Evidence map›Paper›PMID 35565830›Full record

ArticleNutrients2022

miR-222 Is Involved in the Amelioration Effect of Genistein on Dexamethasone-Induced Skeletal Muscle Atrophy.

Mailin Gan, Jianfeng Ma, Jingyun Chen, Lei Chen, Shunhua Zhang, Ye Zhao, Lili Niu, Xuewei Li, Li Zhu, Linyuan Shen

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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

10 authors at 1 institution in 1 country.

Mailin GanDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.ORCID 0000-0001-9900-3559
Jianfeng MaDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Jingyun ChenDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Lei ChenDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Shunhua ZhangDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Ye ZhaoDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Lili NiuDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Xuewei LiDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Li ZhuDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Linyuan ShenDepartment of Animal Science, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.
Sichuan Agricultural University · CN

Funding

National Key Research and Development Program of China No. 2021YFD1200801National Natural Science Foundation of China No.31902135, No.31972524Sichuan Sci & Tech Support Program No. 2021YFYZ0030
6 · The paper itself

Abstract

Skeletal muscle atrophy is a complex degenerative disease characterized by decreased skeletal muscle mass, skeletal muscle strength, and function. MicroRNAs (miRNAs) are a potential therapeutic target, and natural products that regulate miRNA expression may be a safe and effective treatment strategy for muscle atrophy. Previous studies have shown beneficial effects of genistein treatment on muscle mass and muscle atrophy, but the mechanism is not fully understood. Differential co-expression network analysis revealed that miR-222 was upregulated in multiple skeletal muscle atrophy models. Subsequent in vitro (C2C12 myoblasts) and in vivo (C57BL/6 mice) experiments showed that genistein could alleviate dexamethasone-induced muscle atrophy and downregulate the expression of miR-222 in muscle tissue and C2C12 myotubes. The dual-luciferase reporter assay system confirmed that

Indexed as

GenisteinMicroRNAsAnimalsCell LineDexamethasoneMiceMice, Inbred C57BLMuscle Fibers, SkeletalMuscle, SkeletalMuscular AtrophyDexamethasoneGenisteinMicroRNAsMIRN222 microRNA, mousegenisteinIGF1miR-222muscle atrophy

Identifiers

PMID35565830
PMCPMC9104324
OpenAlexW4225263171

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.