Evidence map›Paper›PMID 30382083›Full record

ArticleNature communications2018

PRMT2 links histone H3R8 asymmetric dimethylation to oncogenic activation and tumorigenesis of glioblastoma.

Feng Dong, Qian Li, Chao Yang, Dawei Huo, Xing Wang, Chunbo Ai, Yu Kong, Xiaoyu Sun, Wen Wang, Yan Zhou and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

67 citing papers in PubMed, 121 citations in OpenAlex.

  1. oHSV-1-modulated mVirology journal · 2026
    Article
  2. Review
  3. Dynamic regulation of histone arginine methylation in anoxic freshwater turtles.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Epigenetic regulation of cancer stemness.Signal transduction and targeted therapy · 2025
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

7 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

16 authors at 6 institutions in 1 country.

Feng DongDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Qian LiDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Chao YangDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Dawei HuoDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Xing WangDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Chunbo AiDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Yu KongDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Xiaoyu SunDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China.
Wen WangHubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, 430072, China.
Yan ZhouHubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, 430072, China.ORCID http://orcid.org/0000-0002-2713-4442
Xing LiuDepartment of Neuropathology, Beijing Neurosurgical Institute, Capital Medical University, 6 Tiantanxi Li, Beijing, 100050, China.
Wei LiDepartment of Pathology, Tianjin Nankai Hospital, Tianjin, 300100, China.
Weiwei GaoSchool of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Wen LiuSchool of Pharmaceutical Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Chunsheng KangDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, 300052, China. kang97061@gmail.com.
Xudong WuDepartment of Cell Biology, Tianjin Medical University, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Qixiangtai Road 22, Tianjin, 300070, China. wuxudong@tmu.edu.cn.
Tianjin Medical University · CNTianjin Medical University General Hospital · CNWuhan University · CNXiamen University · CNCapital Medical University · CNTianjin Nankai Hospital · CN

Funding

Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2017YFA0504102Natural Science Foundation of Tianjin City (Natural Science Foundation of Tianjin) 17JCZDJC35200
6 · The paper itself

Abstract

Transcriptional deregulation has a vital role in glioblastoma multiforme (GBM). Thus, identification of epigenetic modifiers essential for oncogenic transcriptional programs is a key to designing effective therapeutics for this deadly disease. Here we report that Protein Arginine Methyltransferase 2 (PRMT2) is highly expressed in GBM and correlated with poor prognosis. The silencing or inactivation of PRMT2 inhibits GBM cell growth and glioblastoma stem cell self-renewal in vitro, and suppresses orthotopic tumor growth, accompanied with significant deregulation of genes mainly associated with cell cycle progression and pathways in cancer. Mechanistically PRMT2 is responsible for H3R8 asymmetric methylation (H3R8me2a), whose enrichment at promoters and enhancers is closely correlated with known active histone marks and is required for the maintenance of target gene expression. Together, this study demonstrates that PRMT2 acts as a transcriptional co-activator for oncogenic gene expression programs in GBM pathogenesis and provides a rationale for PRMT2 targeting in aggressive gliomas.

Indexed as

OncogenesArginineBrain NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationCell Self RenewalEnhancer Elements, GeneticGene Expression Regulation, NeoplasticGlioblastomaHistonesHumansIntracellular Signaling Peptides and ProteinsMethylationPromoter Regions, GeneticProtein-Arginine N-MethyltransferasesArginineHistonesIntracellular Signaling Peptides and ProteinsPRMT2 protein, humanProtein-Arginine N-Methyltransferases

Identifiers

PMID30382083
PMCPMC6208368
OpenAlexW2898545092

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.