Evidence map›Paper›PMID 34671019›Full record

ArticleCell death & disease2021

RANBP10 promotes glioblastoma progression by regulating the FBXW7/c-Myc pathway.

Jianbing Hou, Yudong Liu, Pan Huang, Yutao Wang, Dakun Pei, Ruoyue Tan, Yundong Zhang, Hongjuan Cui

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. RANBP9 and RANBP10 cooperate in regulating non-small cell lung cancer proliferation.Journal of experimental & clinical cancer research : CR · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. FBXW7 in breast cancer: mechanism of action and therapeutic potential.Journal of experimental & clinical cancer research : CR · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

8 authors at 3 institutions in 1 country.

Jianbing Hou *State Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Yudong Liu *State Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Pan HuangState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Yutao WangDepartment of Neurology, the Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Dakun PeiState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Ruoyue TanState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China.
Yundong ZhangDepartment of Neurology, the Third Affiliated Hospital of Chongqing Medical University, Chongqing, China. zhangghx68@sina.com.ORCID 0000-0002-3284-0851
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Southwest University, 400716, Chongqing, China. hongjuan.cui@gmail.com.ORCID 0000-0003-1178-1570
Southwest University · CNArmy Medical University · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RAN binding protein 10 (RANBP10), a ubiquitously expressed and evolutionarily conserved protein, as a RAN-GTP exchange factor (GEF) to regulate several factors involved in cellular progression. Previous studies showed that RANBP10 was overexpressed in prostate cancer cells and was responsible for androgen receptor (AR) activation. However, the biological function of RANBP10 in glioblastoma (GBM) has not been studied. Here, we found that RANBP10 was overexpressed in GBM, and high RANBP10 expression was closely linked to poor survival of patients with GBM. Downregulation of RANBP10 significantly inhibited cell proliferation, migration, invasion, and tumor growth of GBM cells. In addition, we revealed that RANBP10 could suppress the promoter activity of FBXW7, and thereby increase the protein stability of c-Myc in GBM cells. Silencing of FBXW7 in RANBP10-knockdown GBM cells could partly negate the effects induced by RANBP10 downregulation. Taken together, our findings established that RANBP10 significantly promoted GBM progression by control of the FBXW7-c-Myc axis, and suggest that RANBP10 may be a potential target in GBM.

Indexed as

Disease ProgressionGene Expression Regulation, NeoplasticSignal TransductionAdultAnimalsCell CycleCell Line, TumorCell MovementCell ProliferationF-Box-WD Repeat-Containing Protein 7FemaleGene SilencingGlioblastomaGuanine Nucleotide Exchange FactorsHumansMaleF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanGuanine Nucleotide Exchange FactorsMicrotubule-Associated ProteinsProto-Oncogene Proteins c-mycRANBP10 protein, human

Identifiers

PMID34671019
PMCPMC8528885
OpenAlexW3205300895

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.