Evidence map›Paper›PMID 36359891›Full record

ArticleCells2022

Role of lncRNA Has2os in Skeletal Muscle Differentiation and Regeneration.

Wanxin Chen, Weicai Chen, Peng Liu, Shiyu Qian, Shuang Tao, Mengchun Huang, Wanyi Xu, Cuiping Li, Xiaoyan Chen, Huizhu Lin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Wanxin ChenBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Weicai ChenBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Peng LiuLaboratory Medicine, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Shiyu QianDepartment of Public Health and Preventive Medicine, School of Medicine, Jinan University, Guangzhou 510632, China.
Shuang TaoBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Mengchun HuangBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Wanyi XuBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Cuiping LiBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Xiaoyan ChenBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Huizhu LinBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Zhenshu QinDepartment of Trauma Orthopaedics, Chenzhou First People's Hospital Affiliated to South China University, Chenzhou 423000, China.
Jianxi LuBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Shujuan XieBiotherapy Center, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.ORCID 0000-0002-0867-7273
Sun Yat-sen University · CNChenzhou First People's Hospital · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) regulate a series of physiological processes and play an important role in development, metabolism and disease. Our previous studies showed that lncRNAs involved in skeletal muscle differentiation. Here, we demonstrated that lncRNA Has2os is highly expressed in skeletal muscle and significantly elevated during skeletal cell differentiation. The knockdown of Has2os inhibited myocyte fusion and impeded the expression of the myogenic factors MyHC and Mef2C. Mechanically, Has2os regulates skeletal muscle differentiation by inhibiting the JNK/MAPK signaling pathway. Furthermore, we also revealed that Has2os is involved in the early stage of regeneration after muscle injury, and the JNK/MAPK signaling pathway is activated at both protein and mRNA levels during early repair. Our results demonstrate the new function of lncRNA Has2os, which plays crucial roles during skeletal muscle differentiation and muscle regeneration, providing a basis for the therapy of lncRNA-related muscle diseases.

Indexed as

RNA, Long NoncodingCell DifferentiationMuscle DevelopmentMuscle, SkeletalMyoblastsRNA, Long NoncodingHas2osJNK/MAPKlncRNAregenerationskeletal muscle differentiation

Identifiers

PMID36359891
PMCPMC9655701
OpenAlexW4308454290

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.