Evidence map›Paper›PMID 38791186›Full record

ArticleInternational journal of molecular sciences2024

Quercetin Induces Mitochondrial Apoptosis and Downregulates Ganglioside GD3 Expression in Melanoma Cells.

Sang Young Seo, Won Seok Ju, Kyongtae Kim, Juhwan Kim, Jin Ok Yu, Jae-Sung Ryu, Ji-Su Kim, Hyun-A Lee, Deog-Bon Koo, Young-Kug Choo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Application of Modulators of CaInternational journal of molecular sciences · 2025
    Article
  7. Plants (Basel, Switzerland) · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

10 authors.

Sang Young SeoDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.ORCID 0000-0002-7823-9295
Won Seok JuDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.ORCID 0000-0002-3359-8315
Kyongtae KimDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.
Juhwan KimDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.
Jin Ok YuDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.
Jae-Sung RyuDivision of Biodrug Evaluation, New Drug Development Center, Osong Medical Innovation Foundation (K-Bio Health), Cheongju 28160, Chungbuk, Republic of Korea.
Ji-Su KimPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Jeongeup 56216, Jeonbuk, Republic of Korea.
Hyun-A LeeCenter for Animal Resources Development, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.
Deog-Bon KooDepartment of Biotechnology, College of Engineering, Daegu University, Gyeongsan 38453, Gyeongbuk, Republic of Korea.ORCID 0000-0001-7825-9598
Young-Kug ChooDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Jeonbuk, Republic of Korea.

Funding

National Research Foundation of Korea (NRF) grant funded by the Master of Science in Infor-mation Technology (MSIT) 2023R1A2C1003066
6 · The paper itself

Abstract

Malignant melanoma represents a form of skin cancer characterized by a bleak prognosis and heightened resistance to traditional therapies. Quercetin has demonstrated notable anti-carcinogenic, anti-inflammatory, anti-oxidant, and pharmacological effects across various cancer types. However, the intricate relationship between quercetin's anti-cancer properties and ganglioside expression in melanoma remains incompletely understood. In this study, quercetin manifests specific anti-proliferative, anti-migratory, and cell-cycle arrest effects, inducing mitochondrial dysfunction and apoptosis in two melanoma cancer cell lines. This positions quercetin as a promising candidate for treating malignant melanoma. Moreover, our investigation indicates that quercetin significantly reduces the expression levels of ganglioside GD3 and its synthetic enzyme. Notably, this reduction is achieved through the inhibition of the FAK/paxillin/Akt signaling pathway, which plays a crucial role in cancer development. Taken together, our findings suggest that quercetin may be a potent anti-cancer drug candidate for the treatment of malignant melanoma.

Indexed as

ApoptosisGangliosidesMelanomaMitochondriaQuercetinCell Line, TumorCell MovementCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHumansProto-Oncogene Proteins c-aktSignal TransductionSkin Neoplasmsganglioside, GD3GangliosidesProto-Oncogene Proteins c-aktQuercetinapoptosiscell-cycle arrestgangliosideknockdownmalignant melanomaquercetin

Identifiers

PMID38791186
PMCPMC11121576

What OpenQuestion holds

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Registered trials

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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.