Evidence map›Paper›PMID 22286231›Full record

ArticleMolecules and cells2012

Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein-coupled lysophosphatidic acid receptors with high affinity.

Sung Hee Hwang, Tae-Joon Shin, Sun-Hye Choi, Hee-Jung Cho, Byung-Hwan Lee, Mi Kyung Pyo, Jun-Ho Lee, Jiyeon Kang, Hyeon-Joong Kim, Chan-Woo Park and 2 more

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In one paragraph

Article in Molecules and cells, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

80 citing papers in PubMed, 109 citations in OpenAlex.

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  12. Gintonin-EnrichedFoods (Basel, Switzerland) · 2025
    Article
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20 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 1 country.

Sung Hee HwangGinsentology Research Laboratory and Department of Physiology, and Bio/Molecular Informatics Center, College of Veterinary Medicine, Konkuk University, Seoul 143-701, Korea.
Tae-Joon Shin
Sun-Hye Choi
Hee-Jung Cho
Byung-Hwan Lee
Mi Kyung Pyo
Jun-Ho Lee
Jiyeon Kang
Hyeon-Joong Kim
Chan-Woo Park
Ho-Chul Shin
Seung-Yeol Nah
Konkuk University · KRKonkuk University Medical Center · KRInternational Ginseng & Herb Research Institute · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we isolated a subset of glycolipoproteins from Panax ginseng, that we designated gintonin, and demonstrated that it induced [Ca2+]i transients in cells via G protein-coupled receptor (GPCR) signaling pathway(s). However, active components responsible for Ca2+ mobilization and the corresponding receptor(s) were unknown. Active component(s) for [Ca2+]i transients of gintonin were analyzed by liquid chromatography-electrospray ionization-tandem mass spectrometry and ion-mobility mass spectrometry, respectively. The corresponding receptor(s)were investigated through gene expression assays. We found that gintonin contains LPA C18:2 and other LPAs. Proteomic analysis showed that ginseng major latex-like protein and ribonuclease-like storage proteins are protein components of gintonin. Gintonin induced [Ca2+]i transients in B103 rat neuroblastoma cells transfected with human LPA receptors with high affinity in order of LPA2 >LPA5 > LPA1 > LPA3 > LPA4. The LPA1/LPA3 receptor antagonist Ki16425 blocked gintonin action in cells expressing LPA1 or LPA3. Mutations of binding sites in the LPA3 receptor attenuated gintonin action. Gintonin acted via pertussis toxin (PTX)-sensitive and -insensitive G protein-phospholipase C (PLC)-inositol 1,4,5-trisphosphate (IP3)-Ca2+ pathways. However, gintonin had no effects on other receptors examined. In human umbilical vein endothelial cells (HUVECs) gintonin stimulated cell proliferation and migration. Gintonin stimulated ERK1/2 phosphorylation. PTX blocked gintonin-mediated migration and ERK1/2 phosphorylation. In PC12 cells gintonin induced morphological changes, which were blocked by Rho kinase inhibitorY-27632. Gintonin contains GPCR ligand LPAs in complexes with ginseng proteins and could be useful in the development of drugs targeting LPA receptors.

Indexed as

AnimalsCalcium SignalingCell Line, TumorCell MovementCell ProliferationEndothelium, VascularGene Expression ProfilingGlycoproteinsGTP-Binding ProteinsHumansIsoxazolesLysophospholipidsMolecular Targeted TherapyMutagenesis, Site-DirectedMutationPanax3-(4-(4-((1-(2-chlorophenyl)ethoxy)carbonyl amino)-3-methyl-5-isoxazolyl) benzylsulfanyl) propanoic acidgintoninGlycoproteinsGTP-Binding ProteinsIsoxazolesLysophospholipidsPertussis ToxinPlant ExtractsPlant ProteinsPropionatesReceptors, Lysophosphatidic Acid

Identifiers

PMID22286231
PMCPMC3887723
OpenAlexW2055129301

What OpenQuestion holds

Textmetadata
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.