Evidence map›Paper›PMID 30132374›Full record

ArticleTissue engineering. Part A2019

Nanotechnology Enabled Modulation of Signaling Pathways Affects Physiologic Responses in Intact Vascular Tissue.

Kyle M Hocking, Brian C Evans, Padmini Komalavilas, Joyce Cheung-Flynn, Craig L Duvall, Colleen M Brophy

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Engineering precision nanoparticles for drug delivery.Nature reviews. Drug discovery · 2021
    Review
  6. 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 at 2 institutions in 1 country.

Kyle M Hocking1 Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Brian C Evans1 Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Padmini Komalavilas1 Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Joyce Cheung-Flynn1 Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Craig L Duvall2 Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Colleen M Brophy1 Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

PREVENTION OF VEIN GRAFT SPASMR01HL070715 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BROPHY, COLLEEN M · 2003 to 2021
$7.2M
Substrate Mediated siRNA Delivery from Scaffolds to Promote Wound RepairR01EB019409 · NIBIB · VANDERBILT UNIVERSITY · PI Craig Lewis Duvall · 2014 to 2026
$4.0M
MK2 Inhibitory Nanoplexes to Enhance Long-Term Vascular Graft PatencyR01HL122347 · NHLBI · VANDERBILT UNIVERSITY · PI DUVALL, CRAIG LEWIS · 2016 to 2020
$2.2M
NHLBI NIH HHS R01 HL070715NHLBI NIH HHS R01 HL122347NIBIB NIH HHS R01 EB019409
6 · The paper itself

Abstract

impact statementSubarachnoid hemorrhage (SAH) is associated with vasospasm that is refractory to traditional vasodilators, and inhibition of vasospasm after SAH remains a large unmet clinical need. SAH causes changes in the phosphorylation state of the small heat shock proteins (HSPs), HSP20 and HSP27, in the vasospastic vessels. In this study, the levels of HSP27 and HSP20 were manipulated using nanotechnology to mimic the intracellular phenotype of SAH-induced vasospasm, and the effect of this manipulation was tested on vasomotor responses in intact tissues. This work provides insight into potential therapeutic targets for the development of more effective treatments for SAH induced vasospasm.

Indexed as

Signal TransductionActin CytoskeletonActinsAnimalsBlood VesselsCalciumGene SilencingHeat-Shock ProteinsHumansMicellesMuscle ContractionMuscle, SmoothNanoparticlesNanotechnologyPeptidesPolymerizationActinsCalciumHeat-Shock ProteinsMicellesPeptidesRNA, Small Interferingendosomolytic polymerHSP20HSP27nanotechnologysmooth muscle contractionsubarachnoid hemorrhage

Identifiers

PMID30132374
PMCPMC6450456
OpenAlexW2898204486

What Socratic holds

Textmetadata
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 Socratic graph.