Evidence map›Paper›PMID 24558306›Full record

ArticleJournal of ginseng research2014

Stereospecific anticancer effects of ginsenoside Rg3 epimers isolated from heat-processed American ginseng on human gastric cancer cell.

Eun-Hwa Park, Young-Joo Kim, Noriko Yamabe, Soon-Hye Park, Ho-Kyong Kim, Hyuk-Jai Jang, Ji Hoon Kim, Gab Jin Cheon, Jungyeob Ham, Ki Sung Kang

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 139 citations in OpenAlex.

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  12. Ginsenoside 20(S)-Rg3 reducesJournal of ginseng research · 2024
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  19. The Effect of Shenyi Capsule on Non-Small-Cell Lung Cancer Combined with Chemotherapy from theEvidence-based complementary and alternative medicine : eCAM · 2021
    Review
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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

10 authors at 3 institutions in 1 country.

Eun-Hwa ParkDepartment of Surgery, University of Ulsan College of Medicine, Gangneung, Korea.
Young-Joo KimNatural Medicine Center, Korea Institute of Science and Technology, Gangneung, Korea.
Noriko YamabeNatural Medicine Center, Korea Institute of Science and Technology, Gangneung, Korea.
Soon-Hye ParkRichwood Pharmaceutical Co., Ltd., Seoul, Korea.
Ho-Kyong KimRichwood Pharmaceutical Co., Ltd., Seoul, Korea.
Hyuk-Jai JangDepartment of Surgery, University of Ulsan College of Medicine, Gangneung, Korea.
Ji Hoon KimDepartment of Surgery, University of Ulsan College of Medicine, Gangneung, Korea.
Gab Jin CheonDepartment of Internal Medicine, University of Ulsan College of Medicine, Gangneung, Korea.
Jungyeob HamNatural Medicine Center, Korea Institute of Science and Technology, Gangneung, Korea.
Ki Sung KangNatural Medicine Center, Korea Institute of Science and Technology, Gangneung, Korea.
Korea Institute of Science and Technology · KRUniversity of Ulsan · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResearch has been conducted with regard to the development of methods for improving the pharmaceutical effect of ginseng by conversion of ginsenosides, which are the major active components of ginseng, via high temperature or high-pressure processing.

methodsThe present study sought to investigate the anticancer effect of heat-processed American ginseng (HAG) in human gastric cancer AGS cells with a focus on assessing the role of apoptosis as an important mechanistic element in its anticancer actions. RESULTS AND

conclusionHAG significantly reduced the cancer cell proliferation, and the contents of ginsenosides Rb1 and Re were markedly decreased, whereas the peaks of less-polar ginsenosides [20(S,R)-Rg3, Rk1, and Rg5] were newly detected. Based on the activity-guided fractionation of HAG, ginsenoside 20(S)-Rg3 played a key role in inducing apoptosis in human gastric cancer AGS cells, and it was generated mainly from ginsenoside Rb1. Ginsenoside 20(S)-Rg3 induced apoptosis through activation of caspase-3, caspase-8, and caspase-9, as well as regulation of Bcl-2 and Bax expression. Taken together, these findings suggest that heat-processing serves as an increase in the antitumor activity of American ginseng in AGS cells, and ginsenoside 20(S)-Rg3, the active component produced by heat-processing, induces the activation of caspase-3, caspase-8, and caspase-9, which contributes to the apoptotic cell death.

Indexed as

American ginsengginsenoside20(S)-Rg3heat processingPanax quinquefolius

Identifiers

PMID24558306
PMCPMC3915326
OpenAlexW2084981437

What OpenQuestion holds

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LicenceCC BY-NC
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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.