Evidence map›Paper›PMID 38639925›Full record

ArticleMolecular cancer research : MCR2024

NSCLC Extracellular Vesicles Containing miR-374a-5p Promote Leptomeningeal Metastasis by Influencing Blood‒Brain Barrier Permeability.

Jie Jin, Yumeng Cui, Huicong Niu, Yanli Lin, Xiaojie Wu, Xuejiao Qi, Kaixuan Bai, Yu Zhang, Youliang Wang, Hui Bu

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

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  8. Extracellular vesicles for delivery of functional telomerase.Cell communication and signaling : CCS · 2025
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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

10 authors at 2 institutions in 1 country.

Jie Jin *The Second Hospital of Hebei Medical University, Shijiazhuang, PR China.ORCID 0009-0005-1334-4683
Yumeng Cui *Beijing Institute of Biotechnology, Beijing, PR China.ORCID 0009-0001-0287-5623
Huicong NiuDepartment of Neurology, Minhang Hospital, Fudan University, Shanghai, PR China.ORCID 0000-0001-9112-8883
Yanli LinBeijing Institute of Biotechnology, Beijing, PR China.ORCID 0000-0002-7711-9355
Xiaojie WuBeijing Institute of Biotechnology, Beijing, PR China.ORCID 0000-0001-7307-5503
Xuejiao QiThe Second Hospital of Hebei Medical University, Shijiazhuang, PR China.ORCID 0000-0003-2012-9568
Kaixuan BaiThe Second Hospital of Hebei Medical University, Shijiazhuang, PR China.ORCID 0000-0002-3259-0020
Yu ZhangThe Second Hospital of Hebei Medical University, Shijiazhuang, PR China.ORCID 0000-0001-5680-4452
Youliang WangBeijing Institute of Biotechnology, Beijing, PR China.ORCID 0000-0003-1319-0344
Hui BuThe Second Hospital of Hebei Medical University, Shijiazhuang, PR China.ORCID 0009-0007-8716-3265
Hebei Medical University · CNFudan University · CN

Funding

National Key Research and Development Program of China (NKPs) 2019YFA0903800Natural Science Foundation of Hebei Province () H2020206126
6 · The paper itself

Abstract

Leptomeningeal metastasis (LM) is a devastating complication of advanced non-small cell lung cancer (NSCLC). Its diagnosis and monitoring can be challenging. Recently, extracellular vesicle (EV) miRNAs have become a new noninvasive diagnostic biomarker. The purpose of this study was to examine the clinical value and role of EV miRNAs in NSCLC-LM. Next-generation sequencing analysis revealed that miRNAs with differential expression of EVs in sera of patients with NSCLC with LM and non-LM were detected to identify biological markers for the diagnosis of LM. Cellular and in vivo experiments were conducted to explore the pathogenesis of EV miRNA promoting LM in NSCLC. In the present study, we first demonstrated that the serum level of EV-associated miR-374a-5p in patients with LM of lung cancer was much higher than that in patients without LM and was correlated with the survival time of patients with LM. Further studies showed that EV miR-374a-5p efficiently destroys tight junctions and the integrity of the cerebral microvascular endothelial cell barrier, resulting in increased blood-brain barrier permeability. Mechanistically, miR-374a-5p regulates the distribution of ZO1 and occludin in endothelial cells by targeting γ-adducin, increasing vascular permeability and promoting LM. Implications: These results suggest that serum NSCLC-derived EV miR-374a-5p is involved in premetastatic niche formation by regulating the permeability of the blood-brain barrier to promote NSCLC-LM and can be used as a blood biomarker for the diagnosis and prognosis of NSCLC-LM.

Indexed as

Blood-Brain BarrierCarcinoma, Non-Small-Cell LungExtracellular VesiclesLung NeoplasmsMicroRNAsAnimalsCell Line, TumorFemaleHumansMaleMeningeal NeoplasmsMiceMice, NudeMiddle AgedPermeabilityMicroRNAsMIRN374 microRNA 374, human

Identifiers

PMID38639925
PMCPMC11294816
OpenAlexW4394952712

What OpenQuestion holds

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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.