Evidence map›Paper›PMID 32713259›Full record

ArticleRNA biology2020

IGF2BP2 stabilized FBXL19-AS1 regulates the blood-tumour barrier permeability by negatively regulating ZNF765 by STAU1-mediated mRNA decay.

Xiaobai Liu, Peiqi Wu, Rui Su, Yixue Xue, Chunqing Yang, Di Wang, Xuelei Ruan, Jian Zheng, Yang Yang, Zhen Li and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. The Critical Role of RNA mCellular and molecular neurobiology · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. mCell death discovery · 2021
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

11 authors at 1 institution in 1 country.

Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.ORCID 0000-0001-7690-0847
Peiqi WuDepartment of Neurobiology, School of Life Sciences, China Medical University , Shenyang, China.
Rui SuDepartment of Neurobiology, School of Life Sciences, China Medical University , Shenyang, China.
Yixue XueDepartment of Neurobiology, School of Life Sciences, China Medical University , Shenyang, China.
Chunqing YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
Di WangDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
Xuelei RuanDepartment of Neurobiology, School of Life Sciences, China Medical University , Shenyang, China.
Jian ZhengDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
Yang YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
Zhen LiDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
Yunhui LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University , Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blood-tumour barrier (BTB) has been known to significantly attenuate the efficacy of chemotherapy for glioma. In this report, we identified that insulin-like grown factor 2 mRNA-binding protein 2 (IGF2BP2) was over-expressed in glioma microvessel and glioma endothelial cells (GECs). Knockdown of IGF2BP2 decreased the expression of lncRNA FBXL19-AS1 and tight junction-related proteins, thereby promoting BTB permeability. FBXL19-AS1 was over-expressed and more enriched in the cytoplasm of GECs. In addition, FBXL19-AS1 could bind to 3'-UTR of ZNF765 mRNA and down-regulate ZNF765 mRNA expression through STAU1-mediated mRNA decay (SMD). The low expression of ZNF765 was discovered in GECs and verified to increase BTB permeability by inhibiting the promoter activities of tight junction-related proteins. Meanwhile, ZNF765 also inhibited the transcriptional activity of IGF2BP2, thereby forming a feedback loop in regulating the BTB permeability. Single or combined application of silenced IGF2BP2 and FBXL19-AS1 improved the delivery and antitumor efficiency of doxorubicin (DOX). In general, our study revealed the regulation mechanism of IGF2BP2/FBXL19-AS1/ZNF765 axis on BTB permeability, which may provide valuable insight into treatment strategy for glioma.

Indexed as

Gene Expression Regulation, NeoplasticTumor MicroenvironmentCell Line, TumorCytoskeletal ProteinsDNA-Binding ProteinsEndothelial CellsF-Box ProteinsGene Knockdown TechniquesHumansNonsense Mediated mRNA DecayPermeabilityProtein BindingRNA-Binding ProteinsRNA, Long NoncodingRNA StabilityTranscriptomeCytoskeletal ProteinsDNA-Binding ProteinsF-Box ProteinsFBXL19 protein, humanIGF2BP2 protein, humanRNA-Binding ProteinsRNA, Long NoncodingSTAU1 protein, humanblood-tumour barrierFBXL19-AS1IGF2BP2stau1-mediated decay

Identifiers

PMID32713259
PMCPMC7714532
OpenAlexW3043841083

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.