Evidence map›Paper›PMID 40735832›Full record

ArticleJournal of cellular and molecular medicine2025

LINC01614: A Potential Therapeutic Target in Astrocytoma Progression.

Fatemeh Karimpour, Mohammad Hosseini Hooshiar, Shima Abbasnejad, Kimia Abdi, Arsalan Jalili, Amir Khanmirzaei, Sara Tutunchi, Amir-Reza Javanmard, Mohammadreza Hajiesmaeili, Sayyed Mohammad Hossein Ghaderian

RetractedAbstract readRetracted Publication
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. LINC01614: A Potential Therapeutic Target in Astrocytoma Progression.Journal of cellular and molecular medicine · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Fatemeh KarimpourCancer Research Center, Health Research institute, Babol University of Medical Sciences, Babol, Iran.
Mohammad Hosseini HooshiarDepartment of Periodontics, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.
Shima AbbasnejadDepartment of Cell and Molecular Biology, Faculty of Chemistry, University of Kashan, Kashan, Iran.
Kimia AbdiDepartment of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Arsalan JaliliIranian Tissue Bank and Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Amir KhanmirzaeiFaculty of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
Sara TutunchiDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Amir-Reza JavanmardDepartment of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.ORCID 0000-0003-1836-8949
Mohammadreza HajiesmaeiliSkull Base Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sayyed Mohammad Hossein GhaderianSkull Base Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astrocytomas are aggressive brain tumours with limited treatment options, making the identification of novel therapeutic targets crucial. Long noncoding RNAs (lncRNAs) have emerged as key regulators of gene expression and have been implicated in various cancers, including astrocytoma. LINC01614 is a lncRNA that has been found to be upregulated in astrocytoma, suggesting its potential role in tumour progression. In this study, we investigated the functional role of LINC01614 in astrocytoma and its interaction with miR-128, a known regulator of the RAS/Map kinase signalling pathway. Through in vitro experimental assays, we demonstrated that LINC01614 upregulation promotes astrocytoma cell proliferation and invasion, potentially through the sponging of miR-128. Furthermore, in silico analysis revealed potential binding sites of miR-128 within the RAS/Map kinase signalling pathway, suggesting a regulatory role for miR-128 in this pathway. Our findings provide novel insights into the molecular mechanisms underlying astrocytoma progression and highlight the potential of LINC01614 as a therapeutic target. Targeting LINC01614 or modulating miR-128 expression may offer new therapeutic strategies for astrocytoma treatment. Additionally, our in silico analysis provides a foundation for further exploration of the regulatory network involving LINC01614, miR-128 and the RAS/Map kinase signalling pathway. Overall, this study sheds light on the intricate regulatory network in astrocytoma and presents promising avenues for the development of targeted therapies for this devastating disease.

Indexed as

AstrocytomaBrain NeoplasmsMicroRNAsRNA, Long NoncodingCell Line, TumorCell MovementCell ProliferationDisease ProgressionGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemNeoplasm InvasivenessSignal TransductionMicroRNAsRNA, Long NoncodingastrocytomaLINC01614miR‐128sponging

Identifiers

PMID40735832
PMCPMC12308213

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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.