Evidence map›Paper›PMID 39275030›Full record

ArticleMolecules (Basel, Switzerland)2024

Identification of Cellular Isoschaftoside-Mediated Anti-Senescence Mechanism in

Yun Haeng Lee, Byeong Hyeon So, Kyeong Seon Lee, Myeong Uk Kuk, Ji Ho Park, Jee Hee Yoon, Yoo Jin Lee, Du Yeol Kim, Min Seon Kim, Hyung Wook Kwon and 3 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. ε-Viniferin Rejuvenates Senescence viaPharmaceuticals (Basel, Switzerland) · 2025
    Article
  8. 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

13 authors.

Yun Haeng LeeDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Byeong Hyeon SoDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Kyeong Seon LeeCollege of Pharmacy, Korea University, Sejong 30019, Republic of Korea.
Myeong Uk KukDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Ji Ho ParkDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Jee Hee YoonDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Yoo Jin LeeDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Du Yeol KimDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Min Seon KimDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.
Hyung Wook KwonDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.ORCID 0000-0001-9340-7974
Youngjoo ByunCollege of Pharmacy, Korea University, Sejong 30019, Republic of Korea.ORCID 0000-0002-0297-7734
Ki Yong LeeCollege of Pharmacy, Korea University, Sejong 30019, Republic of Korea.ORCID 0000-0002-6191-4485
Joon Tae ParkDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Republic of Korea.ORCID 0000-0003-2396-9108

Funding

Ministry of Health & Welfare HP23C0024National Research Foundation of Korea 2019R1A6A1A03031807National Research Foundation of Korea 2020R1A6A1A0304195411National Research Foundation of Korea NRF2021R1A2C1093814
6 · The paper itself

Abstract

As cellular senescence, reactive oxygen species (ROS) accumulate excessively, causing cellular damage. Flavonoids derived from natural products are known for their antioxidant effects and their ability to delay cellular senescence. Previous studies have attempted to mitigate cellular senescence using flavonoids from natural sources. However, the detailed mechanisms and regulatory targets of some flavonoids exhibiting antioxidant effects have not been fully elucidated. Therefore, we screened a library of flavonoids for antioxidant properties. Isoschaftoside, a glycosidic flavonoid, significantly reduced ROS levels in senescent cells. It was found that mitochondrial function was restored, and dependence on glycolysis was reduced in senescent cells treated with isoschaftoside. Additionally, we identified that isoschaftoside suppresses ROS by reducing the expression of

Indexed as

AntioxidantsCellular SenescenceRAC2 GTP-Binding Proteinrac GTP-Binding ProteinsReactive Oxygen SpeciesCell LineFlavonoidsGlycosidesHumansMitochondriaAntioxidantsFlavonoidsGlycosidesRAC2 GTP-Binding Proteinrac GTP-Binding ProteinsReactive Oxygen Speciesflavonoidisoschaftosidereactive oxygen species (ROS)senescence amelioration

Identifiers

PMID39275030
PMCPMC11397025

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.