Evidence map›Paper›PMID 37332071›Full record

ReviewMolecular biotechnology2024

MicroRNA-425: A Pivotal Regulator Participating in Tumorigenesis of Human Cancers.

Pouriya Sameti, Mohammad Amini, Fatemeh Oroojalian, Yalda Baghay Esfandyari, Maryam Tohidast, Seyed Ali Rahmani, Shirin Azarbarzin, Ahad Mokhtarzadeh, Behzad Baradaran

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Pouriya SametiDepartment of Biology, Higher Education Institute of Rab-Rashid, Tabriz, Iran.
Mohammad AminiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Fatemeh OroojalianDepartment of Advanced Technologies, School of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.
Yalda Baghay EsfandyariImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Maryam TohidastImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Seyed Ali RahmaniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Shirin AzarbarzinDepartment of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.
Ahad MokhtarzadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. mokhtarzadehah@tbzmed.ac.ir.ORCID http://orcid.org/0000-0002-4515-8675
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. baradaranb@tbzmed.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small single-stranded regulatory RNAs that are shown to be dysregulated in a wide array of human cancers. MiRNAs play critical roles in cancer progression and function as either oncogenes or tumor suppressors through modulating various target genes. Therefore, they possess great potential as diagnostic and therapeutic targets for cancer detection and treatment. In particular, recent studies have illustrated that miR-425 is also dysregulated in various human malignancies and plays a fundamental role in cancer initiation and progression. miR-425 has been reported to function as a dual-role miRNA participating in the regulation of cellular processes, including metastasis, invasion, and cell proliferation by modulating multiple signaling pathways, such as TGF-β, Wnt, and P13K/AKT pathways. Therefore, regarding recent researches showing the high therapeutic potential of miR-425, in this review, we have noted the impact of its dysregulation on signaling pathways and various aspects of tumorigenesis in a variety of human cancers.

Indexed as

CarcinogenesisGene Expression Regulation, NeoplasticMicroRNAsNeoplasmsSignal TransductionAnimalsCell ProliferationHumansMicroRNAsMIRN425 microRNA, humanCancerMicroRNA-425Signaling pathways

Identifiers

What Socratic 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 Socratic graph.