Evidence map›Paper›PMID 26878059›Full record

ArticleACS biomaterials science & engineering2016

Biomimetic molecules lower catabolic expression and prevent chondroitin sulfate degradation in an osteoarthritic ex vivo model.

Shaili Sharma, Nelda Vazquez-Portalatin, Sarah Calve, Alyssa Panitch

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Biomimetic strategies for the deputization of proteoglycan functions.Frontiers in cell and developmental biology · 2024
    Review
  7. Proteoglycans and proteoglycan mimetics for tissue engineering.American journal of physiology. Cell physiology · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Senescent cells and osteoarthritis: a painful connection.The Journal of clinical investigation · 2018
    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

4 authors at 1 institution in 1 country.

Shaili Sharma206 S Martin Jischke Drive, Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47907.
Nelda Vazquez-Portalatin206 S Martin Jischke Drive, Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47907.
Sarah Calve206 S Martin Jischke Drive, Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47907.
Alyssa Panitch206 S Martin Jischke Drive, Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47907.
Purdue University West Lafayette · US

Funding

Investigation of Proteoglycan Mimetics as Treatments for OsteoarthritisR01AR065398 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PANITCH, ALYSSA · 2014 to 2018
$1.4M
NIAMS NIH HHS R01 AR065398
6 · The paper itself

Abstract

Aggrecan, the major proteoglycan in cartilage, serves to protect cartilage tissue from damage and degradation during the progression of osteoarthritis (OA). In cartilage extracellular matrix (ECM) aggrecan exists in an aggregate composed of several aggrecan molecules that bind to a single filament of hyaluronan. Each molecule of aggrecan is composed of a protein core and glycosaminoglycan sides chains, the latter of which provides cartilage with the ability to retain water and resist compressive loads. During the progression of OA, loss of aggrecan is considered to occur first, after which other cartilage matrix components become extremely susceptible to degradation. Proteolytic cleavage of the protein core of aggrecan by enzymes such as aggrecanases, prevent its binding to HA and lower cartilage mechanical strength. Here we present the use of HA-binding or collagen type II-binding molecules that functionally mimic aggrecan but lack known cleavage sites, protecting the molecule from proteolytic degradation. These molecules synthesized with chondroitin sulfate backbones conjugated to hyaluronan- or collagen type II- binding peptides, are capable of diffusing through a cartilage explant and adhering to the ECM of this tissue. The objective of this study was to test the functional efficacy of these molecules in an

Indexed as

cartilage matrix degradationChondroitin sulfatecollagen type IIhyaluronanintra-articularresist proteases

Identifiers

PMID26878059
PMCPMC4749183
OpenAlexW2225476181

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.