Evidence map›Paper›PMID 31745090›Full record

ArticleNature communications2019

Transposable element expression in tumors is associated with immune infiltration and increased antigenicity.

Yu Kong, Christopher M Rose, Ashley A Cass, Alexander G Williams, Martine Darwish, Steve Lianoglou, Peter M Haverty, Ann-Jay Tong, Craig Blanchette, Matthew L Albert and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 1% 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

183 citing papers in PubMed, 1 synthesis or guideline pooled it, 286 citations in OpenAlex.

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  17. Association of Circulating T Cell and Tumor Microenvironment Profiles with Immune Checkpoint Blockade Outcomes in Sarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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123 more citing papers are in PubMed but not listed here.

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

15 authors at 3 institutions in 1 country.

Yu KongDepartment of Genetics and Center for Epigenomics, Albert Einstein College of Medicine, New York, 10461, USA.
Christopher M RoseGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0002-7502-3368
Ashley A CassDepartment of Bioinformatics Interdepartmental Program, University of California at Los Angeles, Los Angeles, CA, USA.
Alexander G WilliamsGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0002-5110-1245
Martine DarwishGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Steve LianoglouGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Peter M HavertyGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Ann-Jay TongGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Craig BlanchetteGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Matthew L AlbertGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0001-7285-6973
Ira MellmanGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Richard BourgonGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.ORCID http://orcid.org/0000-0002-5890-4374
John GreallyDepartment of Genetics and Center for Epigenomics, Albert Einstein College of Medicine, New York, 10461, USA.ORCID http://orcid.org/0000-0001-6069-7960
Suchit JhunjhunwalaGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Haiyin Chen-HarrisGenentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA. haiyin@argonautgenomics.com.ORCID http://orcid.org/0000-0002-3948-3068
Albert Einstein College of Medicine · USParagon Genomics (United States) · USUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Profound global loss of DNA methylation is a hallmark of many cancers. One potential consequence of this is the reactivation of transposable elements (TEs) which could stimulate the immune system via cell-intrinsic antiviral responses. Here, we develop REdiscoverTE, a computational method for quantifying genome-wide TE expression in RNA sequencing data. Using The Cancer Genome Atlas database, we observe increased expression of over 400 TE subfamilies, of which 262 appear to result from a proximal loss of DNA methylation. The most recurrent TEs are among the evolutionarily youngest in the genome, predominantly expressed from intergenic loci, and associated with antiviral or DNA damage responses. Treatment of glioblastoma cells with a demethylation agent results in both increased TE expression and de novo presentation of TE-derived peptides on MHC class I molecules. Therapeutic reactivation of tumor-specific TEs may synergize with immunotherapy by inducing inflammation and the display of potentially immunogenic neoantigens.

Indexed as

Antigens, NeoplasmCell Line, TumorComputational BiologyDNA MethylationDNA Transposable ElementsGene ExpressionGene Expression ProfilingHumansImmunotherapyNeoplasmsSequence Analysis, RNAAntigens, NeoplasmDNA Transposable Elements

Identifiers

PMID31745090
PMCPMC6864081
OpenAlexW2989996227

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.