Evidence map›Paper›PMID 40912740›Full record

ArticleJournal for immunotherapy of cancer2025

High transposable element expression in sarcomas is associated with increased immune infiltrates and improved outcomes including after immunotherapy.

Benjamin A Nacev, Martina Bradic, Hyung Jun Woo, Allison L Richards, Ciara M Kelly, Mark A Dickson, Mrinal M Gounder, Mary L Keohan, Ping Chi, Sujana Movva and 12 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

22 authors.

Benjamin A Nacev *Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA nacevba@upmc.edu.ORCID http://orcid.org/0000-0003-4991-2492
Martina Bradic *Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Hyung Jun WooMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Allison L RichardsMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Ciara M KellyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mark A DicksonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mrinal M GounderDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mary L KeohanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Ping ChiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sujana MovvaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-6569-6606
Robert G MakiDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-9853-2528
Emily K SlotkinWeill Cornell Medical College, New York, New York, USA.
Evan RosenbaumDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-7499-1279
Viswatej AvutuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Jason E ChanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0003-0552-8544
Lauren B BanksDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Travis AdamsonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Samuel SingerDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Cristina R AntonescuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
William D TapDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mark Ta Donoghue *Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sandra P D'Angelo *Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID http://orcid.org/0000-0002-3736-3783

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 1988 to 2026
$158.0M
Understanding and targeting MAPK pathway activation in NF1-deficient malignant peripheral nerve sheath tumor (MPNST)U01CA252048 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHI, PING · 2021 to 2025
$3.1M
Harnessing double stranded-RNA (dsRNA)-response and anti-tumor effect in PRC2-inactivated cancerR01CA280657 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Ping Chi · 2023 to 2026
$2.9M
Elucidating and targeting the effects of oncogenic histone mutationsK08CA245212 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NACEV, BENJAMIN A · 2019 to 2023
$1.4M
NCI NIH HHS K08 CA245212NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA047904NCI NIH HHS R01 CA280657NCI NIH HHS U01 CA252048
6 · The paper itself

Abstract

backgroundResponse to immune checkpoint inhibition (ICI) in sarcomas is overall low and heterogeneous. Understanding determinants of ICI outcomes may improve efficacy and patient selection. Thus, we investigated whether the expression of transposable elements (TEs), which are epigenetically silenced and can stimulate antitumor immunity, influence ICI outcomes and immune infiltrates in common sarcoma subtypes.

methodsWe used transcriptomic data to assign immune enhanced versus immune depleted status to 67 pretreatment and on-treatment biopsies of sarcomas from patients treated on ICI trials, along with additional cohorts from The Cancer Genome Atlas (TCGA) and an independent ICI trial (SARC028). A machine learning technique (lasso-penalized logistic regression) controlled for sarcoma subtype was used to determine if TE and epigenetic regulatory gene expression predict immune infiltrates. Correlations between top features in these models and sarcoma immune infiltrates, immune pathway expression, and clinical outcomes were explored.

resultsExpression of TEs and epigenetic regulators significantly predicted immune enhanced status. TE subfamilies and Ikaros family zinc finger 1 (

conclusionsTE and

Indexed as

DNA Transposable ElementsImmunotherapySarcomaFemaleGene Expression Regulation, NeoplasticHumansMaleDNA Transposable ElementsImmune Checkpoint InhibitorSarcoma

Identifiers

PMID40912740
PMCPMC12414182

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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.