Evidence map›Paper›PMID 25198515›Full record

ArticlePloS one2014

Inhibition of H3K9 methyltransferase G9a repressed cell proliferation and induced autophagy in neuroblastoma cells.

Xiao-Xue Ke, Dunke Zhang, Shunqin Zhu, Qingyou Xia, Zhonghuai Xiang, Hongjuan Cui

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.8field-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

48 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Discovery of the First-in-Class G9a/GLP PROTAC Degrader.Journal of medicinal chemistry · 2024
    Article
  5. Article
  6. Discovery of the First-in-class G9a/GLP PROTAC Degrader.bioRxiv : the preprint server for biology · 2024
    Article
  7. Histone Methyltransferases G9a/International journal of molecular sciences · 2023
    Article
  8. Insight into autophagy in platinum resistance of cancer.International journal of clinical oncology · 2023
    Review
  9. Article
  10. Article
  11. EHMT2/G9a as an Epigenetic Target in Pediatric and Adult Brain Tumors.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Review
  14. P53-regulated autophagy and its impact on drug resistance and cell fate.Cancer drug resistance (Alhambra, Calif.) · 2021
    Article
  15. Review
  16. Review
  17. Targeting autophagy in neuroblastoma.World journal of pediatric surgery · 2020
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Xiao-Xue KeState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Dunke ZhangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Shunqin ZhuState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Qingyou XiaState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Zhonghuai XiangState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
State Key Laboratory of Silkworm Genomic BiologySouthwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone methylation plays an important role in gene transcription and chromatin organization and is linked to the silencing of a number of critical tumor suppressor genes in tumorigenesis. G9a is a histone methyltransferase (HMTase) for histone H3 lysine 9. In this study, we investigated the role of G9a in neuroblastoma tumor growth together with the G9a inhibitor BIX01294. The exposure of neuroblastoma cells to BIX01294 resulted in the inhibition of cell growth and proliferation, and BIX01294 treatment resulted in the inhibition of the tumorigenicity of neuroblastoma cells in NOD/SCID mice. Therefore, G9a may be a potential therapeutic target in neuroblastoma. Moreover, we found several specific characteristics of autophagy after BIX01294 treatment, including the appearance of membranous vacuoles and microtubule-associated protein light chain 3 (LC3B). Similar results were observed in G9a-knockdown cells. In conclusion, our results demonstrated that G9a is a prognostic marker in neuroblastoma, and revealed a potential role of G9a in regulating the autophagy signaling pathway in neuroblastoma.

Indexed as

AutophagyCell ProliferationAnimalsCell Line, TumorFemaleFluorescent Antibody TechniqueHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHumansMiceMice, Inbred NODMice, SCIDNeuroblastomaHistone-Lysine N-MethyltransferaseHistone Methyltransferases

Identifiers

PMID25198515
PMCPMC4157855
OpenAlexW2068451609

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.