Evidence map›Paper›PMID 33199761›Full record

ArticleScientific reports2020

Platycodin D enhances LDLR expression and LDL uptake via down-regulation of IDOL mRNA in hepatic cells.

Yu-Jeong Choi, Sol Ji Lee, Hyo In Kim, Hee Jung Lee, So Jung Kang, Tai Young Kim, Chunhoo Cheon, Seong-Gyu Ko

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  8. Article
  9. Review
  10. Review
  11. Review
  12. Triterpenoids fromACS omega · 2023
    Article
  13. Review
  14. Review
  15. Article
  16. Frontiers in pharmacology · 2022
    Article
  17. Article
  18. Bioactive Triterpenes ofInternational journal of molecular sciences · 2021
    Article
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 at 2 institutions in 1 country.

Yu-Jeong ChoiDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Sol Ji LeeDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Hyo In KimDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Hee Jung LeeDepartment Global Public Health and Korean Medicine Management, College of Korean Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
So Jung KangDepartment of Clinical Koeran Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Tai Young KimCenter for Cognition and Sociality, Institute for Basic Science, Daejeon, 34126, Republic of Korea. taik@ibs.re.kr.
Chunhoo CheonDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, 1 Hoegi, Seoul, 130-701, Korea.
Seong-Gyu KoDepartment of Preventive Medicine, College of Korean Medicine, Kyung Hee University, 1 Hoegi, Seoul, 130-701, Korea. epiko@khu.ac.kr.
Kyung Hee University · KRInstitute for Basic Science · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The root of Platycodon grandiflorum (PG) has long been used as a traditional herbal medicine in Asian country. Platycondin D (PD), triterpenoid saponin that is a main constituent of PG, exhibits various biological activities such as anti-inflammatory, anti-oxidant, anti-diabetic, and anti-cancer effects. A previous study showed that PD had cholesterol-lowering effects in mice that develop hypercholesterolemia, but the underlying molecular mechanisms have not been elucidated during the last decade. Here, we demonstrated that both PG and PD markedly increased levels of cell surface low-density lipoprotein receptor (LDLR) by down-regulation of the E3 ubiquitin ligase named inducible degrader of the LDLR (IDOL) mRNA, leading to the enhanced uptake of LDL-derived cholesterol (LDL-C) in hepatic cells. Furthermore, cycloheximide chase analysis and in vivo ubiquitination assay revealed that PD increased the half-life of LDLR protein by reducing IDOL-mediated LDLR ubiquitination. Finally, we demonstrated that treatment of HepG2 cells with simvastatin in combination with PG and PD had synergistic effects on the improvement of LDLR expression and LDL-C uptake. Together, these results provide the first molecular evidence for anti-hypercholesterolemic activity of PD and suggest that PD alone or together with statin could be a potential therapeutic option in the treatment of atherosclerotic cardiovascular disease.

Indexed as

Cell LineCholesterol, LDLCycloheximideDrug SynergismGene Expression RegulationHalf-LifeHepatocytesHep G2 CellsHumansPlant RootsPlatycodonReceptors, LDLSaponinsSimvastatinTriterpenesUbiquitinationCholesterol, LDLCycloheximideLDLR protein, humanMYLIP protein, humanplatycodin DReceptors, LDLSaponinsSimvastatinTriterpenesUbiquitin-Protein Ligases

Identifiers

PMID33199761
PMCPMC7670405
OpenAlexW3104675007

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.