Evidence map›Paper›PMID 37149609›Full record

ReviewCancer cell international2023

Targeted therapy using nanocomposite delivery systems in cancer treatment: highlighting miR34a regulation for clinical applications.

Muhammad Javed Iqbal, Zeeshan Javed, Haleema Sadia, Sajid Mehmood, Ali Akbar, Benish Zahid, Tariq Nadeem, Sadia Roshan, Elena Maria Varoni, Marcello Iriti and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancer cell international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 20 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 5 countries.

Muhammad Javed IqbalDepartment of Biotechnology, University of Sialkot, Punjab, Pakistan.
Zeeshan JavedCentre for Applied Molecular Biology, University of the Punjab, Lahore, Pakistan.
Haleema SadiaBUITEMS, Quetta, Pakistan.
Sajid MehmoodDepartment of Biochemistry, Islam Medical and Dental College, Sialkot, Pakistan.
Ali AkbarDepartment of Microbiology, University of Balochistan Quetta, Quetta, Pakistan.
Benish ZahidDepartment of Pathobiology, KBCMA, CVAS, Sub Campus University of Veterinary and Animal Sciences, Narowal, Pakistan.
Tariq NadeemNational Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
Sadia RoshanDepartment of Zoology, University of Gujrat, Gujrat, Pakistan.
Elena Maria VaroniDipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche, Università degli Studi di Milano, Milan, Italy.
Marcello IritiDepartment of Agricultural and Environmental Sciences, Università degli Studi di Milano, Milan, Italy.
Eda Sönmez GürerFaculty of Pharmacy, Department of Pharmacognosy, Sivas Cumhuriyet University, Sivas, Turkey.
Javad Sharifi-RadFacultad de Medicina, Universidad del Azuay, Cuenca, Ecuador. javad.sharifirad@gmail.com.
Daniela CalinaDepartment of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, Craiova, 200349, Romania. calinadaniela@gmail.com.
University of Milan · ITBalochistan University of Information Technology, Engineering and Management Sciences · PKCentre of Excellence in Molecular Biology · PKSivas Cumhuriyet Üniversitesi · TRUniversidad del Azuay · ECUniversity of Balochistan · PKUniversity of Gujrat · PKUniversity of Medicine and Pharmacy of Craiova · ROUniversity of SialkotUniversity of the Punjab · PKUniversity of Veterinary and Animal Sciences · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical application of microRNAs in modern therapeutics holds great promise to uncover molecular limitations and conquer the unbeatable castle of cancer metastasis. miRNAs play a decisive role that regulating gene expression at the post-transcription level while controlling both the stability and translation capacity of mRNAs. Specifically, miR34a is a master regulator of the tumor suppressor gene, cancer progression, stemness, and drug resistance at the cell level in p53-dependent and independent signaling. With changing, trends in nanotechnology, in particular with the revolution in the field of nanomedicine, nano drug delivery systems have emerged as a prominent strategy in clinical practices coupled with miR34a delivery. Recently, it has been observed that forced miR34a expression in human cancer cell lines and model organisms limits cell proliferation and metastasis by targeting several signaling cascades, with various studies endorsing that miR34a deregulation in cancer cells modulates apoptosis and thus requires targeted nano-delivery systems for cancer treatment. In this sense, the present review aims to provide an overview of the clinical applications of miR34a regulation in targeted therapy of cancer.

Indexed as

cancer treatmentmiR34ap53 signalingtumorigenesis, nano-delivery systems

Identifiers

PMID37149609
PMCPMC10164299
OpenAlexW4372342208

What Socratic 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 Socratic graph.