Evidence map›Paper›PMID 35457038›Full record

ArticleInternational journal of molecular sciences2022

MIF1 and MIF2 Myostatin Peptide Inhibitors as Potent Muscle Mass Regulators.

Eun Ju Lee, Sibhghatulla Shaikh, Mohammad Hassan Baig, So-Young Park, Jeong Ho Lim, Syed Sayeed Ahmad, Shahid Ali, Khurshid Ahmad, Inho Choi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Effect ofHeliyon · 2024
    Article
  7. Article
  8. Review
  9. Review
  10. Therapeutic Applications of Ginseng Natural Compounds for Health Management.International journal of molecular sciences · 2023
    Review
  11. Review
  12. Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models.International journal of molecular sciences · 2022
    Review
  13. Dipeptidyl peptidase-4 inhibitory potentials ofFrontiers in molecular biosciences · 2022
    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

9 authors at 2 institutions in 1 country.

Eun Ju LeeDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0003-2496-0463
Sibhghatulla ShaikhDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0002-7489-2393
Mohammad Hassan BaigDepartment of Family Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06273, Korea.ORCID 0000-0001-8227-4838
So-Young ParkDepartment of Physiology, College of Medicine, Yeungnam University, Daegu 42415, Korea.
Jeong Ho LimDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0002-0375-8170
Syed Sayeed AhmadDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0002-2829-2768
Shahid AliDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0002-4724-5086
Khurshid AhmadDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.ORCID 0000-0002-1095-8445
Inho ChoiDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea.
Yeungnam University · KRYonsei University · KR

Funding

National Research Foundation of Korea 2020R1A6A1A03044512National Research Foundation of Korea NRF-2019R1C1C1006542National Research Foundation of Korea NRF-2021R1A2C2004177
6 · The paper itself

Abstract

The use of peptides as drugs has progressed over time and continues to evolve as treatment paradigms change and new drugs are developed. Myostatin (MSTN) inhibition therapy has shown great promise for the treatment of muscle wasting diseases. Here, we report the MSTN-derived novel peptides MIF1 (10-mer) and MIF2 (10-mer) not only enhance myogenesis by inhibiting MSTN and inducing myogenic-related markers but also reduce adipogenic proliferation and differentiation by suppressing the expression of adipogenic markers. MIF1 and MIF2 were designed based on in silico interaction studies between MSTN and its receptor, activin type IIB receptor (ACVRIIB), and fibromodulin (FMOD). Of the different modifications of MIF1 and MIF2 examined,

Indexed as

Muscular DiseasesMyostatinAnimalsFibromodulinMiceMuscle DevelopmentMusclesMuscle, SkeletalMuscular AtrophyPeptidesFibromodulinFmod protein, mouseMyostatinPeptidesmuscle regenerationmyogenesismyostatinpeptidesskeletal muscle

Identifiers

PMID35457038
PMCPMC9031736
OpenAlexW4223555072

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.