Evidence map›Paper›PMID 39901566›Full record

ArticleACS nano2025

Graphene Quantum Dots Attenuate TDP-43 Proteinopathy in Amyotrophic Lateral Sclerosis.

Na Young Park, Yunseok Heo, Ji Won Yang, Je Min Yoo, Hye Ji Jang, Ju Hee Jo, Su Jeong Park, Yuxi Lin, Joonhyeok Choi, Hyeonjin Jeon and 14 more

Abstract read
In one paragraph

Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. TSC2 is a stress granule suppressor.bioRxiv : the preprint server for biology · 2026
    Article
  4. Graphene Quantum Dots Mitigate Oxidative Stress in Bacteria.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. 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

24 authors.

Na Young ParkDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Yunseok HeoBiopharmaceutical Research Center, Korea Basic Science Institute, Cheongju 28119, Korea.ORCID 0000-0002-2233-4306
Ji Won YangDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Je Min YooChaperone Ventures, LLC., Los Angeles, California 90006, United States.ORCID 0000-0003-3074-859X
Hye Ji JangDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Ju Hee JoDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Su Jeong ParkDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Yuxi LinBiopharmaceutical Research Center, Korea Basic Science Institute, Cheongju 28119, Korea.
Joonhyeok ChoiBiopharmaceutical Research Center, Korea Basic Science Institute, Cheongju 28119, Korea.
Hyeonjin JeonDementia Research Group, Korea Brain Research Institute, Daegu 41062, Korea.
Sun Joo ChaDementia Research Group, Korea Brain Research Institute, Daegu 41062, Korea.
Gaeun BaeDepartment of Chemistry and Advanced Institute of Convergence Technology, Seoul National University, Seoul 08826, Korea.
Donghoon KimDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.
Juhee KimMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California 90089, United States.
Wade ZenoMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California 90089, United States.ORCID 0000-0002-2341-8923
Jong Bo ParkGraphene Square Chemical Inc., Pohang 37673, Korea.
Noriyoshi IsozumiDepartment of Future Basic Medicine, Nara Medical University, Nara 634-8521, Japan.
Tomohide SaioInstitute of Advanced Medical Sciences, Tokushima University, Tokushima 770-0855, Japan.ORCID 0000-0003-3639-7399
Seung Hyun KimDepartment of Neurology, College of Medicine, Hanyang University, Seoul 04763, Korea.
Hojae LeeBiomanufacturing Center, Cedars-Sinai Medical Center, West Hollywood, California 90048, United States.
Byung Hee HongDepartment of Chemistry and Advanced Institute of Convergence Technology, Seoul National University, Seoul 08826, Korea.ORCID 0000-0001-8355-8875
Minyeop NahmDementia Research Group, Korea Brain Research Institute, Daegu 41062, Korea.
Young-Ho LeeBiopharmaceutical Research Center, Korea Basic Science Institute, Cheongju 28119, Korea.ORCID 0000-0002-8441-5814
Young Bin HongDepartment of Translational Biomedical Sciences, Graduate School of Dong-A University, Busan 49201, Korea.ORCID 0000-0002-4333-3847

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant phase separation- and stress granule (SG)-mediated cytosolic aggregation of TDP-43 in motor neurons is the hallmark of amyotrophic lateral sclerosis (ALS). In this study, we found that graphene quantum dots (GQDs) potentially modulate TDP-43 aggregation during SG dynamics and phase separation. The intrinsically disordered region in the C-terminus of TDP-43 exhibited amyloid fibril formation; however, GQDs inhibited the formation of amyloid fibrils through direct intermolecular interactions with TDP-43. These effects were accompanied by attenuation of the ALS phenotype in animal models. Additionally, GQDs delayed the onset and survival of TDP-43 transgenic mouse models by enhancing motor neuron survival, reducing glial activation, and reducing the cytosolic aggregation of TDP-43 in motor neurons. In this research, we demonstrated the efficacy of GQDs on the SG-mediated aggregation of TDP-43 and the binding property of GQDs with TDP-43. Additionally, we demonstrated the clinical feasibility of GQDs using several animal models and other types of ALS caused by FUS and C9orf72. Therefore, GQDs could offer a new therapeutic approach for proteinopathy-associated ALS.

Indexed as

Amyotrophic Lateral SclerosisDNA-Binding ProteinsGraphiteQuantum DotsTDP-43 ProteinopathiesAnimalsDisease Models, AnimalHumansMiceMice, TransgenicMotor NeuronsDNA-Binding ProteinsGraphiteTARDBP protein, humangraphene quantum dotsliquid−liquid phase separationstress granulesTDP-43

Identifiers

PMID39901566
PMCPMC11912580

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.