Evidence map›Paper›PMID 17252549›Full record

ArticleJournal of biomedical materials research. Part A2007

Selective cell proliferation can be controlled with CPC particle coatings.

J A Szivek, D S Margolis, A B Schnepp, W A Grana, S K Williams

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2007. 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
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  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

5 authors at 2 institutions in 1 country.

J A SzivekOrthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Arizona, Tucson, Arizona, USA. szivek@u.arizona.edu
D S Margolis
A B Schnepp
W A Grana
S K Williams
University of Arizona · USTucson Orthopaedic Institute · US

Funding

Sensate Scaffolds for Orthopaedic Tissue RepairR01EB000660 · NIBIB · UNIVERSITY OF ARIZONA · PI SZIVEK, JOHN A · 2002 to 2005
$1.2M
NIBIB NIH HHS R01 EB000660
6 · The paper itself

Abstract

To develop implantable, engineered, cartilage constructs supported by a scaffold, techniques to encourage rapid tissue growth into, and on the scaffold are essential. Preliminary studies indicated that human endothelial cells proliferated at different rates on different calcium phosphate ceramic (CPC) particles. Judicious selection of particles may encourage specific cell proliferation, leading to an ordered growth of tissues for angiogenesis, osteogenesis, and chondrogenesis. The goal of this study was to identify CPC surfaces that encourage bone and vascular cell growth, and other surfaces that support chondrocyte growth while inhibiting proliferation of vascular cells. Differences in bone and vascular cell proliferation were observed when using epoxy without embedded CPCs to encourage bone cells, and when three CPCs were tested, which encouraged vascular cell proliferation. One of these (CPC 7) also substantially depressed cartilage cell proliferation. Only one small-diameter crystalline CPC (CPC 2) supported rapid chondrocyte proliferation, and maintained the cartilage cell phenotype.

Indexed as

Bone and BonesCalcium PhosphatesCell ProliferationCells, CulturedCeramicsEndothelial CellsHumansProteoglycansSurface PropertiesX-Ray Diffractioncalcium phosphateCalcium PhosphatesProteoglycans

Identifiers

PMID17252549
PMCPMC2288747
OpenAlexW2139973539

What OpenQuestion holds

Textmetadata
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.