Evidence map›Paper›PMID 25078449›Full record

ArticleMolecules and cells2014

Systemic approaches identify a garlic-derived chemical, Z-ajoene, as a glioblastoma multiforme cancer stem cell-specific targeting agent.

Yuchae Jung, Heejoo Park, Hui-Yuan Zhao, Raok Jeon, Jae-Ha Ryu, Woo-Young Kim

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.2field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Short Total Synthesis of Ajoene.Angewandte Chemie (International ed. in English) · 2018
    Article
  14. Article
  15. Article
  16. Therapeutic Role of Functional Components in Alliums for Preventive Chronic Disease in Human Being.Evidence-based complementary and alternative medicine : eCAM · 2017
    Review
  17. Review
  18. ROS-mediated activation of JNK/p38 contributes partially to the pro-apoptotic effect of ajoene on cells of lung adenocarcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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

6 authors at 1 institution in 1 country.

Yuchae JungResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Heejoo ParkResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Hui-Yuan ZhaoResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Raok JeonResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Jae-Ha RyuResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Woo-Young KimResearch Center for Cell Fate Control (RCCFC) and College of Pharmacy, Sookmyung Women's University, Seoul 140-742, Korea.
Sookmyung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is one of the most common brain malignancies and has a very poor prognosis. Recent evidence suggests that the presence of cancer stem cells (CSC) in GBM and the rare CSC subpopulation that is resistant to chemotherapy may be responsible for the treatment failure and unfavorable prognosis of GBM. A garlic-derived compound, Z-ajoene, has shown a range of biological activities, including anti-proliferative effects on several cancers. Here, we demonstrated for the first time that Z-ajoene specifically inhibits the growth of the GBM CSC population. CSC sphere-forming inhibition was achieved at a concentration that did not exhibit a cytotoxic effect in regular cell culture conditions. The specificity of this inhibitory effect on the CSC population was confirmed by detecting CSC cell surface marker CD133 expression and biochemical marker ALDH activity. In addition, stem cell-related mRNA profiling and real-time PCR revealed the differential expression of CSC-specific genes, including Notch, Wnt, and Hedgehog, upon treatment with Z-ajoene. A proteomic approach, i.e., reverse-phase protein array (RPPA) and Western blot analysis, showed decreased SMAD4, p-AKT, 14.3.3 and FOXO3A expression. The protein interaction map (http://string-db.org/) of the identified molecules suggested that the AKT, ERK/p38 and TGFβ signaling pathways are key mediators of Z-ajoene's action, which affects the transcriptional network that includes FOXO3A. These biological and bioinformatic analyses collectively demonstrate that Z-ajoene is a potential candidate for the treatment of GBM by specifically targeting GBM CSCs. We also show how this systemic approach strengthens the identification of new therapeutic agents that target CSCs.

Indexed as

GarlicDisulfidesDrug Resistance, NeoplasmForkhead Box Protein O3Forkhead Transcription FactorsGene Expression Regulation, DevelopmentalGlioblastomaGrowth InhibitorsHedgehog ProteinsHumansMAP Kinase Signaling SystemMolecular Targeted TherapyNeoplastic Stem CellsOncogene Protein v-aktReceptors, NotchSmad4 ProteinajoeneDisulfidesForkhead Box Protein O3Forkhead Transcription FactorsFOXO3 protein, humanGrowth InhibitorsHedgehog ProteinsOncogene Protein v-aktReceptors, NotchSmad4 ProteinSulfoxidesTransforming Growth Factor beta1Wnt ProteinsajoeneCSCgarlicGBM

Identifiers

PMID25078449
PMCPMC4132307
OpenAlexW2007102767

What OpenQuestion holds

Textmetadata
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.