Evidence map›Paper›PMID 37252280›Full record

ArticleJournal of ginseng research2023

Systemic and molecular analysis dissect the red ginseng induction of apoptosis and autophagy in HCC as mediated with AMPK.

Young Woo Kim, Seon Been Bak, Won-Yung Lee, Su Jin Bae, Eun Hye Lee, Ju-Hye Yang, Kwang Youn Kim, Chang Hyun Song, Sang Chan Kim, Un-Jung Yun and 1 more

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

11 authors at 5 institutions in 1 country.

Young Woo KimSchool of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Seon Been BakSchool of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Won-Yung LeeSchool of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Su Jin BaeSchool of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Eun Hye LeeCollege of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Ju-Hye YangKorean Medicine (KM) Application Center, Korea Institute of Oriental Medicine, Daegu, Republic of Korea.
Kwang Youn KimKorean Medicine (KM) Application Center, Korea Institute of Oriental Medicine, Daegu, Republic of Korea.
Chang Hyun SongMRC center, College of Korean Medicine, Daegu Haany University, Gyeongsan, Republic of Korea.
Sang Chan KimMRC center, College of Korean Medicine, Daegu Haany University, Gyeongsan, Republic of Korea.
Un-Jung YunSchool of Korean Medicine, Dongguk University, Gyeongju, Republic of Korea.
Kwang Il ParkDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National University, Jinju, Republic of Korea.
Dongguk University · KRDaegu Haany University · KRKorea Institute of Oriental Medicine · KRGyeongsang National University · KRKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatocellular carcinoma (HCC) has a high incidence and is one of the highest mortality cancers when advanced stage is proceeded. However, Anti-cancer drugs available for treatment are limited and new anti-cancer drugs and new ways to treat them are minimal. We examined that the effects and possibility of Red Ginseng (RG, Panax ginseng Meyer) as new anti-cancer drug on HCC by combining network pharmacology and molecular biology. Materials and Methods: Network pharmacological analysis was employed to investigate the systems-level mechanism of RG focusing on HCC. Cytotoxicity of RG was determined by MTT analysis, which were also stained by annexin V/PI staining for apoptosis and acridine orange for autophagy. For the analyze mechanism of RG, we extracted protein and subjected to immunoblotting for apoptosis or autophagy related proteins. Results: We constructed compound-target network of RG and identified potential pathways related to HCC. RG inhibited growth of HCC through acceleration of cytotoxicity and reduction of wound healing ability of HCC. RG also increased apoptosis and autophagy through AMPK induction. In addition, its ingredients, 20S-PPD (protopanaxadiol) and 20S-PPT (protopanaxatriol), also induced AMPK mediated apoptosis and autophagy. Conclusion: RG effectively inhibited growth of HCC cells inducing apoptosis and autophagy via ATG/AMPK in HCC cells. Overall, our study suggests possibility as new anti-cancer drug on HCC by proof for the mechanism of the anti-cancer action of RG.

Indexed as

AMPKApoptosisHCCNetwork pharmacologyRed ginseng

Identifiers

PMID37252280
PMCPMC10214298
OpenAlexW4321602475

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.