Evidence map›Paper›PMID 32531191›Full record

ArticleStem cell reports2020

Hedgehog Activation Regulates Human Osteoblastogenesis.

Shoko Onodera, Akiko Saito, Hironori Hojo, Takashi Nakamura, Denise Zujur, Katsuhito Watanabe, Nana Morita, Daigo Hasegawa, Hideki Masaki, Hiromitsu Nakauchi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
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  5. Lipopolysaccharide Impedes Bone Repair inInternational journal of molecular sciences · 2023
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  7. Current Status of Next-Generation Sequencing in Bone Genetic Diseases.International journal of molecular sciences · 2023
    Review
  8. From mesenchymal niches to engineeredMaterials today. Bio · 2022
    Article
  9. Review
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  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

16 authors at 4 institutions in 2 countries.

Shoko OnoderaDepartment of Biochemistry, Tokyo Dental College, Tokyo 101-0061, Japan; Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8656, Japan.
Akiko SaitoDepartment of Biochemistry, Tokyo Dental College, Tokyo 101-0061, Japan.
Hironori HojoCenter for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8656, Japan; Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8655, Japan.
Takashi NakamuraDepartment of Biochemistry, Tokyo Dental College, Tokyo 101-0061, Japan.
Denise ZujurCenter for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8656, Japan.
Katsuhito WatanabeDepartment of Oral and Maxillofacial Surgery, Tokyo Dental College, Tokyo 101-0061, Japan.
Nana MoritaDepartment of Oral Medicine, Oral and Maxillofacial Surgery, Tokyo Dental College, Chiba 272-8513, Japan.
Daigo HasegawaDepartment of Oral and Maxillofacial Surgery, Tokyo Dental College, Tokyo 101-0061, Japan.
Hideki MasakiCenter for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Hiromitsu NakauchiCenter for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305-5461, USA.
Takeshi NomuraDepartment of Oral Medicine, Oral and Maxillofacial Surgery, Tokyo Dental College, Chiba 272-8513, Japan.
Takahiko ShibaharaDepartment of Oral and Maxillofacial Surgery, Tokyo Dental College, Tokyo 101-0061, Japan.
Akira YamaguchiOral Health Science Center, Tokyo Dental College, Tokyo 101-0061, Japan.
Ung-Il ChungCenter for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8656, Japan; Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8655, Japan.
Toshifumi AzumaDepartment of Biochemistry, Tokyo Dental College, Tokyo 101-0061, Japan; Oral Health Science Center, Tokyo Dental College, Tokyo 101-0061, Japan. Electronic address: tazuma@tdc.ac.jp.
Shinsuke OhbaCenter for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8656, Japan; Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8655, Japan; Department of Cell Biology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521, Japan. Electronic address: s-ohba@nagasaki-u.ac.jp.
Tokyo Dental College · JPThe University of Tokyo · JPNagasaki University · JPStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two genetic diseases, Gorlin syndrome and McCune-Albright syndrome (MAS), show completely opposite symptoms in terms of bone mineral density and hedgehog (Hh) activity. In this study, we utilized human induced pluripotent stem cell (iPSC)-based models of the two diseases to understand the roles of Hh signaling in osteogenesis. Gorlin syndrome-derived iPSCs showed increased osteoblastogenesis and mineralization with Hh signaling activation and upregulation of a set of transcription factors in an osteogenic culture, compared with the isogenic control. MAS-specific iPSCs showed poor mineralization with low Hh signaling activity in the osteogenic culture; impaired osteoblastogenesis was restored to the normal level by treatment with an Hh signaling-activating small molecule. These data suggest that Hh signaling is a key controller for differentiation of osteoblasts from precursors. This study may pave a path to new drug therapies for genetic abnormalities in calcification caused by dysregulation of Hh signaling.

Indexed as

OsteogenesisBasal Cell Nevus SyndromeCell Culture TechniquesChromograninsGene Expression ProfilingGTP-Binding Protein alpha Subunits, GsHedgehog ProteinsHumansInduced Pluripotent Stem CellsMutationOsteoblastsSignal TransductionTranscription FactorsTranscriptomeChromograninsGNAS protein, humanGTP-Binding Protein alpha Subunits, GsHedgehog ProteinsTranscription Factorscalcificationfibrous dysplasiaGorlin syndromehedgehog pathwayMcCune-Albright syndromeosteogenesispatient-specific iPSC

Identifiers

PMID32531191
PMCPMC7363748
OpenAlexW3034910652

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.