Evidence map›Paper›PMID 36361673›Full record

ReviewInternational journal of molecular sciences2022

Self-Amplifying RNA Approach for Protein Replacement Therapy.

Dimitri Papukashvili, Nino Rcheulishvili, Cong Liu, Yang Ji, Yunjiao He, Peng George Wang

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Towards mRNA therapeutics 2.0.Nature reviews. Drug discovery · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. "More" Artificial mRNAs: Beyond the Art of Nature.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  6. RNA-Based Therapies for Inherited Metabolic Disorders.Journal of inherited metabolic disease · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Frontiers in immunology · 2026
    Review
  11. Target, silence, replace: a review on RNA-based drugs in modern medicine.Frontiers in cell and developmental biology · 2026
    Review
  12. Review
  13. The strategies and advances of mRNA translation booster.Asian journal of pharmaceutical sciences · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

6 authors.

Dimitri PapukashviliDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0002-4793-2636
Nino RcheulishviliDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0001-5982-8230
Cong LiuDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Yang JiDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Yunjiao HeDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.
Peng George WangDepartment of Pharmacology, School of Medicine, Southern University of Science and Technology, Shenzhen 518000, China.ORCID 0000-0003-3335-6794

Funding

Shenzhen Science and Technology Innovation Program KQTD20200909113758004
6 · The paper itself

Abstract

Messenger RNA (mRNA) technology has already been successfully tested preclinically and there are ongoing clinical trials for protein replacement purposes; however, more effort has been put into the development of prevention strategies against infectious diseases. Apparently, mRNA vaccine approval against coronavirus disease 2019 (COVID-19) is a landmark for opening new opportunities for managing diverse health disorders based on this approach. Indeed, apart from infectious diseases, it has also been widely tested in numerous directions including cancer prevention and the treatment of inherited disorders. Interestingly, self-amplifying RNA (saRNA)-based technology is believed to display more developed RNA therapy compared with conventional mRNA technique in terms of its lower dosage requirements, relatively fewer side effects, and possessing long-lasting effects. Nevertheless, some challenges still exist that need to be overcome in order to achieve saRNA-based drug approval in clinics. Hence, the current review discusses the feasibility of saRNA utility for protein replacement therapy on various health disorders including rare hereditary diseases and also provides a detailed overview of saRNA advantages, its molecular structure, mechanism of action, and relevant delivery platforms.

Indexed as

COVID-19RNAHumansmRNA VaccinesRNA, MessengerVaccines, SyntheticmRNA VaccinesRNARNA, MessengerVaccines, SyntheticAATDalpha-1 antitrypsin deficiencymRNAprotein deficiencyprotein replacementsaRNAsingle-gene disorderstaRNA

Identifiers

PMID36361673
PMCPMC9655356

What OpenQuestion holds

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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.