Evidence map›Paper›PMID 37686441›Full record

ArticleInternational journal of molecular sciences2023

A Novel Long Noncoding RNA in Osteocytes Regulates Bone Formation through the Wnt/β-Catenin Signaling Pathway.

Makoto Arai, Hiroki Ochi, Satoko Sunamura, Nobuaki Ito, Masaomi Nangaku, Shu Takeda, Shingo Sato

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Comparative Effects ofInternational journal of molecular sciences · 2026
    Article
  2. Review
  3. 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

7 authors at 4 institutions in 1 country.

Makoto AraiDivision of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo 113-8655, Japan.
Hiroki OchiDepartment of Rehabilitation for Motor Functions, Research Institute, National Rehabilitation Center for Persons with Disabilities, Tokorozawa 359-8555, Japan.
Satoko SunamuraDepartment of Orthopaedic Surgery, Graduate School, Tokyo Medical and Dental University (TMDU), Tokyo 113-8519, Japan.
Nobuaki ItoDivision of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo 113-8655, Japan.ORCID 0000-0002-4071-5372
Masaomi NangakuDivision of Nephrology and Endocrinology, The University of Tokyo Hospital, Tokyo 113-8655, Japan.
Shu TakedaDivision of Endocrinology, Toranomon Hospital Endocrine Center, Tokyo 105-8470, Japan.
Shingo SatoCenter for Innovative Cancer Treatment, Tokyo Medical and Dental University (TMDU), Tokyo 113-8519, Japan.ORCID 0000-0002-6227-5910
University of Tokyo Hospital · JPTokyo Medical and Dental University · JPNational Rehabilitation Center for Persons with Disabilities · JPToranomon Hospital · JP

Funding

Grants-in-Aid for Scientific Research (KAKENHI) #19H03777Grants-in-Aid for Scientific Research (KAKENHI) #19K22680Grants-in-Aid for Scientific Research (KAKENHI) #21K19556Grants-in-Aid for Scientific Research (KAKENHI) #22H03196the Core Research for Evolutional Science and Technology (CREST) #177ggm06100088h h0005
6 · The paper itself

Abstract

The vast majority of transcribed RNAs are noncoding RNAs. Among noncoding RNAs, long noncoding RNAs (lncRNAs), which contain hundreds to thousands of bases, have received attention in many fields. The vast majority of the constituent cells in bone tissue are osteocytes, but their regulatory mechanisms are incompletely understood. Considering the wide range of potential contributions of lncRNAs to physiological processes and pathological conditions, we hypothesized that lncRNAs in osteocytes, which have not been reported, could be involved in bone metabolism. Here, we first isolated osteocytes from femurs of mice with osteocyte-specific GFP expression. Then, through RNA-sequencing, we identified osteocyte-specific lncRNAs and focused on a novel lncRNA, 9530026P05Rik (lncRNA953Rik), which strongly suppressed osteogenic differentiation. In the IDG-SW3 osteocyte line with lncRNA953Rik overexpression, the expression of

Indexed as

OsteocytesOsteogenesisRNA, Long NoncodingAnimalsChromatography, LiquidMiceTandem Mass SpectrometryWnt Signaling PathwayRNA, Long Noncodingbone formationlong noncoding RNAosteocyte

Identifiers

PMID37686441
PMCPMC10488071
OpenAlexW4386409588

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.