Evidence map›Paper›PMID 31296839›Full record

ArticleCell death & disease2019

KHDRBS3 regulates the permeability of blood-tumor barrier via cDENND4C/miR-577 axis.

Peiqi Wu, Yang Gao, Shuyuan Shen, Yixue Xue, Xiaobai Liu, Xuelei Ruan, Lianqi Shao, Yunhui Liu, Ping Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Peiqi WuDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Yang GaoDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Shuyuan ShenDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Yixue XueDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Xuelei RuanDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Lianqi ShaoDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Yunhui LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Ping WangDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China. pingwang8000@163.com.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The existence of blood-tumor barrier (BTB) severely restricts the efficient delivery of antitumor drugs to cranial glioma tissues. Various strategies have been explored to increase BTB permeability. RNA-binding proteins and circular RNAs have recently emerged as potential regulators of endothelial cells functions. In this study, RNA-binding protein KH RNA-binding domain containing, signal transduction associated 3 (KHDRBS3) and circular RNA DENND4C (cDENND4C) were enriched in GECs. KHDRBS3 bound to cDENND4C and increased its stability. The knockdown of cDENND4C increased the permeability of BTB via downregulating the expressions of tight junction-related proteins. The miR-577 was lower expressed in GECs. The overexpressed miR-577 increased the permeability of BTB by reducing the tight junction-related protein expressions, and vice versa. Furthermore, cDENND4C acted as a molecular sponge of miR-577, which bound to miR-577 and inhibited its negative regulation of target genes ZO-1, occludin and claudin-1 to regulate BTB permeability. Single or combined treatment of KHDRBS3, cDENND4C, and miR-577 effectively promoted antitumor drug doxorubicin (DOX) across BTB to induce apoptosis of glioma cells. Collectively, the present study indicated that KHDRBS3 could regulate BTB permeability through the cDENND4C/miR-577 axis, which enhanced doxorubicin delivery across BTB. These findings may provide a novel strategy for chemotherapy of brain tumors.

Indexed as

Antibiotics, AntineoplasticApoptosisBlood-Brain BarrierBrain NeoplasmsCell Line, TumorClaudin-1DoxorubicinEndothelial CellsGliomaHumansMicroRNAsOccludinPermeabilityRNA-Binding ProteinsRNA, CircularTight JunctionsAntibiotics, AntineoplasticClaudin-1CLDN1 protein, humanDoxorubicinKHDRBS3 protein, humanMicroRNAsMIRN577 microRNA, humanOccludinRNA-Binding ProteinsRNA, CircularZonula Occludens-1 Protein

Identifiers

PMID31296839
PMCPMC6624200
OpenAlexW2959520494

What Socratic 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 Socratic graph.