Evidence map›Paper›PMID 24520214›Full record

ArticleInternational journal of biological sciences2014

Inhibition of lymphangiogenesis of endothelial progenitor cells with VEGFR-3 siRNA delivered with PEI-alginate nanoparticles.

Ting Li, Guo-dong Wang, Yu-zhen Tan, Hai-jie Wang

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2014. 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
2.2field-weighted citation impact, top 11% 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, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. CD34 positive cells as endothelial progenitor cells in biology and medicine.Frontiers in cell and developmental biology · 2023
    Review
  5. Review
  6. Biomaterials for Modulating Lymphatic Function in Immunoengineering.ACS pharmacology & translational science · 2019
    Review
  7. Article
  8. Article
  9. Review
  10. Vascular stem/progenitor cells: functions and signaling pathways.Cellular and molecular life sciences : CMLS · 2018
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Jin Fu Kang Oral Liquid Inhibits Lymphatic Endothelial Cells Formation and Migration.Evidence-based complementary and alternative medicine : eCAM · 2016
    Article
  18. 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

4 authors at 1 institution in 1 country.

Ting LiDepartment of Anatomy, Histology and Embryology, Shanghai Medical School of Fudan University, Shanghai 200032, China.
Guo-dong WangDepartment of Anatomy, Histology and Embryology, Shanghai Medical School of Fudan University, Shanghai 200032, China.
Yu-zhen TanDepartment of Anatomy, Histology and Embryology, Shanghai Medical School of Fudan University, Shanghai 200032, China.
Hai-jie WangDepartment of Anatomy, Histology and Embryology, Shanghai Medical School of Fudan University, Shanghai 200032, China.
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphangiogenesis is implicated in lymphatic metastasis of tumor cells. Recently, growing evidences show that endothelial progenitor cells (EPCs) are involved in lymphangiogenesis. This study has investigated effects of VEGF-C/VEGFR-3 (vascular endothelial growth factor receptor-3) signaling pathway on EPC differentiation and effectiveness of inhibiting lymphatic formation of EPCs with VEGFR-3 siRNA delivered in PEI (polyethylenimine)-alginate nanoparticles. CD34(+)VEGFR-3(+) EPCs were sorted from mononuclear cells of human cord blood. Under induction with VEGF-C, the cells differentiated toward lymphatic endothelial cells. The nanoparticles were formulated with 25 kDa branched PEI and alginate. The size and surface charge of PEI-alginate nanoparticles loading VEGFR-3 siRNA (N/P = 16) are 139.1 nm and 7.56 mV respectively. VEGFR-3 siRNA specifically inhibited expression of VEGFR-3 mRNA in the cells. After treatment with PEI-alginate/siRNA nanocomplexes, EPCs could not differentiate into lymphatic endothelial cells, and proliferation, migration and lymphatic formation of EPC-derived cells were suppressed significantly. These results demonstrate that VEGFR-3 signaling plays an important role in differentiation of CD34(+)VEGFR-3(+) EPCs. VEGFR-3 siRNA delivered with PEI-alginate nanoparticles can effectively inhibit differentiation and lymphangiogenesis of EPCs. Inhibiting VEGFR-3 signaling with siRNA/nanocomplexes would be a potential therapy for suppression of tumor lymphangiogenesis and lymphatic metastasis.

Indexed as

NanoparticlesRNA InterferenceAlginatesAntigens, CD34Cell DifferentiationCell MovementEndothelial CellsFetal BloodGlucuronic AcidHexuronic AcidsHumansLymphangiogenesisMicroscopy, Electron, ScanningPolyethyleneimineRNA, Small InterferingStem CellsAlginatesAntigens, CD34Glucuronic AcidHexuronic AcidsPolyethyleneimineRNA, Small InterferingVascular Endothelial Growth Factor Receptor-3alginate.endothelial progenitor cellsnanoparticlespolyethyleneimineVEGFR-3

Identifiers

PMID24520214
PMCPMC3920171
OpenAlexW2160335182

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.