Evidence map›Paper›PMID 32432570›Full record

ArticleAging2020

Qigesan inhibits esophageal cancer cell invasion and migration by inhibiting Gas6/Axl-induced epithelial-mesenchymal transition.

Lingyu Kong, Xin Lu, Xuanyu Chen, Yunyan Wu, Yushuang Zhang, Huijuan Shi, Jing Li

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. AXL in cancer: a modulator of drug resistance and therapeutic target.Journal of experimental & clinical cancer research : CR · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. AXL, an Important Host Factor for DENV and ZIKV Replication.Frontiers in cellular and infection microbiology · 2021
    Review
  9. 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

7 authors at 3 institutions in 1 country.

Lingyu KongCollege of Integrated Chinese and Western Medicine, Hebei Medical University, Shijiazhuang 050017, Hebei, China.
Xin LuDepartment of Clinical Laboratory, Tangshan Maternal and Children Hospital, Tangshan 063000, Hebei, China.
Xuanyu ChenCollege of Integrated Chinese and Western Medicine, Hebei Medical University, Shijiazhuang 050017, Hebei, China.
Yunyan WuResearch Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China.
Yushuang ZhangDepartment of Traditional Chinese Medicine, Tumor Hospital of Hebei Province, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China.
Huijuan ShiDepartment of Traditional Chinese Medicine, Tumor Hospital of Hebei Province, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China.
Jing LiCollege of Integrated Chinese and Western Medicine, Hebei Medical University, Shijiazhuang 050017, Hebei, China.
Hebei Medical University · CNFourth Hospital of Hebei Medical University · CNTangshan People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Qigesan (QGS) has been used to effectively treat esophageal cancer (EC) for decades in China, but the mechanism by which it suppresses EC metastasis remains unknown. In this study, we examined the effects of QGS on EC cell mobility. Using immunohistochemistry and immunofluorescence, expression of Gas6 and Axl, which promote tumor cell migration and invasion, was examined in carcinoma tissues and adjacent normal tissues from EC patients. Levels of Gas6, Axl, and the Gas6/Axl complex were also examined in ECA109 and TE13 EC cells treated with QGS. In addition, immunofluorescent staining and quantitative protein analysis were used to examine E-cadherin, N-cadherin, and Snail levels in ECA109 and TE13 EC cells after QSG administration, and cell mobility was assessed. The results demonstrated that levels of Gas6 and Axl expression are higher in EC tissues than in adjacent normal tissues. Moreover, QGS decreased Gas6/Axl levels, increased E-cadherin expression, decreased Snail and N-cadherin expression, and inhibited epithelial-mesenchymal transition (EMT) in EC cells. QGS thus suppresses EMT in EC by inhibiting Gas6/Axl binding.

Indexed as

Antineoplastic AgentsAxl Receptor Tyrosine KinaseCell Line, TumorCell MovementDrugs, Chinese HerbalEpithelial-Mesenchymal TransitionEsophageal NeoplasmsGrowth Arrest-Specific Protein 6HumansIntercellular Signaling Peptides and ProteinsNeoplasm InvasivenessProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAntineoplastic AgentsAXL protein, humanAxl Receptor Tyrosine KinaseDrugs, Chinese HerbalGrowth Arrest-Specific Protein 6Intercellular Signaling Peptides and ProteinsProto-Oncogene ProteinsqigesanReceptor Protein-Tyrosine Kinasescancer metastasisepithelial-mesenchymal transitionESCCGas6/AxlTCM formulas

Identifiers

PMID32432570
PMCPMC7288918
OpenAlexW3026265561

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.