Evidence map›Paper›PMID 31508439›Full record

ArticleMolecular therapy. Methods & clinical development2019

Optimizing Modified mRNA

Yoav Hadas, Nishat Sultana, Elias Youssef, Mohammad Tofael Kabir Sharkar, Keerat Kaur, Elena Chepurko, Lior Zangi

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.5field-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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Anion exchange HPLC monitoring of mRNAFrontiers in molecular biosciences · 2024
    Article
  6. Large-scale manufacturing of base-edited chimeric antigen receptor T cells.Molecular therapy. Methods & clinical development · 2023
    Article
  7. Article
  8. Modified mRNA as a Treatment for Myocardial Infarction.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Modified mRNA Therapeutics for Heart Diseases.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Review
  13. NScientific reports · 2022
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Modified mRNA as a Therapeutic Tool for the Heart.Cardiovascular drugs and therapy · 2020
    Review
  19. Article
  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

7 authors at 1 institution in 1 country.

Yoav HadasCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Nishat SultanaCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elias YoussefCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mohammad Tofael Kabir SharkarCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Keerat KaurCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Elena ChepurkoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Lior ZangiCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Icahn School of Medicine at Mount Sinai · US

Funding

TRAINING PROGRAM IN MOLECULAR AND CELLULAR CARDIOLOGYT32HL007824 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GELB, BRUCE D · 1995 to 2022
$8.6M
Cardiomyocyte-specific modified mRNA of Pkm2 for induction of cardiac regeneration in ischemic heart failureR01HL142768 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZANGI, LIOR · 2018 to 2022
$2.1M
NHLBI NIH HHS R01 HL142768NHLBI NIH HHS T32 HL007824
6 · The paper itself

Abstract

Synthetic modified RNA (modRNA) is a novel vector for gene transfer to the heart and other organs. modRNA can mediate strong, transient protein expression with minimal induction of the innate immune response and risk for genome integration. modRNA is already being used in several human clinical trials, and its use in basic and translational science is growing. Due to the complexity of preparing modRNA and the high cost of its reagents, there is a need for an improved, cost-efficient protocol to make modRNA. Here we show that changing the ratio between anti-reverse cap analog (ARCA) and N1-methyl-pseudouridine (N1mΨ), favoring ARCA over N1mΨ, significantly increases the yield per reaction, improves modRNA translation, and reduces its immunogenicity

Indexed as

gene therapyin vitro mRNA synthesismodified mRNA

Identifiers

PMID31508439
PMCPMC6722299
OpenAlexW2965853653

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.