Evidence map›Paper›PMID 36032129›Full record

ReviewFrontiers in immunology2022

Innate lymphoid cells in early tumor development.

Kathrin Warner, Maryam Ghaedi, Douglas C Chung, Nicolas Jacquelot, Pamela S Ohashi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Kathrin WarnerPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Maryam GhaediPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Douglas C ChungPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Nicolas JacquelotPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Pamela S OhashiPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Princess Margaret Cancer Centre · CAUniversity Health Network · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate and adaptive immune cells monitor, recognize, and eliminate transformed cells. Innate lymphoid cells (ILCs) are innate counterparts of T cells that play a key role in many facets of the immune response and have a profound impact on disease states, including cancer. ILCs regulate immune responses by responding and integrating a wide range of signals within the local microenvironment. As primarily tissue-resident cells, ILCs are ideally suited to sense malignant transformation and initiate anti-tumor immunity. However, as ILCs have been associated with anti-tumor and pro-tumor activities in established tumors, they could potentially have dual functions during carcinogenesis by promoting or suppressing the malignant outgrowth of premalignant lesions. Here we discuss emerging evidence that shows that ILCs can impact early tumor development by regulating immune responses against transformed cells, as well as the environmental cues that potentially induce ILC activation in premalignant lesions.

Indexed as

Immunity, InnateNeoplasmsCarcinogenesisHumansLymphocytesTumor Microenvironmentcarcinogenesiscytokinesdamage associate molecular pattern (DAMP)immunosurveillanceinnate lymphoid cell (ILC)tumor developmenttumor immunity

Identifiers

PMID36032129
PMCPMC9411809
OpenAlexW4291165537

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.