Evidence map›Paper›PMID 33643049›Full record

ArticleFrontiers in pharmacology2021

Combination of Ginsenosides Rb2 and Rg3 Promotes Angiogenic Phenotype of Human Endothelial Cells via PI3K/Akt and MAPK/ERK Pathways.

Ran Joo Choi, Siti Zuraidah Mohamad Zobir, Ben Alexander-Dann, Nitin Sharma, Marcella K L Ma, Brian Y H Lam, Giles S H Yeo, Weidong Zhang, Tai-Ping Fan, Andreas Bender

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Nutrients · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Frontiers in pharmacology · 2023
    Article
  10. Article
  11. 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

10 authors at 4 institutions in 2 countries.

Ran Joo ChoiDepartment of Chemistry, Center for Molecular Science Informatics, University of Cambridge, Cambridge, United Kingdom.
Siti Zuraidah Mohamad ZobirDepartment of Chemistry, Center for Molecular Science Informatics, University of Cambridge, Cambridge, United Kingdom.
Ben Alexander-DannDepartment of Chemistry, Center for Molecular Science Informatics, University of Cambridge, Cambridge, United Kingdom.
Nitin SharmaDepartment of Chemistry, Center for Molecular Science Informatics, University of Cambridge, Cambridge, United Kingdom.
Marcella K L MaMedical Research Council (MRC) Metabolic Diseases Unit, University of Cambridge Metabolic Research Laboratories, Wellcome-MRC Institute of Metabolic Science, Genomics and Transcriptomics Core, Addenbrooke's Hospital, Cambridge, United Kingdom.
Brian Y H LamMedical Research Council (MRC) Metabolic Diseases Unit, University of Cambridge Metabolic Research Laboratories, Wellcome-MRC Institute of Metabolic Science, Genomics and Transcriptomics Core, Addenbrooke's Hospital, Cambridge, United Kingdom.
Giles S H YeoMedical Research Council (MRC) Metabolic Diseases Unit, University of Cambridge Metabolic Research Laboratories, Wellcome-MRC Institute of Metabolic Science, Genomics and Transcriptomics Core, Addenbrooke's Hospital, Cambridge, United Kingdom.
Weidong ZhangDepartment of Pharmacy, Second Military Medical University, Shanghai, China.
Tai-Ping FanDepartment of Pharmacology, University of Cambridge, Cambridge, United Kingdom.
Andreas BenderDepartment of Chemistry, Center for Molecular Science Informatics, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBAddenbrooke's Hospital · GBMedical Research Council · GBSecond Military Medical University · CN

Funding

Medical Research Council MC_UU_00014/5Wellcome Trust
6 · The paper itself

Abstract

Shexiang Baoxin Pill (SBP) is an oral formulation of Chinese materia medica for the treatment of angina pectoris. It displays pleiotropic roles in protecting the cardiovascular system. However, the mode of action of SBP in promoting angiogenesis, and in particular the synergy between its constituents is currently not fully understood. The combination of ginsenosides Rb2 and Rg3 were studied in human umbilical vein endothelial cells (HUVECs) for their proangiogenic effects. To understand the mode of action of the combination in more mechanistic detail, RNA-Seq analysis was conducted, and differentially expressed genes (DEGs), pathway analysis and Weighted Gene Correlation Network Analysis (WGCNA) were applied to further identify important genes that a play pivotal role in the combination treatment. The effects of pathway-specific inhibitors were observed to provide further support for the hypothesized mode of action of the combination. Ginsenosides Rb2 and Rg3 synergistically promoted HUVEC proliferation and tube formation under defined culture conditions. Also, the combination of Rb2/Rg3 rescued cells from homocysteine-induced damage. mRNA expression of

Indexed as

angiogenesisginsenoside Rb2ginsenoside Rg3RNA-seqshexiang baoxin pillsynergistic combinationtube formationweighted gene correlation network analysis

Identifiers

PMID33643049
PMCPMC7902932
OpenAlexW3126600322

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.