Evidence map›Paper›PMID 28842318›Full record

ReviewJournal of controlled release : official journal of the Controlled Release Society2017

Stimulus-responsive viral vectors for controlled delivery of therapeutics.

Mitchell J Brun, Eric J Gomez, Junghae Suh

Abstract readReview
In one paragraph

Review in Journal of controlled release : official journal of the Controlled Release Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Designing molecules: directing stem cell differentiation.Frontiers in bioengineering and biotechnology · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. Plant Virus Nanoparticles for Anti-cancer Therapy.Frontiers in bioengineering and biotechnology · 2021
    Review
  8. Article
  9. Biodegradable Polymers for Gene Delivery.Molecules (Basel, Switzerland) · 2019
    Review
  10. Reducing off target viral delivery in ovarian cancer gene therapy using a protease-activated AAV2 vector platform.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Article
  11. Physical, chemical, and synthetic virology: Reprogramming viruses as controllable nanodevices.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2019
    Review
  12. Article
  13. Article
  14. 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.

Mitchell J BrunDepartment of Chemical and Biomolecular Engineering, Rice University, Houston, TX, United States.
Eric J GomezDepartment of Bioengineering, Rice University, Houston, TX, United States.
Junghae SuhDepartment of Bioengineering, Rice University, Houston, TX, United States; Systems, Synthetic, and Physical Biology Program, Rice University, Houston, TX, United States. Electronic address: jsuh@rice.edu.
Rice University · US

Funding

Provectors for treatment of ovarian cancerR01CA207497 · NCI · RICE UNIVERSITY · PI BAO, GANG, SUH, JUNGHAE · 2016 to 2020
$1.8M
MMP-targeted viral gene delivery vectors for treatment of infarcted heartR21HL126053 · NHLBI · RICE UNIVERSITY · PI SUH, JUNGHAE · 2015 to 2016
$428k
Matrilysin-Sensing Gene Delivery Vectors for Colorectal Cancer TherapyR21CA187316 · NCI · RICE UNIVERSITY · PI SUH, JUNGHAE · 2014 to 2015
$381k
NCI NIH HHS R01 CA207497NCI NIH HHS R21 CA187316NHLBI NIH HHS R21 HL126053
6 · The paper itself

Abstract

Virus-based therapies have gained momentum as the next generation of treatments for a variety of serious diseases. In order to make these therapies more controllable, stimulus-responsive viral vectors capable of sensing and responding to specific environmental inputs are currently being developed. A number of viruses naturally respond to endogenous stimuli, such as pH, redox, and proteases, which are present at different concentrations in diseases and at different organ and organelle sites. Additionally, rather than relying on natural viral properties, efforts are underway to engineer viruses to respond to endogenous stimuli in new ways as well as to exogenous stimuli, such as temperature, magnetic field, and optical light. Viruses with stimulus-responsive capabilities, either nature-evolved or human-engineered, will be reviewed to capture the current state of the field. Stimulus-responsive viral vector design considerations as well as gaps in current research efforts will be identified.

Indexed as

Drug Delivery SystemsVirusesAnimalsHumansHydrogen-Ion ConcentrationOxidation-ReductionPeptide HydrolasesPhysical StimulationPeptide HydrolasesBioactivatableBioresponsiveGene deliveryGene therapyViral vector

Identifiers

PMID28842318
PMCPMC5723212
OpenAlexW2747596278

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.