Evidence map›Paper›PMID 37460924›Full record

ReviewMilitary Medical Research2023

Targeting miRNA by CRISPR/Cas in cancer: advantages and challenges.

Bashdar Mahmud Hussen, Mohammed Fatih Rasul, Snur Rasool Abdullah, Hazha Jamal Hidayat, Goran Sedeeq Hama Faraj, Fattma Abodi Ali, Abbas Salihi, Aria Baniahmad, Soudeh Ghafouri-Fard, Milladur Rahman and 3 more

Open access · diamondAbstract readReview
In one paragraph

Review in Military Medical Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
13.1field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 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

13 authors at 11 institutions in 6 countries.

Bashdar Mahmud HussenDepartment of Biomedical Sciences, Cihan University-Erbil, Erbil, Kurdistan Region, 44001, Iraq.
Mohammed Fatih RasulDepartment of Pharmaceutical Basic Science, Faculty of Pharmacy, Tishk International University, Erbil, Kurdistan Region, 44001, Iraq.
Snur Rasool AbdullahMedical Laboratory Science, Lebanese French University, Erbil, Kurdistan Region, 44001, Iraq.
Hazha Jamal HidayatDepartment of Biology, College of Education, Salahaddin University-Erbil, Erbil, Kurdistan Region, 44001, Iraq.
Goran Sedeeq Hama FarajDepartment of Medical Laboratory Science, Komar University of Science and Technology, Sulaymaniyah, 46001, Iraq.
Fattma Abodi AliDepartment of Medical Microbiology, College of Health Sciences, Hawler Medical University, Erbil, Kurdistan Region, 44001, Iraq.
Abbas SalihiDepartment of Biology, College of Science, Salahaddin University-Erbil, Erbil, Kurdistan Region, 44001, Iraq.
Aria BaniahmadInstitute of Human Genetics, Jena University Hospital, 07747, Jena, Germany.
Soudeh Ghafouri-FardDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, 374-37515, Iran.
Milladur RahmanDepartment of Clinical Sciences, Malmö, Section for Surgery, Lund University, 22100, Malmö, Sweden.
Mark C GlassyTranslational Neuro-Oncology Laboratory, San Diego (UCSD) Moores Cancer Center, University of California, San Diego, CA, 94720, USA.
Wojciech BranickiFaculty of Biology, Institute of Zoology and Biomedical Research, Jagiellonian University, 31-007, Kraków, Poland. wojciech.branicki@uj.edu.pl.
Mohammad TaheriInstitute of Human Genetics, Jena University Hospital, 07747, Jena, Germany. mohammad.taheri@uni-jena.de.ORCID 0000-0001-8381-0591
Jena University Hospital · DELebanese French University · IQCihan University-Erbil · IQHawler Medical University · IQJagiellonian University · PLKomar University of Science and Technology · IQLund University · SESalahaddin University-Erbil · IQShahid Beheshti University of Medical Sciences · IRTishk International University · IQUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clustered regulatory interspaced short palindromic repeats (CRISPR) has changed biomedical research and provided entirely new models to analyze every aspect of biomedical sciences during the last decade. In the study of cancer, the CRISPR/CRISPR-associated protein (Cas) system opens new avenues into issues that were once unknown in our knowledge of the noncoding genome, tumor heterogeneity, and precision medicines. CRISPR/Cas-based gene-editing technology now allows for the precise and permanent targeting of mutations and provides an opportunity to target small non-coding RNAs such as microRNAs (miRNAs). However, the development of effective and safe cancer gene editing therapy is highly dependent on proper design to be innocuous to normal cells and prevent introducing other abnormalities. This study aims to highlight the cutting-edge approaches in cancer-gene editing therapy based on the CRISPR/Cas technology to target miRNAs in cancer therapy. Furthermore, we highlight the potential challenges in CRISPR/Cas-mediated miRNA gene editing and offer advanced strategies to overcome them.

Indexed as

MicroRNAsNeoplasmsCRISPR-Cas SystemsGene EditingHumansMicroRNAsCancer therapyCRISPRCRISPR/Cas12CRISPR/Cas9Gene editingmiRNAs

Identifiers

PMID37460924
PMCPMC10351202
OpenAlexW4384526098

What OpenQuestion 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 OpenQuestion graph.