Evidence map›Paper›PMID 37951522›Full record

ArticleBone2024

Functional defects in cementoblasts with disrupted bone sialoprotein functional domains, in vitro.

Michael B Chavez, Michelle H Tan, Tamara N Kolli, Natalie L Andras, Brian L Foster

Open access · greenAbstract read
In one paragraph

Article in Bone, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Functions of secretory calcium-binding phosphoproteins in dental mineralization.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Review
  4. Article
  5. Article
  6. The role of bone sialoprotein in bone healing.Journal of structural biology · 2024
    Review
  7. 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.

Michael B ChavezDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH, USA; College of Dentistry, University of Iowa, Iowa City, IA, USA.
Michelle H TanDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH, USA.
Tamara N KolliDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH, USA.
Natalie L AndrasDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH, USA.
Brian L FosterDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH, USA. Electronic address: foster.1004@osu.edu.
The Ohio State University · USUniversity of Iowa · US

Funding

Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
Functions of extracellular matrix proteins in dental and skeletal mineralizationR01DE027639 · NIDCR · OHIO STATE UNIVERSITY · PI Brian Lee Foster · 2019 to 2026
$2.3M
Functional domains of bone sialoprotein in dentoalveolar development and healingF30DE030358 · NIDCR · OHIO STATE UNIVERSITY · PI CHAVEZ, MICHAEL B. · 2021 to 2024
$198k
The Role of Bone Sialoprotein in Modulating Periodontal Development and RepairF30DE032897 · NIDCR · OHIO STATE UNIVERSITY · PI ANDRAS, NATALIE LYNN · 2023 to 2024
$108k
NIDCR NIH HHS F30 DE030358NIDCR NIH HHS F30 DE032897NIDCR NIH HHS R01 DE027639NIDCR NIH HHS T32 DE014320
6 · The paper itself

Abstract

Bone sialoprotein (BSP) is a multifunctional extracellular matrix (ECM) protein present in bone and cementum. Global in vivo ablation of BSP leads to bone mineralization defects, lack of acellular cementum, and periodontal breakdown. BSP harbors three main functional domains: N-terminal collagen-binding domain, hydroxyapatite-nucleating domain, and C-terminal RGD integrin-binding signaling domain. How each of these domains contributes to BSP function(s) is not understood. We hypothesized that collagen-binding and RGD domains play distinct roles in cementoblast functions. Three CRISPR/Cas9 gene-edited cell lines were derived from control wild-type (WT) OCCM.30 murine immortalized cementoblasts: 1) deletion of the N-terminus of BSP after signal peptide, including entire collagen binding domain (Ibsp

Indexed as

Dental CementumExtracellular Matrix ProteinsAnimalsCollagenIntegrin-Binding SialoproteinIntegrinsMiceOligopeptidesCollagenExtracellular Matrix ProteinsIntegrin-Binding SialoproteinIntegrinsOligopeptidesBone biologyBone remodeling/regenerationExtracellular matrix (ECM)Mineralized tissue/developmentOsteoblast(s)

Identifiers

PMID37951522
PMCPMC10841848
OpenAlexW4388573772

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.