Evidence map›Paper›PMID 26617790›Full record

ArticleInternational journal of clinical and experimental pathology2015

GM130 regulates epithelial-to-mesenchymal transition and invasion of gastric cancer cells via snail.

Jianquan Zhao, Chun Yang, Shujun Guo, Yonggang Wu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  10. The role of the Golgi apparatus in disease (Review).International journal of molecular medicine · 2021
    Review
  11. The Role of GM130 in Nervous System Diseases.Frontiers in neurology · 2021
    Review
  12. Review
  13. Adaptation of the Golgi Apparatus in Cancer Cell Invasion and Metastasis.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
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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 2 institutions in 1 country.

Jianquan ZhaoDepartment of Cardiology, Bayannaoer City Hospital Inner Mongolia, China.
Chun YangDepartment of Medical Cosmetology Bayannaoer City Hospital Inner Mongolia, China.
Shujun GuoDepartment of Cardiology, Bayannaoer City Hospital Inner Mongolia, China.
Yonggang WuDepartment of Orthopedics, Bayannaoer City Hospital Inner Mongolia, China.
Inner Mongolia People's Hospital · CNInner Mongolia Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is one of the most common causes of digestive tract tumor. Despite of recent advances in surgical techniques and development of adjuvant therapy, the underlying mechanisms of gastric cancer remain poorly understood and relevant insight into novel treatment strategies using gene target remains incomplete. Recently, several studies report that epithelial to mesenchymal transition (EMT) is a crucial process for the invasion and metastasis of epithelial tumors; however, the molecular mechanisms underlying this transition are unknown. As a cis-Golgi matrix protein, GM130 plays an important role in cell cycle progression and transport of protein in the secretory pathway. In this study, we found that GM130 expression has a positive correlation with the pathological differentiation and tumor node metastasis (TNM) stage of gastric cancer. High GM130 expression levels also predict shorter overall survival of gastric cancer patients. RNA interference-mediated knockdown of GM130 expression increased epithelial marker (E-cadherin) and decreased mesenchymal marker (N-cadherin and vimentin) expression in gastric cancer cells, suppressing cell invasion, and tumor formation. Furthermore, we found that GM130 upregulated expression of the key EMT regulator Snail (SNAI1), which mediated EMT activation and cell invasion by GM130. Taken together, our study indicates GM130 may be a promising therapeutic biomarker for gastric cancer.

Indexed as

Cell MovementEpithelial-Mesenchymal TransitionAntigens, CDAutoantigensBinding SitesBiomarkers, TumorCadherinsCell DifferentiationCell Line, TumorGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMembrane ProteinsNeoplasm InvasivenessNeoplasm StagingPromoter Regions, GeneticAntigens, CDAutoantigensBiomarkers, TumorCadherinsCDH1 protein, humanCDH2 protein, humanGolgin subfamily A member 2Membrane ProteinsSNAI1 protein, humanSnail Family Transcription FactorsTranscription FactorsVimentinEMTgastric cancerGM130invasionmigration

Identifiers

PMID26617790
PMCPMC4637605
OpenAlexW2418260534

What OpenQuestion holds

Textmetadata
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.