Evidence map›Paper›PMID 36926607›Full record

ArticleJournal of ginseng research2023

Ginsenoside Rb2 suppresses cellular senescence of human dermal fibroblasts by inducing autophagy.

Kyeong Eun Yang, Soo-Bin Nam, Minsu Jang, Junsoo Park, Ga-Eun Lee, Yong-Yeon Cho, Byeong-Churl Jang, Cheol-Jung Lee, Jong-Soon Choi

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  5. Journal of ginseng research · 2025
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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

9 authors at 5 institutions in 1 country.

Kyeong Eun YangBio-Chemical Analysis Group, Center for Research Equipment, Korea Basic Science Institute, Daejeon, Republic of Korea.
Soo-Bin NamResearch Center for Materials Analysis, Korea Basic Science Institute, Daejeon, Republic of Korea.
Minsu JangDivision of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.
Junsoo ParkDivision of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.
Ga-Eun LeeBRL & BK21-4th Team, College of Pharmacy, The Catholic University of Korea, Gyeonggi, Republic of Korea.
Yong-Yeon ChoBRL & BK21-4th Team, College of Pharmacy, The Catholic University of Korea, Gyeonggi, Republic of Korea.
Byeong-Churl JangDepartment of Molecular Medicine, College of Medicine, Keimyung University, Daegu, Republic of Korea.
Cheol-Jung LeeResearch Center for Materials Analysis, Korea Basic Science Institute, Daejeon, Republic of Korea.
Jong-Soon ChoiResearch Center for Materials Analysis, Korea Basic Science Institute, Daejeon, Republic of Korea.
Catholic University of Korea · KRChungnam National University · KRKorea Basic Science Institute · KRYonsei University · KRKeimyung University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ginsenoside Rb2, a major active component of Methods: We performed a senescence-associated β-galactosidase staining assay to confirm cellular senescence in human dermal fibroblasts (HDFs). The regulatory effects of Rb2 on autophagy were evaluated by analyzing the expression of autophagy marker proteins, such as microtubule-associated protein 1A/1B-light chain (LC) 3 and p62, using immunoblotting. Autophagosome and autolysosome formation was monitored using transmission electron microscopy. Autophagic flux was analyzed using tandem-labeled GFP-RFP-LC3, and lysosomal function was assessed with Lysotracker. We performed RNA sequencing to identify potential target genes related to HDF rejuvenation mediated by Rb2. To verify the functions of the target genes, we silenced them using shRNAs. Results: Rb2 decreased β-galactosidase activity and altered the expression of cell cycle regulatory proteins in senescent HDFs. Rb2 markedly induced the conversion of LC3-Ⅰ to LC3-Ⅱ and LC3 puncta. Moreover, Rb2 increased lysosomal function and red puncta in tandem-labeled GFP-RFP-LC3, which indicate that Rb2 promoted autophagic flux. RNA sequencing data showed that the expression of DNA damage-regulated autophagy modulator 2 (DRAM2) was induced by Rb2. In autophagy signaling, Rb2 activated the AMPK-ULK1 pathway and inactivated mTOR. Conclusion: Rb2 reverses cellular senescence by activating autophagy via the AMPK-mTOR pathway and induction of DRAM2, suggesting that Rb2 might have potential value as an antiaging agent.

Indexed as

AutophagyDRAM2Rb2Senescence

Identifiers

PMID36926607
PMCPMC10014224
OpenAlexW4308924092

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.