD8+ T (Trm) cells infiltrating luminal-like tumors. A subset of CD127- CD39

Indexed as

ApyraseBreast NeoplasmsCD8-Positive T-LymphocytesHumansPrognosisSingle-Cell AnalysisApyraseENTPD1 protein, human

Identifiers

PMID34552178
PMCPMC8458450
OpenAlexW3199822463

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.