Evidence map›Paper›PMID 40060761›Full record

ReviewBioengineering & translational medicine2025

Unleashing the potential of mRNA: Overcoming delivery challenges with nanoparticles.

Qiang Chen, Ku-Geng Huo, Sheng-Min Ji, Shu-De Pang, Tian-Ying Sun, Yi Niu, Zi-Hao Jiang, Peng Zhang, Shu-Xin Han, Jin-Yao Li

Abstract readReview
In one paragraph

Review in Bioengineering & translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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.

Qiang ChenXinjiang Key Laboratory of Biological Resources and Genetic Engineering College of Life Science & Technology, Xinjiang University Urumqi China.ORCID https://orcid.org/0009-0005-3500-6634
Ku-Geng HuoCyagen Biosciences (Guangzhou) Inc. Guangzhou Guangdong China.
Sheng-Min JiSchool of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation, Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong Yantai University Yantai China.
Shu-De PangDepartment of Pharmaceutics School of Pharmacy, Qingdao University Qingdao China.
Tian-Ying SunSchool of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation, Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong Yantai University Yantai China.
Yi NiuXinjiang Key Laboratory of Biological Resources and Genetic Engineering College of Life Science & Technology, Xinjiang University Urumqi China.
Zi-Hao JiangXinjiang Key Laboratory of Biological Resources and Genetic Engineering College of Life Science & Technology, Xinjiang University Urumqi China.
Peng ZhangSchool of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation, Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong Yantai University Yantai China.
Shu-Xin HanXinjiang Key Laboratory of Biological Resources and Genetic Engineering College of Life Science & Technology, Xinjiang University Urumqi China.
Jin-Yao LiXinjiang Key Laboratory of Biological Resources and Genetic Engineering College of Life Science & Technology, Xinjiang University Urumqi China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Messenger RNA (mRNA) has emerged as a promising therapeutic strategy for various diseases, including cancer, infectious diseases, and genetic disorders. The mRNA-based therapeutics have gained significant attention due to their ability to regulate targeted cells, activate immune cells, and avoid potential risks associated with DNA-based technology. However, the clinical application of mRNA in cancer therapy is hindered by the instability of RNA, physiological barriers, and the risk of immunogenic hurdles. To overcome these challenges and ensure the safe delivery of mRNA therapeutics to target sites, nanoparticle-based delivery systems have been explored as potential tools in vitro and in vivo applications. This review provides a comprehensive overview of the current status of mRNA therapy, discussing its advantages and limitations, delivery strategies and materials, as well as applications in different fields. By exploring these aspects, the researcher can gain a more complete understanding of the current state, prospects, and challenges of mRNA technologies.

Indexed as

delivery strategymRNAnanomaterialnanotechnology

Identifiers

PMID40060761
PMCPMC11883111

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.