Evidence map›Paper›PMID 35163710›Full record

ArticleInternational journal of molecular sciences2022

EZH2-CCF-cGAS Axis Promotes Breast Cancer Metastasis.

Dandan Duan, Mengjie Shang, Yanxu Han, Jiayuan Liu, Jiwei Liu, Sun Hyok Kong, Jingyao Hou, Baiqu Huang, Jun Lu, Yu Zhang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The role of HMGA1 in genome stability: Implications in human cancer.Cellular and molecular life sciences : CMLS · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Role of PRMT1 and PRMT5 in Breast Cancer.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. How Does cGAS Avoid Sensing Self-DNA under Normal Physiological Conditions?International journal of molecular sciences · 2023
    Review
  20. 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

10 authors at 1 institution in 1 country.

Dandan DuanThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.ORCID 0000-0001-5145-9864
Mengjie ShangThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.
Yanxu HanThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.
Jiayuan LiuThe Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China.
Jiwei LiuSchool of Life Science and Technology, Inner Mongolia University of Science & Technology, Baotou 014010, China.
Sun Hyok KongThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.
Jingyao HouThe Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China.
Baiqu HuangThe Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China.
Jun LuThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.
Yu ZhangThe Key Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun 130024, China.ORCID 0000-0002-3702-6541
Northeast Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytoplasmic chromatin fragments (CCF) are recognized by the cytoplasmic DNA sensor cyclic GMP-AMP synthase (cGAS), which activates the cGAS-STING (cyclic GMP-AMP synthase-stimulator of interferon genes) pathway and promotes the production of inflammatory factors and breast cancer metastasis. However, the mechanisms by which CCF are formed in tumor cells and CCF activation cGAS promotes breast cancer metastasis remain unclear. Here, we report that the enhancer of zeste homolog 2 (EZH2) can promote the formation of CCF and activate the cGAS-STING pathway to promote breast cancer metastasis. Further research found that the EZH2-mediated CCF formation depended on high mobility group A1 (HMGA1), while the stability of EZH2 required ubiquitin-specific peptidase 7 (USP7), indicating that the EZH2-HMGA1-USP7 complex regulated CCF formation. Moreover, EZH2 can activate cGAS through CCF, requiring USP7 to deubiquitinate cGAS and stabilize cGAS. In vivo experimental results showed that EZH2 could promote breast cancer metastasis through CCF. Our findings highlight a new target for breast cancer metastasis. Targeting the EZH2-CCF-cGAS axis may be a potential therapeutic strategy for inhibiting breast cancer metastasis.

Indexed as

Breast NeoplasmsChromatinEnhancer of Zeste Homolog 2 ProteinNucleotidyltransferasesCutaneous Malignant MelanomaCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseFemaleHMGA1a ProteinHumansMelanomaMembrane ProteinsSignal TransductionSkin NeoplasmsUbiquitin-Specific Peptidase 7cGAS protein, humanChromatinCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHMGA1a ProteinMembrane ProteinsNucleotidyltransferasesUbiquitin-Specific Peptidase 7USP7 protein, humanbreast cancer metastasiscGAScytoplasmic chromatin fragmentsEZH2USP7

Identifiers

PMID35163710
PMCPMC8836657
OpenAlexW4210492618

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.