Evidence map›Paper›PMID 35246593›Full record

ArticleScientific reports2022

Extrachromosomal DNA formation enables tumor immune escape potentially through regulating antigen presentation gene expression.

Tao Wu, Chenxu Wu, Xiangyu Zhao, Guangshuai Wang, Wei Ning, Ziyu Tao, Fuxiang Chen, Xue-Song Liu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Targeting extrachromosomal DNA in human cancers.Nature reviews. Drug discovery · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Extrachromosomal DNA and cancer: function, formation, and clinical implications.Journal of experimental & clinical cancer research : CR · 2026
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Interferon Epsilon Loss Is Elusive 9p21 Link to Immune-Cold Tumors, Resistant to Immune Checkpoint Therapy, and Endogenous CXCL9/10 Induction.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Review
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Tao Wu *School of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Chenxu Wu *School of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Xiangyu ZhaoSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Guangshuai WangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Wei NingSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Ziyu TaoSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China.
Fuxiang ChenDepartment of Clinical Immunology, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, People's Republic of China.
Xue-Song LiuSchool of Life Science and Technology, ShanghaiTech University, Shanghai, 201203, People's Republic of China. liuxs@shanghaitech.edu.cn.
ShanghaiTech University · CNChinese Academy of Sciences · CNShanghai Ninth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extrachromosomal DNA (ecDNA) is a type of circular and tumor specific genetic element. EcDNA has been reported to display open chromatin structure, facilitate oncogene amplification and genetic material unequal segregation, and is associated with poor cancer patients' prognosis. The ability of immune evasion is a typical feature for cancer progression, however the tumor intrinsic factors that determine immune evasion remain poorly understood. Here we show that the presence of ecDNA is associated with markers of tumor immune evasion, and obtaining ecDNA could be one of the mechanisms employed by tumor cells to escape immune surveillance. Tumors with ecDNA usually have comparable TMB and neoantigen load, however they have lower immune cell infiltration and lower cytotoxic T cell activity. The microenvironment of tumors with ecDNA shows increased immune-depleted, decreased immune-enriched fibrotic types. Both MHC class I and class II antigen presentation genes' expression are decreased in tumors with ecDNA, and this could be the underlying mechanism for ecDNA associated immune evasion. This study provides evidence that ecDNA formation is an immune escape mechanism for cancer cells.

Indexed as

DNA, B-FormNeoplasmsAntigen PresentationGene ExpressionHumansOncogenesTumor EscapeTumor MicroenvironmentDNA, B-Form

Identifiers

PMID35246593
PMCPMC8897507
OpenAlexW4214857266

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.