Evidence map›Paper›PMID 28841567›Full record

ReviewBiomolecular concepts2017

Breaking in and busting out: cell-penetrating peptides and the endosomal escape problem.

Julia C LeCher, Scott J Nowak, Jonathan L McMurry

Open access · hybridAbstract readReview
In one paragraph

Review in Biomolecular concepts, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 109 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. MeCP2 is a naturally supercharged protein with cell membrane transduction capabilities.Protein science : a publication of the Protein Society · 2024
    Article
  9. Endosomal escape: A bottleneck for LNP-mediated therapeutics.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Review
  10. Reprogramming tendon healing: a guide to novel molecular tools.Frontiers in bioengineering and biotechnology · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Characterization of PGuaMolecular pharmaceutics · 2023
    Article
  19. Frontiers in immunology · 2023
    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

3 authors at 1 institution in 1 country.

Julia C LeCher.
Scott J Nowak.
Jonathan L McMurry.
Kennesaw State University · US

Funding

Cell-penetrating peptide-adaptors for intracellular cargo deliveryR15GM120691 · NIGMS · KENNESAW STATE UNIVERSITY · PI MCMURRY, JONATHAN L · 2016 to 2016
$402k
Molecular Mechanism of Akirin Function During MyogenesisR15GM102826 · NIGMS · KENNESAW STATE UNIVERSITY · PI NOWAK, SCOTT JAMES · 2013 to 2013
$310k
NIGMS NIH HHS R15 GM102826NIGMS NIH HHS R15 GM120691
6 · The paper itself

Abstract

Cell-penetrating peptides (CPPs) have long held great promise for the manipulation of living cells for therapeutic and research purposes. They allow a wide array of biomolecules from large, oligomeric proteins to nucleic acids and small molecules to rapidly and efficiently traverse cytoplasmic membranes. With few exceptions, if a molecule can be associated with a CPP, it can be delivered into a cell. However, a growing realization in the field is that CPP-cargo fusions largely remain trapped in endosomes and are eventually targeted for degradation or recycling rather than released into the cytoplasm or trafficked to a desired subcellular destination. This 'endosomal escape problem' has confounded efforts to develop CPP-based delivery methods for drugs, enzymes, plasmids, etc. This review provides a brief history of CPP research and discusses current issues in the field with a primary focus on the endosomal escape problem, for which several promising potential solutions have been developed. Are we on the verge of developing technologies to deliver therapeutics such as siRNA, CRISPR/Cas complexes and others that are currently failing because of an inability to get into cells, or are we just chasing after another promising but unworkable technology? We make the case for optimism.

Indexed as

Cell MembraneCell-Penetrating PeptidesDrug Delivery SystemsEndocytosisEndosomesProtein TransportCell-Penetrating Peptidescell-penetrating peptidesendocytosisendosomal escapeprotein transduction domainsTAT

Identifiers

PMID28841567
PMCPMC5640260
OpenAlexW2746514917

What OpenQuestion holds

Textmetadata
LicenceTDM
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.