Evidence map›Paper›PMID 26141836›Full record

ArticleBiomaterials2015

Nano-hydroxyapatite modulates osteoblast lineage commitment by stimulation of DNA methylation and regulation of gene expression.

Shin-Woo Ha, Hae Lin Jang, Ki Tae Nam, George R Beck

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 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 128 citations in OpenAlex.

  1. Phosphate homeostasis and endocrine regulators.Pediatric nephrology (Berlin, Germany) · 2026
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1 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Shin-Woo HaDepartment of Medicine, Division of Endocrinology Metabolism and Lipids, Emory University, Atlanta, GA 30322, United States.
Hae Lin JangDepartment of Materials Science and Engineering, Seoul National University, Seoul 151-744, Republic of Korea.
Ki Tae NamDepartment of Materials Science and Engineering, Seoul National University, Seoul 151-744, Republic of Korea.
George R BeckThe Atlanta Department of Veterans Affairs Medical Center, Decatur, GA 30033, United States; Department of Medicine, Division of Endocrinology Metabolism and Lipids, Emory University, Atlanta, GA 30322, United States; The Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, United States. Electronic address: george.beck@emory.edu.
Emory University · USSeoul National University · KR

Funding

Inorganic phosphate regulated proliferation, transformation and tumorigenesisR01CA136716 · NCI · EMORY UNIVERSITY · PI BECK, GEORGE R. · 2010 to 2013
$1.2M
Bio-active Nanoparticles and the stimulation of autophagy for improved bone massI01BX002363 · VA · VETERANS HEALTH ADMINISTRATION · PI BECK, GEORGE R. · 2014 to 2017
–
BLRD VA I01 BX002363NCI NIH HHS CA136716NCI NIH HHS R01 CA136716
6 · The paper itself

Abstract

Hydroxyapatite (HA) is the primary structural component of the skeleton and dentition. Under biological conditions, HA does not occur spontaneously and therefore must be actively synthesized by mineralizing cells such as osteoblasts. The mechanism(s) by which HA is actively synthesized by cells and deposited to create a mineralized matrix are not fully understood and the consequences of mineralization on cell function are even less well understood. HA can be chemically synthesized (HAp) and is therefore currently being investigated as a promising therapeutic biomaterial for use as a functional scaffold and implant coating for skeletal repair and dental applications. Here we investigated the biological effects of nano-HAp (10 × 100 nm) on the lineage commitment and differentiation of bone forming osteoblasts. Exposure of early stage differentiating osteoblasts resulted in dramatic and sustained changes in gene expression, both increased and decreased, whereas later stage osteoblasts were much less responsive. Analysis of the promoter region one of the most responsive genes, alkaline phosphatase, identified the stimulation of DNA methylation following cell exposure to nano-HAp. Collectively, the results reveal the novel epigenetic regulation of cell function by nano-HAp which has significant implication on lineage determination as well as identifying a novel potential therapeutic use of nanomaterials.

Indexed as

Alkaline PhosphataseAnimalsBiocompatible MaterialsCell DifferentiationCell LineDNA MethylationDurapatiteEpigenesis, GeneticMesenchymal Stem CellsMiceNanostructuresOsteoblastsOsteogenesisPromoter Regions, GeneticAlkaline PhosphataseBiocompatible MaterialsDurapatiteAlkaline phosphataseGene expressionHydroxyapatiteNanoparticleOsteoblastOsteogenesis

Identifiers

PMID26141836
PMCPMC4508253
OpenAlexW767206837

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.