Evidence map›Paper›PMID 29446616›Full record

ArticleBioconjugate chemistry2018

New Mechanism for Release of Endosomal Contents: Osmotic Lysis via Nigericin-Mediated K

Loganathan Rangasamy, Venkatesh Chelvam, Ananda Kumar Kanduluru, Madduri Srinivasarao, N Achini Bandara, Fei You, Esteban A Orellana, Andrea L Kasinski, Philip S Low

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  8. Review
  9. Application of impedance measurement to investigate in vitro inhalation toxicity of bacteria.Journal of occupational medicine and toxicology (London, England) · 2021
    Article
  10. Review
  11. Article
  12. Engineering Targeting Materials for Therapeutic Cancer Vaccines.Frontiers in bioengineering and biotechnology · 2020
    Review
  13. Article
  14. Article
  15. 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

9 authors at 2 institutions in 2 countries.

Loganathan RangasamyPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.
Venkatesh ChelvamPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.
Ananda Kumar KanduluruPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.ORCID 0000-0003-2669-8665
Madduri SrinivasaraoPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.
N Achini BandaraPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.
Fei YouEndocyte, Inc. , 3000 Kent Avenue, Suite A1-100 , West Lafayette , Indiana 47906 , United States.
Esteban A OrellanaDepartment of Biological Sciences, Bindley Bioscience Center , Purdue University , West Lafayette , Indiana 47907 , United States.
Andrea L KasinskiDepartment of Biological Sciences, Bindley Bioscience Center , Purdue University , West Lafayette , Indiana 47907 , United States.
Philip S LowPurdue Institute for Drug Discovery , 720 Clinic Drive , West Lafayette Indiana 47907 , United States.ORCID 0000-0001-9042-5528
Purdue University West Lafayette · USEndocyte (United States) · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Ligand-mediated, vehicle-free delivery of small RNAsR01CA226259 · NCI · PURDUE UNIVERSITY · PI Andrea L Kasinski · 2018 to 2026
$3.4M
Enhancing miRNA Therapeutics through Vehicle Free DeliveryR01CA205420 · NCI · PURDUE UNIVERSITY · PI Andrea L Kasinski · 2017 to 2026
$2.9M
NCI NIH HHS P30 CA023168NCI NIH HHS R01 CA205420NCI NIH HHS R01 CA226259
6 · The paper itself

Abstract

Although peptides, antibodies/antibody fragments, siRNAs, antisense DNAs, enzymes, and aptamers are all under development as possible therapeutic agents, the breadth of their applications has been severely compromised by their inability to reach intracellular targets. Thus, while macromolecules can often enter cells by receptor-mediated endocytosis, their missions frequently fail due to an inability to escape their entrapping endosomes. In this paper, we describe a general method for promoting release of any biologic material from any entrapping endosome. The strategy relies on the fact that all nascent endosomes contain extracellular (Na

Indexed as

AnimalsCell Line, TumorCytosolEndocytosisEndosomesFluorescent DyesHumansHydrogenIonophoresMiceNigericinOsmosisPotassiumRAW 264.7 CellsRNA, Small InterferingSodiumFluorescent DyesHydrogenIonophoresNigericinPotassiumRNA, Small InterferingSodium

Identifiers

PMID29446616
PMCPMC5926190
OpenAlexW2788752482

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.