Evidence map›Paper›PMID 32183406›Full record

ArticleCells2020

STAT3 Inhibitor ODZ10117 Suppresses Glioblastoma Malignancy and Prolongs Survival in a Glioblastoma Xenograft Model.

Byung-Hak Kim, Haeri Lee, Cheol Gyu Park, Ae Jin Jeong, Song-Hee Lee, Kum Hee Noh, Jong Bae Park, Chung-Gi Lee, Sun Ha Paek, Hyunggee Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Immunotherapy in Glioblastoma.Cancer treatment and research · 2025
    Review
  9. Article
  10. Review
  11. Unraveling the complexity of STAT3 in cancer: molecular understanding and drug discovery.Journal of experimental & clinical cancer research : CR · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Recognition of a Novel Gene Signature for Human Glioblastoma.International journal of molecular sciences · 2022
    Article
  17. Article
  18. Article
  19. Article
  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

11 authors at 3 institutions in 1 country.

Byung-Hak KimDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID 0000-0001-7746-6616
Haeri LeeDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.
Cheol Gyu ParkDepartment of Biotechnology, School of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.
Ae Jin JeongDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.
Song-Hee LeeDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID 0000-0002-4208-261X
Kum Hee NohDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.
Jong Bae ParkDepartment of System Cancer Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang 10408, Korea.
Chung-Gi LeeCYTUS H&B Corporation, Cheongju 28159, Korea.ORCID 0000-0003-3821-1316
Sun Ha PaekDepartment of Neurosurgery, Seoul National University College of Medicine, Seoul 03080, Korea.
Hyunggee KimDepartment of Biotechnology, School of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.
Sang-Kyu YeDepartment of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Korea.
Seoul National University · KRKorea University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Constitutively activated STAT3 plays an essential role in the initiation, progression, maintenance, malignancy, and drug resistance of cancer, including glioblastoma, suggesting that STAT3 is a potential therapeutic target for cancer therapy. We recently identified ODZ10117 as a small molecule inhibitor of STAT3 and suggested that it may have an effective therapeutic utility for the STAT3-targeted cancer therapy. Here, we demonstrated the therapeutic efficacy of ODZ10117 in glioblastoma by targeting STAT3. ODZ10117 inhibited migration and invasion and induced apoptotic cell death by targeting STAT3 in glioblastoma cells and patient-derived primary glioblastoma cells. In addition, ODZ10117 suppressed stem cell properties in glioma stem cells (GSCs). Finally, the administration of ODZ10117 showed significant therapeutic efficacy in mouse xenograft models of GSCs and glioblastoma cells. Collectively, ODZ10117 is a promising therapeutic candidate for glioblastoma by targeting STAT3.

Indexed as

AnimalsCell Line, TumorDisease Models, AnimalGlioblastomaHumansMiceSTAT3 Transcription FactorSurvival AnalysisXenograft Model Antitumor AssaysStat3 protein, mouseSTAT3 Transcription Factorglioblastomaglioma stem cell (GSC)ODZ10117STAT3targeted therapy

Identifiers

PMID32183406
PMCPMC7140655
OpenAlexW3012257591

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.