Evidence map›Paper›PMID 27904777›Full record

ArticleAmerican journal of cancer research2016

G3BP1 contributes to tumor metastasis via upregulation of Slug expression in hepatocellular carcinoma.

Ning Dou, Jingde Chen, Shijun Yu, Yong Gao, Yandong Li

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  5. Article
  6. Role(s) of G3BPs in Human Pathogenesis.The Journal of pharmacology and experimental therapeutics · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. G3BP1 inhibits Cul3Nature communications · 2021
    Article
  12. Article
  13. The Emerging Role of Stress Granules in Hepatocellular Carcinoma.International journal of molecular sciences · 2021
    Review
  14. Heat shock proteins-driven stress granule dynamics: yet another avenue for cell survival.Apoptosis : an international journal on programmed cell death · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. The Integral Role of RNA in Stress Granule Formation and Function.Frontiers in cell and developmental biology · 2021
    Review
  20. 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

5 authors at 1 institution in 1 country.

Ning DouDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, China.
Jingde ChenDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, China.
Shijun YuDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, China.
Yong GaoDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, China.
Yandong LiDepartment of Oncology, Shanghai East Hospital, Tongji University School of MedicineShanghai 200120, China; Research Center for Translational Medicine, Shanghai East Hospital, Tongji University School of MedicineShanghai 200120, China.
Shanghai East Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RasGAP SH3-domain-Binding Protein 1 (G3BP1) has been implicated in cell growth, migration, and metastasis of some cancers, yet its function in hepatocellular carcinoma (HCC) remains to be explored. In the present study, we reported that G3BP1 was upregulated in HCC tissues compared with adjacent non-cancerous liver tissues both in mRNA and protein levels, and its high expression was significantly correlated with poor prognosis of HCC patients. Functional analyses demonstrated that forced expression of G3BP1 in HCC cells promoted cell migration, and silenced expression of G3BP1 by RNA interference caused opposite effects. Moreover, G3BP1 knockdown attenuated the distant metastasis capacity of HCC cells through tail vein injection approach in nude mice model. At molecular mechanism, we found G3BP1 knockdown decreased Slug expression, and increased the expression of the epithelial cell marker E-cadherin. Overexpression of Slug could restore the phenotype of G3BP1 silencing induced cell migration inhibition. Together, our data establish G3BP1 as an oncogenic factor involved in the metastasis of HCC and suggest that G3BP1 might serve as a novel predictor for patients' outcome.

Indexed as

G3BP1hepatocellular carcinomaSlugtumor metastasis

Identifiers

PMID27904777
PMCPMC5126279
OpenAlexW2582569671

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.