Evidence map›Paper›PMID 29650965›Full record

ArticleNature communications2018

A novel autophagy enhancer as a therapeutic agent against metabolic syndrome and diabetes.

Hyejin Lim, Yu-Mi Lim, Kook Hwan Kim, Young Eui Jeon, Kihyoun Park, Jinyoung Kim, Hui-Yun Hwang, Dong Jin Lee, Haushabhau Pagire, Ho Jeong Kwon and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

90 citing papers in PubMed, 157 citations in OpenAlex.

  1. Review
  2. Lipophagy and lipid droplets in neurodegeneration.Trends in pharmacological sciences · 2026
    Review
  3. Trehalose's untapped mechanisms in alzheimer's: gut-brain-autophagy signalling beyond the usual targets.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Autophagy in Sensorineural Hearing Loss: Jekyll or Hyde?International journal of molecular sciences · 2026
    Review
  10. Article
  11. Autophagy activator AA-20 improves proteostasis and extendsProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Hyejin LimSeverance Biomedical Science Institute, Seoul, Korea.
Yu-Mi LimSeverance Biomedical Science Institute, Seoul, Korea.
Kook Hwan KimSeverance Biomedical Science Institute, Seoul, Korea.
Young Eui JeonDepartment of Oral Biology, Yonsei University College of Dentistry, Seoul, Korea.
Kihyoun ParkDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Jinyoung KimSeverance Biomedical Science Institute, Seoul, Korea.
Hui-Yun HwangGlobal Research Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.
Dong Jin LeeGlobal Research Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.
Haushabhau PagireDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, Korea.
Ho Jeong KwonGlobal Research Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.ORCID http://orcid.org/0000-0002-6919-833X
Jin Hee AhnDepartment of Chemistry, Gwangju Institute of Science and Technology, Gwangju, Korea.
Myung-Shik LeeSeverance Biomedical Science Institute, Seoul, Korea. mslee0923@yuhs.ac.ORCID http://orcid.org/0000-0003-3292-1720
Yonsei University · KRSeverance Hospital · KRGwangju Institute of Science and Technology · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a critical regulator of cellular homeostasis, dysregulation of which is associated with diverse diseases. Here we show therapeutic effects of a novel autophagy enhancer identified by high-throughput screening of a chemical library against metabolic syndrome. An autophagy enhancer increases LC3-I to LC3-II conversion without mTOR inhibition. MSL, an autophagy enhancer, activates calcineurin, and induces dephosphorylation/nuclear translocation of transcription factor EB (TFEB), a master regulator of lysosomal biogenesis and autophagy gene expression. MSL accelerates intracellular lipid clearance, which is reversed by lalistat 2 or Tfeb knockout. Its administration improves the metabolic profile of ob/ob mice and ameliorates inflammasome activation. A chemically modified MSL with increased microsomal stability improves the glucose profile not only of ob/ob mice but also of mice with diet-induced obesity. Our data indicate that our novel autophagy enhancer could be a new drug candidate for diabetes or metabolic syndrome with lipid overload.

Indexed as

AnimalsAutophagyDiabetes MellitusHeLa CellsHumansHypoglycemic AgentsLipid MetabolismMaleMetabolic SyndromeMetabolomeMiceMice, Inbred C57BLMice, KnockoutMice, ObeseObesityOxazoles4-(4-fluorophenyl)sulfonyl-5-methylthio-2-phenyloxazoleHypoglycemic AgentsOxazoles

Identifiers

PMID29650965
PMCPMC5897400
OpenAlexW2798211916

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.