Evidence map›Paper›PMID 40694092›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2025

Molecular insight into the therapeutic potential of miR-34a in retinoblastoma.

Pouya Goleij, Mohammad Amin Khazeei Tabari, Aryan Rezaee, Pantea Majma Sanaye, Ali Kheirandish, Khalaf F Alsharif, Maria Daglia, Danaé S Larsen, Haroon Khan, Mohadeseh Poudineh

Abstract readReview
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In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Pouya GoleijUSERN Office, Kermanshah University of Medical Sciences, Kermanshah, 6715847141, Iran. medgenetic.1991@gmail.com.
Mohammad Amin Khazeei TabariStudent Research Committee, School of Medicine, Mazandaran University of Medical Sciences, Sari, 4815733971, Mazandaran, Iran.
Aryan RezaeeSchool of Medicine, Iran University of Medical Sciences, Tehran, 1449614535, Iran.
Pantea Majma SanayeSchool of Pharmacy, Zanjan University of Medical Sciences, Zanjan, 4513956184, Iran.
Ali KheirandishStudent Research Committee, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, 4815733971, Iran.
Khalaf F AlsharifDepartment of Clinical Laboratory Science, College of Applied Medical Science, Taif University, P.O. Box 11099, 21944, Taif, Saudi Arabia.
Maria DagliaInternational Research Center for Food Nutrition and Safety, Jiangsu University, Zhenjiang, 212013, China.
Danaé S LarsenSchool of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland, 1010, New Zealand.
Haroon KhanDepartment of Pharmacy, Faculty of Chemical and Life Sciences, Abdul Wali Khan University Mardan, Mardan, 23200, Pakistan. haroonkhan@awkum.edu.pk.
Mohadeseh PoudinehStudent Research Committee, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinoblastoma (RB) is the predominant type of eye cancer in children, particularly affecting those under three. Early diagnosis is crucial as RB can be fatal if left untreated. MicroRNAs (miRNAs), non-coding RNAs, have emerged as significant regulators of various cellular processes and are increasingly recognized for their influence on RB development and treatment resistance. Dysregulation of miR-34a expression has been implicated in various aspects of tumorigenesis, including processes critical for cancer progression: epithelial-mesenchymal transition (EMT) within the tumor, invasive growth, and metastasis. Furthermore, a deeper understanding of the molecular mechanisms underlying miR-34a function in RB is crucial for the development of effective diagnostic tools and therapeutic strategies. The abundance of miR-34a is further fine-tuned through context-dependent feedback loops. This review comprehensively examines the current understanding of miR-34a's functions in various human diseases. We focus on how miR-34a expression is regulated and disrupted, its involvement in human cancers specifically RB, and its potential as a biomarker for disease diagnosis and prognosis. Additionally, we explore the potential of miR-34a as a novel therapeutic target in RB.

Indexed as

MicroRNAsRetinoblastomaBiomarkers, TumorEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansBiomarkers, TumorMicroRNAsMIRN34 microRNA, humanAngiogenesisCell proliferationmiR-34aRetinoblastomaTherapeuticTumor suppressor

Identifiers

PMID40694092

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.