Evidence map›Paper›PMID 24846311›Full record

ArticlePloS one2014

Luteolin modulates 6-hydroxydopamine-induced transcriptional changes of stress response pathways in PC12 cells.

Ling-Wei Hu, Jui-Hung Yen, Yi-Ting Shen, Kuan-Yi Wu, Ming-Jiuan Wu

Open 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. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Therapeutic Expedition of Luteolin against Brain-related Disorders: An Updated Review.Combinatorial chemistry & high throughput screening · 2025
    Review
  7. Review
  8. Luteolin for neurodegenerative diseases: a review.Pharmacological reports : PR · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Suppressing Cdk5 Activity by Luteolin Inhibits MPPMolecules (Basel, Switzerland) · 2021
    Article
  19. Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Ling-Wei HuDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Jui-Hung YenDepartment of Molecular Biology and Human Genetics, Tzu Chi University, Hualien, Taiwan.
Yi-Ting ShenDepartment of Pharmacy, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Kuan-Yi WuDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Ming-Jiuan WuDepartment of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.
Chia Nan University of Pharmacy and Science · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The neurotoxin 6-hydroxydopamine (6-OHDA), which causes transcriptional changes associated with oxidative and proteotoxic stress, has been widely used to generate an experimental model of Parkinson's disease. The food-derived compound luteolin has multi-target actions including antioxidant, anti-inflammatory and neurotrophic activities. The aim of this study is to investigate how luteolin affects 6-OHDA-mediated stress response pathways. The results showed that when PC12 cells were pre-treated with luteolin (20 µM) 30 min prior to 6-OHDA (100 µM) exposure, 6-OHDA-induced ROS overproduction, cytotoxicity, caspase-3 activation, and mRNA expression of BIM, TRB3 and GADD34 were significantly attenuated. Moreover, 6-OHDA-mediated cell cycle arrest and transcription of p53 target genes, p21, GADD45α and PUMA, were reduced by luteolin. Luteolin also significantly down-regulated 6-OHDA-mediated unfolded protein response (UPR), leading to decreases in phospho-eIF2α, ATF4, GRP78 and CHOP. In addition, luteolin attenuated 6-OHDA-induced Nrf2-mediated HO-1 and GCLC. Taken together, these results suggest that diminishing intracellular ROS formation and down-regulation of p53, UPR and Nrf2-ARE pathways may be involved in the neuroprotective effect of luteolin.

Indexed as

Activating Transcription Factor 4Activating Transcription Factor 6AnimalsApoptosisCell Cycle CheckpointsCell SurvivalEndoplasmic Reticulum Chaperone BiPGene Expression RegulationHeat-Shock ProteinsLuteolinNF-E2-Related Factor 2OxidopaminePC12 CellsRatsReactive Oxygen SpeciesRNA, MessengerActivating Transcription Factor 4Activating Transcription Factor 6Endoplasmic Reticulum Chaperone BiPGRP78 protein, ratHeat-Shock ProteinsHSPA5 protein, humanLuteolinNF-E2-Related Factor 2OxidopamineReactive Oxygen SpeciesRNA, MessengerTranscription Factor CHOPTumor Suppressor Protein p53

Identifiers

PMID24846311
PMCPMC4028259
OpenAlexW1970102981

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.