Evidence map›Paper›PMID 28659341›Full record

ArticleThe Journal of biological chemistry2017

Activin receptor type 2A (ACVR2A) functions directly in osteoblasts as a negative regulator of bone mass.

Brian C Goh, Vandana Singhal, Angelica J Herrera, Ryan E Tomlinson, Soohyun Kim, Marie-Claude Faugere, Emily L Germain-Lee, Thomas L Clemens, Se-Jin Lee, Douglas J DiGirolamo

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Rethinking Osteoporosis Drugs: Can We Simultaneously Address Sarcopenia?International journal of molecular sciences · 2025
    Review
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  6. Animal models of tendon calcification: Past, present, and future.Animal models and experimental medicine · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Functional comparison of human ACVR1 and zebrafish Acvr1l FOP-associated variants in embryonic zebrafish.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
  12. Article
  13. Myostatin: A Skeletal Muscle Chalone.Annual review of physiology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

10 authors at 4 institutions in 1 country.

Brian C GohFrom the Departments of Orthopaedic Surgery and.
Vandana SinghalFrom the Departments of Orthopaedic Surgery and.
Angelica J HerreraFrom the Departments of Orthopaedic Surgery and.
Ryan E TomlinsonFrom the Departments of Orthopaedic Surgery and.
Soohyun KimFrom the Departments of Orthopaedic Surgery and.
Marie-Claude Faugerethe Albert B. Chandler Medical Center, University of Kentucky, Lexington, Kentucky 40536.
Emily L Germain-Leethe Department of Pediatrics, University of Connecticut School of Medicine/UConn Health, Farmington, Connecticut 06030.
Thomas L ClemensFrom the Departments of Orthopaedic Surgery and.
Se-Jin LeeMolecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287.
Douglas J DiGirolamoFrom the Departments of Orthopaedic Surgery and ddigiro2@jhmi.edu.
Albert B. Chandler Hospital · USJohns Hopkins University · USUConn Health · USUnited States Department of Veterans Affairs · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
Characterization of Myostatin and GDF-11R01AR060636 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEE, SE-JIN · 2010 to 2020
$3.7M
Activin receptor-based therapies for musculoskeletal diseaseR01AR062074 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI DIGIROLAMO, DOUGLAS JAMES · 2011 to 2015
$2.0M
NIAMS NIH HHS R01 AR060636NIAMS NIH HHS R01 AR062074NIGMS NIH HHS T32 GM007309
6 · The paper itself

Abstract

Bone and skeletal muscle mass are highly correlated in mammals, suggesting the existence of common anabolic signaling networks that coordinate the development of these two anatomically adjacent tissues. The activin signaling pathway is an attractive candidate to fulfill such a role. Here, we generated mice with conditional deletion of activin receptor (ACVR) type 2A, ACVR2B, or both, in osteoblasts, to determine the contribution of activin receptor signaling in regulating bone mass. Immunohistochemistry localized ACVR2A and ACVR2B to osteoblasts and osteocytes. Primary osteoblasts expressed activin signaling components, including ACVR2A, ACVR2B, and ACVR1B (ALK4) and demonstrated increased levels of phosphorylated Smad2/3 upon exposure to activin ligands. Osteoblasts lacking ACVR2B did not show significant changes

Indexed as

OsteogenesisActivin Receptors, Type IIAnimalsAnimals, NewbornBone DevelopmentCell ProliferationCells, CulturedCrosses, GeneticFemaleFemurGene DeletionMaleMice, Inbred C57BLMice, TransgenicMuscle DevelopmentMuscle, SkeletalActivin Receptors, Type IIactivin receptor type II-Aactivin receptor type II-Bactivinbonemyostatinosteoblasttransforming growth factor beta (TGF-β)

Identifiers

PMID28659341
PMCPMC5566533
OpenAlexW2729094506

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.