Evidence map›Paper›PMID 36883930›Full record

ReviewCell proliferation2023

Ubiquitin-specific peptidases: Players in bone metabolism.

Jianlin Shen, Xiaoning Lin, Feifei Dai, Guoli Chen, Haibin Lin, Bangjiang Fang, Huan Liu

Open access · goldAbstract readReview
In one paragraph

Review in Cell proliferation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  12. Deubiquitylating Enzymes in Hepatocellular Carcinoma.International journal of biological sciences · 2025
    Review
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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

7 authors at 2 institutions in 1 country.

Jianlin ShenDepartment of Orthopaedics, Affiliated Hospital of Putian University, Putian, China.ORCID https://orcid.org/0000-0002-1130-0653
Xiaoning LinDepartment of Orthopaedics, Affiliated Hospital of Putian University, Putian, China.
Feifei DaiSchool of Medicine, Putian Universtiy, Putian, China.
Guoli ChenDepartment of Orthopaedics, Affiliated Hospital of Putian University, Putian, China.
Haibin LinDepartment of Orthopaedics, Affiliated Hospital of Putian University, Putian, China.
Bangjiang FangDepartment of Emergency, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Huan LiuDepartment of Orthopaedics, Affiliated Hospital of Putian University, Putian, China.
Putian University · CNShanghai University of Traditional Chinese Medicine · CN

Funding

Natural Science Foundation of Fujian Province 2020J011260Putian Science and Technology Bureau 2060499Research Foundation Project of Putian University 2019070
6 · The paper itself

Abstract

Osteoporosis is an ageing-related disease, that has become a major public health problem and its pathogenesis has not yet been fully elucidated. Substantial evidence suggests a strong link between overall age-related disease progression and epigenetic modifications throughout the life cycle. As an important epigenetic modification, ubiquitination is extensively involved in various physiological processes, and its role in bone metabolism has attracted increasing attention. Ubiquitination can be reversed by deubiquitinases, which counteract protein ubiquitination degradation. As the largest and most structurally diverse cysteinase family of deubiquitinating enzymes, ubiquitin-specific proteases (USPs), comprising the largest and most structurally diverse cysteine kinase family of deubiquitinating enzymes, have been found to be important players in maintaining the balance between bone formation and resorption. The aim of this review is to explore recent findings highlighting the regulatory functions of USPs in bone metabolism and provide insight into the molecular mechanisms governing their actions during bone loss. An in-deep understanding of USPs-mediated regulation of bone formation and bone resorption will provide a scientific rationale for the discovery and development of novel USP-targeted therapeutic strategies for osteoporosis.

Indexed as

Ubiquitin-Specific ProteasesUbiquitinationUbiquitin-Specific Proteases

Identifiers

PMID36883930
PMCPMC10392067
OpenAlexW4323534601

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.