Evidence map›Paper›PMID 33557814›Full record

ArticleBMC complementary medicine and therapies2021

Panax notoginseng saponins promote endothelial progenitor cell angiogenesis via the Wnt/β-catenin pathway.

Peiqi Zhu, Weidong Jiang, Shixi He, Tao Zhang, Fengchun Liao, Di Liu, Xiaoning An, Xuanping Huang, Nuo Zhou

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 33% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Effective Components ofACS omega · 2025
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Drug design, development and therapy · 2024
    Article
  12. Article
  13. Article
  14. Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  15. Notoginseng Triterpenes Inhibited Autophagy in Random FlapsFrontiers in bioengineering and biotechnology · 2021
    Article
  16. 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

9 authors at 2 institutions in 1 country.

Peiqi Zhu *Guangxi Medical University, Nanning, 530021, People's Republic of China.
Weidong Jiang *Guangxi Medical University, Nanning, 530021, People's Republic of China.
Shixi HeGuangxi Medical University, Nanning, 530021, People's Republic of China.
Tao ZhangGuangxi Medical University, Nanning, 530021, People's Republic of China.
Fengchun LiaoGuangxi Medical University, Nanning, 530021, People's Republic of China.
Di LiuGuangxi Medical University, Nanning, 530021, People's Republic of China.
Xiaoning AnGuangxi Medical University, Nanning, 530021, People's Republic of China.
Xuanping HuangGuangxi Medical University, Nanning, 530021, People's Republic of China. hxp120@126.com.
Nuo ZhouGuangxi Medical University, Nanning, 530021, People's Republic of China. gxzhounuo@sina.cn.ORCID http://orcid.org/0000-0002-3645-2151
Guangxi University · CNGuangxi Medical University · CN

Funding

National Natural Science Foundation of China No. 81670970National Natural Science Foundation of China No. 81870748
6 · The paper itself

Abstract

backgroundDistraction osteogenesis (DO) is an effective treatment in craniomaxillofacial surgery. However, the issue of sufficient blood supply at the regeneration tissue has limited its wide application. Panax notoginseng saponins (PNS) is a Traditional Chinese Medicine that is commonly used to treat a range of angiogenic diseases. However, the mechanisms whereby PNS alters angiogenesis in endothelial progenitor cells (EPCs) have yet to be clarified.

methodsEPCs were identified by immunofluorescence, confirmed by their uptake of fluorescently labeled Dil-ac-LDL and FITC-UEA-1. EPCs were treated with different concentrations of PNS, and the effects of PNS on cell proliferation were measured on the optimal concentration of PNS determined. The effects of PNS on angiogenesis and migration, angiogenic cytokines mRNA expression and the proteins of the Wnt pathway were investigated. Then knocked down β-catenin in EPCs and treated with the optimum concentrational PNS, their angiogenic potential was evaluated in tube formation and migration assays. In addition, the expression of cytokines associated with angiogenesis and Wnt/β-catenin was then assessed via WB and RT-qPCR.

resultsWe were able to determine the optimal concentration of PNS in the promotion of cell proliferation, tube formation, and migration to be 6.25 mg/L. PNS treatment increased the mRNA levels of VEGF, bFGF, VE-Cadherin, WNT3a, LRP5, β-catenin, and TCF4. After knocked down β-catenin expression, we found that PNS could sufficient to partially reverse the suppression of EPC angiogenesis.

conclusionsOverall, 6.25 mg/L PNS can promote EPC angiogenesis via Wnt/β-catenin signaling pathway activation.

Indexed as

AnimalsCell MovementCell ProliferationCells, CulturedDogsEndothelial Progenitor CellsMaleNeovascularization, PhysiologicPanax notoginsengSaponinsWnt Signaling PathwaySaponinsAngiogenesisEndothelial progenitor cellsPanax notoginseng saponinsWnt/β-catenin signaling

Identifiers

PMID33557814
PMCPMC7869233
OpenAlexW3126164967

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.