Evidence map›Paper›PMID 27051448›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2016

Effect of Amino Acids on the Generation of Ginsenoside Rg3 Epimers by Heat Processing and the Anticancer Activities of Epimers in A2780 Human Ovarian Cancer Cells.

Jun Yeon Park, Pilju Choi, Dahae Lee, Taejung Kim, Eun Bee Jung, Buyng-Su Hwang, Ki Sung Kang, Jungyeob Ham

Abstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

7 citing papers in PubMed.

  1. Review
  2. Ginsenoside 20(S)-Rg3 reducesJournal of ginseng research · 2024
    Article
  3. Review
  4. Article
  5. Stereoisomers of Saponins inFrontiers in pharmacology · 2018
    Review
  6. Article
  7. Saponins from Chinese Medicines as Anticancer Agents.Molecules (Basel, Switzerland) · 2016
    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

8 authors.

Jun Yeon ParkCollege of Korean Medicine, Gachon University, Seongnam 461-701, Republic of Korea.
Pilju ChoiKIST Gangneung Institute of Natural Products, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.
Dahae LeeCollege of Korean Medicine, Gachon University, Seongnam 461-701, Republic of Korea.
Taejung KimKIST Gangneung Institute of Natural Products, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.
Eun Bee JungCollege of Korean Medicine, Gachon University, Seongnam 461-701, Republic of Korea.
Buyng-Su HwangKIST Gangneung Institute of Natural Products, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.
Ki Sung KangCollege of Korean Medicine, Gachon University, Seongnam 461-701, Republic of Korea.
Jungyeob HamKIST Gangneung Institute of Natural Products, Korea Institute of Science and Technology, Gangneung 210-340, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ginsenosides are the active components of Panax ginseng. Many research studies indicate that these deglycosylated, less-polar ginsenosides have better bioactivity than the major ginsenosides. In the present study, we sought to verify the enhanced anticancer effect of P. ginseng extract after undergoing the Maillard reaction as well as elucidate the underlying mechanism of action. The effects of 9 amino acids were tested; among them, the content of 20(S)-Rg3 in the ginseng extract increased to more than 30, 20, and 20% when processed with valine, arginine, and alanine, respectively, compared with that after normal heat processing. The ginseng extract that was heat-processed with arginine exhibited the most potent inhibitory effect on A2780 ovarian cancer cell proliferation. Therefore, the generation of 20(S)-Rg3 was suggested to be involved in this effect. Moreover, the inhibitory effect of 20(S)-Rg3 on A2780 cell proliferation was significantly stronger than that of 20(R)-Rg3. Protein expression levels of cleaved caspase-3, caspase-8, caspase-9, and PARP in the A2780 ovarian cancer cells markedly increased, whereas the expression of BID decreased after 20(S)-Rg3 treatment. Therefore, we confirmed that the anticancer effects of the products of ginseng that was heat-processed with arginine are mediated mainly via the generation of the less-polar ginsenoside 20(S)-Rg3.

Identifiers

PMID27051448
PMCPMC4804038

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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.