Evidence map›Paper›PMID 28574594›Full record

ArticleBiotechnology and bioengineering2017

A novel protein-engineered hepatocyte growth factor analog released via a shear-thinning injectable hydrogel enhances post-infarction ventricular function.

Amanda N Steele, Lei Cai, Vi N Truong, Bryan B Edwards, Andrew B Goldstone, Anahita Eskandari, Aaron C Mitchell, Laura M Marquardt, Abbygail A Foster, Jennifer R Cochran and 2 more

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.7field-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, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. [Advances in hydrogel drug delivery systems for myocardial infarction treatment].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. AnACS nano · 2019
    Article
  14. Self-Healing Hydrogels: The Next Paradigm Shift in Tissue Engineering?Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    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

12 authors at 1 institution in 1 country.

Amanda N SteeleDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.ORCID 0000-0002-9872-5442
Lei CaiDepartment of Materials Science and Engineering, Stanford University, Stanford, California, 94305.
Vi N TruongDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.
Bryan B EdwardsDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.
Andrew B GoldstoneDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.
Anahita EskandariDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.
Aaron C MitchellDepartment of Bioengineering, Stanford University, Stanford, California, 94305.
Laura M MarquardtDepartment of Materials Science and Engineering, Stanford University, Stanford, California, 94305.
Abbygail A FosterDepartment of Materials Science and Engineering, Stanford University, Stanford, California, 94305.
Jennifer R CochranDepartment of Bioengineering, Stanford University, Stanford, California, 94305.
Sarah C HeilshornDepartment of Bioengineering, Stanford University, Stanford, California, 94305.
Y Joseph WooDepartment of Cardiothoracic Surgery, Stanford University, Stanford, California, 94305.
Stanford University · US

Funding

ANGIOGENIC TISSUE ENGINEERING TO LIMIT POST-INFARCTION VENTRICULAR REMODELINGR01HL089315 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI WOO, Y JOSEPH · 2008 to 2023
$6.4M
T32 Training Program in Mechanisms and Innovation in Vascular DiseaseT32HL098049 · NHLBI · STANFORD UNIVERSITY · PI Nicholas James Leeper, Philip S Tsao · 2010 to 2026
$6.3M
Graduate Training Program in BiotechnologyT32GM008412 · NIGMS · STANFORD UNIVERSITY · PI COCHRAN, JENNIFER R · 1991 to 2020
$5.5M
Engineered HGF-NK1 antagonists for Met-targeted cancer imaging and therapyR01CA151706 · NCI · STANFORD UNIVERSITY · PI COCHRAN, JENNIFER R · 2010 to 2014
$1.6M
Injectable Hydrogels to Improve the Efficacy of iPSC-derived TherapiesR21EB020235 · NIBIB · STANFORD UNIVERSITY · PI HEILSHORN, SARAH C, HUANG, NGAN F. · 2015 to 2016
$433k
NCI NIH HHS R01 CA151706NHLBI NIH HHS R01 HL089315NHLBI NIH HHS T32 HL098049NIBIB NIH HHS R21 EB020235NIGMS NIH HHS T32 GM008412
6 · The paper itself

Abstract

In the last decade, numerous growth factors and biomaterials have been explored for the treatment of myocardial infarction (MI). While pre-clinical studies have demonstrated promising results, clinical trials have been disappointing and inconsistent, likely due to poor translatability. In the present study, we investigate a potential myocardial regenerative therapy consisting of a protein-engineered dimeric fragment of hepatocyte growth factor (HGFdf) encapsulated in a shear-thinning, self-healing, bioengineered hydrogel (SHIELD). We hypothesized that SHIELD would facilitate targeted, sustained intramyocardial delivery of HGFdf thereby attenuating myocardial injury and post-infarction remodeling. Adult male Wistar rats (n = 45) underwent sham surgery or induction of MI followed by injection of phosphate buffered saline (PBS), 10 μg HGFdf alone, SHIELD alone, or SHIELD encapsulating 10 μg HGFdf. Ventricular function, infarct size, and angiogenic response were assessed 4 weeks post-infarction. Treatment with SHIELD + HGFdf significantly reduced infarct size and increased both ejection fraction and borderzone arteriole density compared to the controls. Thus, sustained delivery of HGFdf via SHIELD limits post-infarction adverse ventricular remodeling by increasing angiogenesis and reducing fibrosis. Encapsulation of HGFdf in SHIELD improves clinical translatability by enabling minimally-invasive delivery and subsequent retention and sustained administration of this novel, potent angiogenic protein analog. Biotechnol. Bioeng. 2017;114: 2379-2389. © 2017 Wiley Periodicals, Inc.

Indexed as

Angiogenic ProteinsAnimalsDelayed-Action PreparationsDiffusionHepatocyte Growth FactorHydrogelsInjectionsMaleMyocardial InfarctionProtein EngineeringRatsRats, Sprague-DawleyRats, WistarRecombinant ProteinsShear StrengthTreatment OutcomeAngiogenic ProteinsDelayed-Action PreparationsHepatocyte Growth FactorHydrogelsRecombinant Proteinsangiogenesisgrowth factorhydrogelmyocardial infarctionmyocardial regeneration

Identifiers

PMID28574594
PMCPMC5947314
OpenAlexW2620558514

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.