Evidence map›Paper›PMID 32071240›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

GDF11 promotes osteogenesis as opposed to MSTN, and follistatin, a MSTN/GDF11 inhibitor, increases muscle mass but weakens bone.

Joonho Suh, Na-Kyung Kim, Seung-Hoon Lee, Je-Hyun Eom, Youngkyun Lee, Joo-Cheol Park, Kyung Mi Woo, Jeong-Hwa Baek, Jung-Eun Kim, Hyun-Mo Ryoo and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 81 citations in OpenAlex.

  1. Genes · 2025
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  13. Rethinking Osteoporosis Drugs: Can We Simultaneously Address Sarcopenia?International journal of molecular sciences · 2025
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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

12 authors at 2 institutions in 2 countries.

Joonho SuhDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Na-Kyung KimDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Seung-Hoon LeeDepartment of Molecular Medicine, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu 41566, Republic of Korea.
Je-Hyun EomDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Youngkyun LeeDepartment of Biochemistry, School of Dentistry, Kyungpook National University, Daegu 41566, Republic of Korea.
Joo-Cheol ParkDepartment of Oral Histology-Developmental Biology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Kyung Mi WooDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.ORCID 0000-0002-2782-1189
Jeong-Hwa BaekDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Jung-Eun KimDepartment of Molecular Medicine, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Daegu 41566, Republic of Korea.
Hyun-Mo RyooDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
Se-Jin LeeThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032.
Yun-Sil LeeDepartment of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 08826, Republic of Korea; yunlee@snu.ac.kr.ORCID 0000-0002-1228-0404
Seoul National University · KRUniversity of Connecticut · US

Funding

Characterization of Myostatin and GDF-11R01AR060636 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEE, SE-JIN · 2010 to 2020
$3.7M
TGF-beta family members and their binding proteins in aging skeletal muscleR01AG052962 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEE, SE-JIN, RANDO, THOMAS A. · 2017 to 2020
$1.9M
NIAMS NIH HHS R01 AR060636NIA NIH HHS R01 AG052962
6 · The paper itself

Abstract

Growth and differentiation factor 11 (GDF11) and myostatin (MSTN) are closely related transforming growth factor β (TGF-β) family members, but their biological functions are quite distinct. While MSTN has been widely shown to inhibit muscle growth, GDF11 regulates skeletal patterning and organ development during embryogenesis. Postnatal functions of GDF11, however, remain less clear and controversial. Due to the perinatal lethality of

Indexed as

AnimalsBone and BonesBone Morphogenetic ProteinsChondrocytesDown-RegulationFollistatinGene Expression Regulation, DevelopmentalGrowth Differentiation FactorsMiceMice, KnockoutMuscle DevelopmentMusclesMyostatinOsteoblastsOsteogenesisSignal TransductionBone Morphogenetic ProteinsFollistatinGdf11 protein, mouseGrowth Differentiation FactorsMstn protein, mouseMyostatinTransforming Growth Factor betaBMPfollistatinGDF11myostatinosteogenesis

Identifiers

PMID32071240
PMCPMC7060712
OpenAlexW3008123732

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.