Evidence map›Paper›PMID 28208648›Full record

ArticleInternational journal of molecular sciences2017

RETRACTED: n-Butylidenephthalide Regulated Tumor Stem Cell Genes EZH2/AXL and Reduced Its Migration and Invasion in Glioblastoma.

Ssu-Yin Yen, Hong-Meng Chuang, Mao-Hsuan Huang, Shinn-Zong Lin, Tzyy-Wen Chiou, Horng-Jyh Harn

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. RETRACTED: Yen et al.International journal of molecular sciences · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. International journal of molecular sciences · 2021
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. The Molecular Mechanisms of Plant-Derived Compounds Targeting Brain Cancer.International journal of molecular sciences · 2018
    Review
  18. Article
  19. Cell transplantation
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Ssu-Yin YenDepartment of Life Science and Graduate Institute of Biotechnology, National Dong Hwa University, Hualien 974, Taiwan. momoyin911@gmail.com.
Hong-Meng ChuangBuddhist Tzu Chi Bioinnovation Center, Tzu Chi Foundation, Hualien 970, Taiwan. kavin273@gmail.com.
Mao-Hsuan HuangBuddhist Tzu Chi Bioinnovation Center, Tzu Chi Foundation, Hualien 970, Taiwan. spleo0825@gmail.com.
Shinn-Zong LinBuddhist Tzu Chi Bioinnovation Center, Tzu Chi Foundation, Hualien 970, Taiwan. shinnzong@yahoo.com.tw.
Tzyy-Wen ChiouDepartment of Life Science and Graduate Institute of Biotechnology, National Dong Hwa University, Hualien 974, Taiwan. twchiou@mail.ndhu.edu.tw.
Horng-Jyh HarnBuddhist Tzu Chi Bioinnovation Center, Tzu Chi Foundation, Hualien 970, Taiwan. arthewduke@gmail.com.
Tzu Chi Foundation · TWNational Chung Hsing University · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is one of the most common and aggressive types of brain tumor. Due to its highly recurrent rate and poor prognosis, the overall survival time with this type of tumor is only 20-21 months. Recent knowledge suggests that its recurrence is in part due to the presence of cancer stem cells (CSCs), which display radioresistant, chemoresistant, self-renewal and tumorigenic potential. Enhancers of Zeste 2 (EZH2) and AXL receptor tyrosine kinase (AXL) are both highly expressed in GBM. Additionally, they are an essential regulator involved in CSCs maintenance, migration, invasion, epithelial-to-mesenchymal transition (EMT), stemness, metastasis and patient survival. In this study, we used a small molecule, n-butylidenephthalide (BP), to assess the anti-GBM stem-like cells potential, and then tried to find out the associated genes involved with regulation in migration and invasion. We demonstrated that BP reduced the expression of AXL and stemness related genes in a dose-dependent manner. The migratory and invasive capabilities of GBM stem-like cells could be reduced by AXL/EZH2. Finally, in the overexpression of AXL, EZH2 and Sox2 by transfection in GBM stem-like cells, we found that AXL/EZH2/TGF-ꞵ1, but not Sox2, might be a key regulator in tumor invasion, migration and EMT. These results might help in the development of a new anticancer compound and can be a target for treating GBM.

Indexed as

Axl Receptor Tyrosine KinaseBiomarkersBrain NeoplasmsCell CycleCell Line, TumorCell MovementCell ProliferationCell Self RenewalEnhancer of Zeste Homolog 2 ProteinEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGlioblastomaHumansModels, BiologicalNeoplastic Stem CellsPhenotypeAXL protein, humanAxl Receptor Tyrosine KinaseBiomarkersbutylidenephthalideEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanPhthalic AnhydridesProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAXL receptor tyrosine kinasecancer stem cells (CSCs)enhancer of Zeste 2 (EZH2)glioblastoma (GBM)n-butylidenephthalide (BP)

Identifiers

PMID28208648
PMCPMC5343907
OpenAlexW2588647775

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.