Evidence map›Paper›PMID 39456774›Full record

SynthesisInternational journal of molecular sciences2024

Systematic Review of Peptide CAQK: Properties, Applications, and Outcomes.

Jose A Castillo, Michael Nhien Le, Amanda Ratcliff, Khadija Soufi, Kuanwei Huang, Sina Vatoofy, Arash Ghaffari-Rafi, Samuel Emerson, Elizabeth Reynolds, Christopher Pivetti and 6 more

Abstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

16 authors.

Jose A CastilloUC Davis Medical Center, Sacramento, CA 95817, USA.
Michael Nhien LeUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0009-0004-9548-1720
Amanda RatcliffUC Davis Medical Center, Sacramento, CA 95817, USA.
Khadija SoufiUC Davis Medical Center, Sacramento, CA 95817, USA.
Kuanwei HuangUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0000-0002-1937-645X
Sina VatoofyUC Davis Medical Center, Sacramento, CA 95817, USA.
Arash Ghaffari-RafiUC Davis Medical Center, Sacramento, CA 95817, USA.
Samuel EmersonUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0009-0004-6350-3470
Elizabeth ReynoldsUC Davis Medical Center, Sacramento, CA 95817, USA.
Christopher PivettiUC Davis Medical Center, Sacramento, CA 95817, USA.
Kaitlin ClarkUC Davis Medical Center, Sacramento, CA 95817, USA.
Allan MartinUC Davis Medical Center, Sacramento, CA 95817, USA.
Richard PriceUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0000-0002-7261-2028
Kee KimUC Davis Medical Center, Sacramento, CA 95817, USA.
Aijun WangUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0000-0002-2985-3627
Rachel RussoUC Davis Medical Center, Sacramento, CA 95817, USA.ORCID 0000-0002-5971-5508

Funding

Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
NHLBI NIH HHS T32 HL086350
6 · The paper itself

Abstract

Many central nervous system (CNS) disorders lack approved treatment options. Previous research demonstrated that peptide CAQK can bind to chondroitin sulfate proteoglycans (CSPGs) in the extracellular matrix of the CNS. In vivo studies have investigated CAQK conjugated to nanoparticles containing therapeutic agents with varying methodologies/outcomes. This paper presents the first systematic review assessing its properties, applications, and outcomes secondary to its use. Following PRISMA guidelines, a comprehensive search was performed across multiple databases. Studies utilizing CAQK as a therapeutic agent/homing molecule in animal/human models were selected. Sixteen studies met the inclusion criteria. Mice and rats were the predominant animal models. All studies except one used CAQK to deliver a therapeutic agent. The reviewed studies mostly included models of brain and spinal cord injuries. Most studies had intravenous administration of CAQK. All studies demonstrated various benefits and that CAQK conjugation facilitated localization to target tissues. No studies directly evaluated the effects of CAQK alone. The data are limited by the heterogeneity in study methodologies and the lack of direct comparison between CAQK and conjugated agents. Overall, these findings present CAQK utilization to deliver a therapeutic agent as a promising targeting strategy in the management of disorders where CSPGs are upregulated.

Indexed as

PeptidesAnimalsCentral Nervous System DiseasesChondroitin Sulfate ProteoglycansDisease Models, AnimalHumansMiceNanoparticlesRatsSpinal Cord InjuriesChondroitin Sulfate ProteoglycansPeptidesCAQKcentral nervous system targetingintravenous therapy

Identifiers

PMID39456774
PMCPMC11507173

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.