Evidence map›Paper›PMID 29505725›Full record

ArticleBiomacromolecules2018

Macromolecule-Network Electrostatics Controlling Delivery of the Biotherapeutic Cell Modulator TIMP-2.

Yuji Yamada, Ananda Chowdhury, Joel P Schneider, William G Stetler-Stevenson

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Peptide hydrogels for affinity-controlled release of therapeutic cargo: Current and potential strategies.Journal of peptide science : an official publication of the European Peptide Society · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. 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

4 authors at 1 institution in 1 country.

Yuji YamadaChemical Biology Laboratory , National Cancer Institute, National Institutes of Health , Frederick , Maryland 21701 , United States.
Ananda ChowdhuryRadiation Oncology Branch , National Cancer Institute, National Institutes of Health , Bethesda , Maryland 20892 , United States.ORCID 0000-0002-2016-3697
Joel P SchneiderChemical Biology Laboratory , National Cancer Institute, National Institutes of Health , Frederick , Maryland 21701 , United States.
William G Stetler-StevensonRadiation Oncology Branch , National Cancer Institute, National Institutes of Health , Bethesda , Maryland 20892 , United States.ORCID 0000-0002-5500-5808
National Institutes of Health · US

Funding

Design and Utility of Novel Protienaceous BiomaterialsZIABC011313 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHNEIDER, JOEL · 2010 to 2025
$19.0M
Preclinical development of TIMP-2 as a biologic therapy for cancerZIABC011204 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI STETLER-STEVENSON, WILLIAM · 2009 to 2024
$14.5M
The Role of TIMPs in Cell Growth, Tumor Progression and MetastasisZIASC009179 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI STETLER-STEVENSON, WILLIAM · 2009 to 2024
$9.7M
Tissue Inhibitors of Metalloproteinases: Regulation of CZ01SC009179 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI STETLER-STEVENSON, WILLIAM G · 1996 to 2008
$3.4M
Intramural NIH HHS Z01 SC009179NCI NIH HHS ZIA BC011204
6 · The paper itself

Abstract

Tissue inhibitor of metalloproteinase 2 (TIMP-2) is an endogenous 22 kDa proteinase inhibitor, demonstrating antitumorigenic, antimetastatic and antiangiogenic activities in vitro and in vivo. Recombinant TIMP-2 is currently undergoing preclinical testing in multiple, murine tumor models. Here we report the development of an inert, injectable peptide hydrogel matrix enabling encapsulation and sustained release of TIMP-2. We studied the TIMP-2 release profile from four β-hairpin peptide gels of varying net electrostatic charge. A negatively charged peptide gel (designated AcVES3) enabling encapsulation of 4 mg/mL of TIMP-2, without effects on rheological properties, facilitated the slow sustained release (0.9%/d) of TIMP-2 over 28 d. Released TIMP-2 is structurally intact and maintains the ability to inhibit MMP activity, as well as suppress lung cancer cell proliferation in vitro. These findings suggest that the AcVES3 hydrogel will be useful as an injectable vehicle for systemic delivery of TIMP-2 in vivo for ongoing preclinical development.

Indexed as

Gene Transfer TechniquesCell ProliferationHumansHydrogel, Polyethylene Glycol DimethacrylateLung NeoplasmsPeptidesRecombinant ProteinsRheologyStatic ElectricityTissue Inhibitor of Metalloproteinase-2Hydrogel, Polyethylene Glycol DimethacrylatePeptidesRecombinant ProteinsTIMP2 protein, humanTissue Inhibitor of Metalloproteinase-2

Identifiers

PMID29505725
PMCPMC6329387
OpenAlexW2789765872

What OpenQuestion holds

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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.