Evidence map›Paper›PMID 26636541›Full record

ArticleOncotarget2016

Ginsenoside Rg3 inhibits epithelial-mesenchymal transition (EMT) and invasion of lung cancer by down-regulating FUT4.

Lili Tian, Dachuan Shen, Xiaodong Li, Xiu Shan, Xiaoqi Wang, Qiu Yan, Jiwei Liu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% 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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Molecular mechanisms and therapeutic targets in lung cancer-nerve crosstalk.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  3. Article
  4. Article
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  7. Non-small cell lung cancer map and analysis: exploring interconnected oncogenic signal integrators.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  8. Review
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  11. Article
  12. Review
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12 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

7 authors at 3 institutions in 2 countries.

Lili TianDepartment of Oncology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Dachuan ShenInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, Liaoning Province, China.
Xiaodong LiInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, Liaoning Province, China.
Xiu ShanDepartment of Oncology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Xiaoqi WangDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America.
Qiu YanDepartment of Biochemistry and Molecular Biology, Liaoning Provincial Core Lab of Glycobiology and Glycoengineering, Dalian Medical University, Dalian, Liaoning Province, China.
Jiwei LiuDepartment of Oncology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Dalian Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CNNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial-mesenchymal transition (EMT) is an important factor in lung cancer metastasis, and targeting EMT is a potential therapeutic strategy. Fucosyltransferase IV (FUT4) and its synthetic cancer sugar antigen Lewis Y (LeY) was abnormally elevated in many cancers. In this study, a traditional Chinese medicine ginsenoside Rg3 was used to investigate whether its inhibition to EMT and invasion of lung cancer is by the glycobiology mechanism. We found that Rg3 treatment (25, 50, 100 μg/ml) inhibited cell migration and invasion by wound-healing and transwell assays. Rg3 could significantly alter EMT marker proteins with increased E-cadherin, but decreased Snail, N-cadherin and Vimentin expression. Rg3 also down-regulated FUT4 gene and protein expression in lung cancer cells by qPCR, Western blot and immunofluorescence. After FUT4 down-regulated with shFUT4, EMT was obviously inhibited. Furthermore, the activation of EGFR through decreased LeY biosynthesis was inhibited, which blocked the downstream MAPK and NF-κB signal pathways. In addition, Rg3 reduced tumor volume and weight in xenograft mouse model, and significantly decreased tumor metastasis nodules in lung tissues by tail vein injection. In conclusion, Rg3 inhibits EMT and invasion of lung cancer by down-regulating FUT4 mediated EGFR inactivation and blocking MAPK and NF-κB signal pathways. Rg3 may be a potentially effective agent for the treatment of lung cancer.

Indexed as

A549 CellsAnimalsBlotting, WesternCadherinsCell MovementDown-RegulationEpithelial-Mesenchymal TransitionFucosyltransferasesGene Expression Regulation, NeoplasticGinsenosidesHumansImmunohistochemistryLewis X AntigenLung NeoplasmsMaleMice, Inbred BALB CCadherinsFucosyltransferasesFUT4 protein, humanginsenoside Rg3GinsenosidesLewis X AntigenVimentinEGFREMTFUT4lung cancerRg3

Identifiers

PMID26636541
PMCPMC4811485
OpenAlexW2191249569

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.