Evidence map›Paper›PMID 42911431›Full record

ArticleBiogerontology2026

Resveratroloside alleviates senescence-associated phenotypes in vitro through the coordinated regulation of mitochondrial function and chromatin structure.

Jee Hee Yoon, Ye Hyang Kim, Duyeol Kim, Eun Young Jeong, So Hun Lee, Ha Yeon Kim, Ji Ho Park, Moon Kyoung So, Yoo Jin Lee, Minseon Kim and 5 more

Abstract read
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In one paragraph

Article in Biogerontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Jee Hee Yoon *Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Ye Hyang Kim *Hyundai Bioland Co., Ltd., 22, Osongsaengmyeong 2-Ro, Osong-Eup, Heungdeok-Gu, Cheongju-Si, 28162, Republic of Korea.
Duyeol Kim *Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Eun Young Jeong *Hyundai Bioland Co., Ltd., 22, Osongsaengmyeong 2-Ro, Osong-Eup, Heungdeok-Gu, Cheongju-Si, 28162, Republic of Korea.
So Hun LeeHyundai Bioland Co., Ltd., 22, Osongsaengmyeong 2-Ro, Osong-Eup, Heungdeok-Gu, Cheongju-Si, 28162, Republic of Korea.
Ha Yeon KimHyundai Bioland Co., Ltd., 22, Osongsaengmyeong 2-Ro, Osong-Eup, Heungdeok-Gu, Cheongju-Si, 28162, Republic of Korea.
Ji Ho ParkDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Moon Kyoung SoDivision 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.
Minseon KimDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Jihyun SongDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Sehui LimDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea.
Youngjoo ByunCollege of Pharmacy, Korea University, Sejong, 30019, Republic of Korea.
Song Seok ShinHyundai Bioland Co., Ltd., 22, Osongsaengmyeong 2-Ro, Osong-Eup, Heungdeok-Gu, Cheongju-Si, 28162, Republic of Korea.
Joon Tae ParkDivision of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, Republic of Korea. joontae.park@inu.ac.kr.

Funding

Incheon National University 2024-0077
6 · The paper itself

Abstract

Cellular senescence is characterized by coordinated disruptions in mitochondrial function and epigenetic regulation, with perturbation of the mitochondria-chromatin axis emerging as a central hallmark of this process. Resveratrol (RSV) has been extensively investigated as a modulator of this axis; however, its clinical utility is constrained by dose-dependent cytotoxicity. Here, we evaluated the safety profile and anti-aging potential of resveratrol glucoside (R-glc), a glucosylated derivative of RSV. R-glc exhibited markedly reduced cytotoxicity compared to RSV and effectively attenuated multiple senescence-associated phenotypes at low concentrations. Mechanistically, R-glc enhanced mitochondrial function, as evidenced by increased oxidative phosphorylation and reduced glycolytic dependence. At the epigenetic level, R-glc upregulated the NAD

Indexed as

Cellular SenescenceChromatinGlucosidesMitochondriaResveratrolStilbenesEpigenesis, GeneticHumansPhenotypeChromatinGlucosidesResveratrolStilbenesEpigenetic regulationMitochondrial functionResveratrolR-glc

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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.