Evidence map›Paper›PMID 25916502›Full record

ArticleBiomaterials2015

In situ gelling silk-elastinlike protein polymer for transarterial chemoembolization.

Azadeh Poursaid, Robert Price, Andrea Tiede, Erik Olson, Eugene Huo, Lawrence McGill, Hamidreza Ghandehari, Joseph Cappello

Abstract read
In one paragraph

Article in Biomaterials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. International journal of molecular sciences · 2023
    Article
  9. Review
  10. Material characterization of GPXFrontiers in bioengineering and biotechnology · 2023
    Article
  11. Hydrogel systems for targeted cancer therapy.Frontiers in bioengineering and biotechnology · 2023
    Review
  12. Interventional oncology: new techniques and new devices.The British journal of radiology · 2022
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

8 authors at 4 institutions in 1 country.

Azadeh PoursaidDepartment of Bioengineering, University of Utah, 36 S. Wasatch Dr., Salt Lake City, UT 84112, USA; Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, UT 84112, USA.
Robert PriceDepartment of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA; Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, UT 84112, USA.
Andrea TiedeDepartment of Bioengineering, University of Utah, 36 S. Wasatch Dr., Salt Lake City, UT 84112, USA.
Erik OlsonDepartment of Bioengineering, University of Utah, 36 S. Wasatch Dr., Salt Lake City, UT 84112, USA.
Eugene HuoVeterans Affairs Hospital, Salt Lake City, UT 84108, USA.
Lawrence McGillAssociated Regional and University Pathologists, Salt Lake City, UT 84107, USA.
Hamidreza GhandehariDepartment of Bioengineering, University of Utah, 36 S. Wasatch Dr., Salt Lake City, UT 84112, USA; Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA; Utah Center for Nanomedicine, Nano Institute of Utah, University of Utah, Salt Lake City, UT 84112, USA. Electronic address: hamid.ghandehari@pharm.utah.edu.
Joseph CappelloDepartment of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
University of Utah · USWasatch Molecular (United States) · USUniversity Pathologists · USVeterans Health Administration · US

Funding

Engineering Polymers For Gene Therapy of Head CancerR01CA107621 · NCI · UNIVERSITY OF UTAH · PI GHANDEHARI, HAMID · 2005 to 2014
$2.5M
In-Situ Gelling Protein Polymer Intravascular Embolic Agent for Hepatic CarcinomaR42CA168123 · NCI · THERATARGET · PI CHENEY, DARWIN LEROY, GHANDEHARI, HAMID · 2016 to 2019
$1.5M
In-situ Gelling Protein Polymer Intravascular Embolic Agent for Hepatic CarcinomaR41CA168123 · NCI · THERATARGET · PI GHANDEHARI, HAMID · 2012 to 2012
$100k
Recombinant Polymers for Transarterial Chemoembolization of Liver CancerF30CA176922 · NCI · UNIVERSITY OF UTAH · PI POURSAID, AZADEH · 2013 to 2016
$99k
NCI NIH HHS F30 CA176922NCI NIH HHS R01 CA107621NCI NIH HHS R41 CA168123NCI NIH HHS R42 CA168123
6 · The paper itself

Abstract

Hepatocellular carcinoma annually affects over 700,000 people worldwide and trends indicate increasing prevalence. Patients ineligible for surgery undergo loco-regional treatments such as transarterial chemoembolization (TACE) to selectively target tumoral blood supply. Using a microcatheter, chemotherapeutics are infused followed by an embolic agent, or the drug is encapsulated by the embolic moiety; simultaneously inducing stasis while delivering localized chemotherapy. Presently, several products are used, but no universally accepted system is promoted because very disparate limitations exist. The goal of this investigation was to design and develop in situ gelling recombinant silk-elastinlike protein polymers (SELPs) for TACE. Two SELP compositions, SELP-47K and SELP-815K, with varying lengths of silk and elastin blocks, were investigated to formulate a new embolic that was injectable through commercially available microcatheters. The goal was to develop a composition providing maximal permeation of tumor vasculature while exhibiting effective embolic activity. The SELPs evaluated remain soluble until reaching 37 °C, when irreversible transition ensues forming a solid hydrogel network. SELP-815K formulated at 12% w/w with shear processing demonstrated acceptable rheological properties and clear embolic capability under flow conditions in vitro. A rabbit model showed feasibility of embolization in vivo allowing selective occlusion of lobar hepatic arterial branches.

Indexed as

Chemoembolization, TherapeuticAmino Acid SequenceAnimalsHumansHydrogelsLiverLungMaleMolecular Sequence DataNeoplasmsProteinsRabbitsRecombinant Fusion ProteinsRheologyHydrogelsProteinsRecombinant Fusion ProteinsSELP 815Ksilk-elastinlike protein 47KEmbolizationHepatocellular carcinomaRecombinant polymersTACE

Identifiers

PMID25916502
PMCPMC4429515
OpenAlexW2069832753

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.