Evidence map›Paper›PMID 38023136›Full record

ArticleFrontiers in oncology2023

A transcriptional evaluation of the melanoma and squamous cell carcinoma TIL compartment reveals an unexpected spectrum of exhausted and functional T cells.

Cheryl M Cameron, Brian Richardson, Jackelyn B Golden, Yee Peng Phoon, Banumathi Tamilselvan, Lukas Pfannenstiel, Samjhana Thapaliya, Gustavo Roversi, Xing-Huang Gao, Leah L Zagore and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Cheryl M CameronDepartment of Nutrition, Case Western Reserve University, Cleveland, OH, United States.
Brian RichardsonDepartment of Nutrition, Case Western Reserve University, Cleveland, OH, United States.
Jackelyn B GoldenDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, United States.
Yee Peng PhoonDepartment of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, United States.
Banumathi TamilselvanDepartment of Nutrition, Case Western Reserve University, Cleveland, OH, United States.
Lukas PfannenstielDepartment of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, United States.
Samjhana ThapaliyaDepartment of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, United States.
Gustavo RoversiDepartment of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, United States.
Xing-Huang GaoDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, United States.
Leah L ZagoreDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, United States.
Mark J CameronDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, United States.
Brian R GastmanDepartment of Inflammation and Immunity, Cleveland Clinic, Cleveland, OH, United States.

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Amar Desai · 1987 to 2026
$142.3M
NCI NIH HHS P30 CA043703
6 · The paper itself

Abstract

Introduction: Significant heterogeneity exists within the tumor-infiltrating CD8 T cell population, and exhausted T cells harbor a subpopulation that may be replicating and may retain signatures of activation, with potential functional consequences in tumor progression. Dysfunctional immunity in the tumor microenvironment is associated with poor cancer outcomes, making exploration of these exhausted T cell subpopulations critical to the improvement of therapeutic approaches. Methods: To investigate mechanisms associated with terminally exhausted T cells, we sorted and performed transcriptional profiling of CD8 Results: We identified novel dysregulated pathways in CD8 Discussion: Based on bioinformatic integration of immunophenotypic data and network analysis, we propose unexpected targets for therapies to rescue the immune response to tumors in melanoma.

Indexed as

immune checkpoint receptormelanomaRNAseqT cellstumor-infiltrating cells

Identifiers

PMID38023136
PMCPMC10643547

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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.