Evidence map›Paper›PMID 38106451›Full record

ReviewInternational journal of nanomedicine2023

A Comprehensive Review of Small Interfering RNAs (siRNAs): Mechanism, Therapeutic Targets, and Delivery Strategies for Cancer Therapy.

Jiaying Zhang, Bo Chen, Chunyuan Gan, Hongyan Sun, Jiaxin Zhang, Lin Feng

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
18.6field-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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

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  20. CRISPR Interference to Inhibit Oncogenes for Cancer Therapy.International journal of molecular sciences · 2026
    Review

18 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Jiaying Zhang *School of Mechanical Engineering and Automation, Beihang University, Beijing, 100191, People's Republic of China.
Bo Chen *School of Mechanical Engineering and Automation, Beihang University, Beijing, 100191, People's Republic of China.
Chunyuan GanSchool of Mechanical Engineering and Automation, Beihang University, Beijing, 100191, People's Republic of China.ORCID 0000-0002-6451-5818
Hongyan SunSchool of Mechanical Engineering and Automation, Beihang University, Beijing, 100191, People's Republic of China.
Jiaxin ZhangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, People's Republic of China.
Lin FengSchool of Mechanical Engineering and Automation, Beihang University, Beijing, 100191, People's Republic of China.
Beihang University · CNBeijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small interfering RNA (siRNA) delivery by nanocarriers has been identified as a promising strategy in the study and treatment of cancer. Short nucleotide sequences are synthesized exogenously to create siRNA, which triggers RNA interference (RNAi) in cells and silences target gene expression in a sequence-specific way. As a nucleic acid-based medicine that has gained popularity recently, siRNA exhibits novel potential for the treatment of cancer. However, there are still many obstacles to overcome before clinical siRNA delivery devices can be developed. In this review, we discuss prospective targets for siRNA drug design, explain siRNA drug properties and benefits, and give an overview of the current clinical siRNA therapeutics for the treatment of cancer. Additionally, we introduce the siRNA chemical modifications and delivery systems that are clinically sophisticated and classify bioresponsive materials for siRNA release in a methodical manner. This review will serve as a reference for researchers in developing more precise and efficient targeted delivery systems, promoting ongoing advances in clinical applications.

Indexed as

NeoplasmsDrug DesignGenetic TherapyHumansRNA InterferenceRNA, Small InterferingRNA, Small Interferingbioresponsive materialscancerchemical modificationsdelivery systemssmall interfering RNA

Identifiers

PMID38106451
PMCPMC10725753
OpenAlexW4389608707

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.