Evidence map›Paper›PMID 40161761›Full record

ArticlebioRxiv : the preprint server for biology2025

Shared PRAME Epitopes are T-Cell Targets in NUT Carcinoma.

Jeffrey L Jensen, Sara K Peterson, Maria Sambade, Jessica R Alley, Shawn Yu, Tomoaki Kinjo, Sarah N Bennett, Steven P Vensko, Mitra Shabrang, Johnathan D DeBetta and 13 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Maria Sambade
Jessica R Alley
Shawn Yu
Tomoaki Kinjo
Steven P Vensko
Mitra Shabrang
Johnathan D DeBetta
Julie K Geyer
Brandon A Price
Kwangok P Nickel
Randall J Kimple
Laura E Herring
Christopher A French
Jared Weiss
Benjamin G Vincent

Funding

Gvl mHA Specific T Cell Responses Prevent AML Relapse Following Allogeneic Stem Cell Transplantation.R37CA247676 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI VINCENT, BENJAMIN G · 2020 to 2025
$3.6M
Improving the translational value of head and neck cancer patient-in-mouse modelsR37CA255330 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Randall J. Kimple · 2021 to 2026
$3.5M
UNC Immunotherapy Training Grant (IM-TAG)T32CA285257 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jonathan S. Serody · 2023 to 2026
$668k
NCI NIH HHS R37 CA247676NCI NIH HHS R37 CA255330NCI NIH HHS T32 CA285257
6 · The paper itself

Abstract

Background: NUT carcinoma is a rare but highly lethal solid tumor without an effective standard of care. NUT carcinoma is caused by bromodomain-containing Methods: We integrated genomics, computational antigen prediction software, targeted immunopeptidomics using single- and double-labeled peptide standards, and gain/loss-of-function genetic experiments on a panel of cell lines (N=5), a patient derived xenograft, a tissue microarray (N=77), and patient samples from the Tempus AI Sequencing Database harboring evidence of Results: We identified Conclusions: What is already known on this topic: NUT carcinoma is a devastating malignancy that is recalcitrant to cytotoxic chemotherapy, T-cell checkpoint blockade, and targeted therapies in the form of bromodomain inhibitors. What this study adds: NUT carcinoma tumors are high in the cancer/testis gene How this study might affect research practice or policy: Our results argue for phase I/II clinical trials testing PRAME immunotherapies like brenetafusp or anzutresgene autoleucel in

Identifiers

PMID40161761
PMCPMC11952323

What Socratic holds

Textmetadata
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 Socratic graph.