Evidence map›Paper›PMID 37374154›Full record

ArticleLife (Basel, Switzerland)2023

Methyl Syringate Stimulates Glucose Uptake by Inhibiting Protein Tyrosine Phosphatases Relevant to Insulin Resistance.

Dohee Ahn, Jihee Kwon, Songyi Song, Jooyoung Lee, Sunyoung Yoon, Sang J Chung

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Exploring FourMolecules (Basel, Switzerland) · 2024
    Review
  5. Review
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

6 authors at 2 institutions in 1 country.

Dohee AhnSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0001-6661-5129
Jihee KwonDepartment of Biopharmaceutical Convergence, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Songyi SongDepartment of Biopharmaceutical Convergence, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Jooyoung LeeDepartment of Biopharmaceutical Convergence, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0009-0002-8415-9037
Sunyoung YoonDepartment of Cosmetic Science, Kwangju Women's University, Gwangju 62396, Republic of Korea.ORCID 0000-0002-5656-445X
Sang J ChungSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0002-3501-212X
Sungkyunkwan University · KRKwangju Women's University · KR

Funding

Bio & Medical Technology Development Program of the National Research Foundation (NRF) and funded by the Korean government (MSIT) NRF-2012M3A9C4048775Bio & Medical Technology Development Program of the National Research Foundation (NRF) and funded by the Korean government (MSIT) NRF-2022M3A9G8017838Bio & Medical Technology Development Program of the National Research Foundation (NRF) and funded by the Korean government (MSIT) NRF-2022M3A9G8084563
6 · The paper itself

Abstract

Several protein tyrosine phosphatases (PTPs), particularly PTPN1, PTPN2, PTPN6, PTPN9, PTPN11, PTPRS, and DUSP9, are involved in insulin resistance. Therefore, these PTPs could be promising targets for the treatment of type 2 diabetes. Our previous studies revealed that PTPN2 and PTPN6 are potential antidiabetic targets. Therefore, the identification of dual-targeting inhibitors of PTPN2 and PTPN6 could be a potential therapeutic strategy for the treatment or prevention of type 2 diabetes. In this study, we demonstrate that methyl syringate inhibits the catalytic activity of PTPN2 and PTPN6 in vitro, indicating that methyl syringate acts as a dual-targeting inhibitor of PTPN2 and PTPN6. Furthermore, methyl syringate treatment significantly increased glucose uptake in mature 3T3-L1 adipocytes. Additionally, methyl syringate markedly enhanced phosphorylation of adenosine monophosphate-activated protein kinase (AMPK) in 3T3L1 adipocytes. Taken together, our results suggest that methyl syringate, a dual-targeting inhibitor of PTPN2 and PTPN6, is a promising therapeutic candidate for the treatment or prevention of type 2 diabetes.

Indexed as

catalytic activityglucose uptakemethyl syringateprotein tyrosine phosphatases (PTPs)PTPN2PTPN6type 2 diabetes

Identifiers

PMID37374154
PMCPMC10302301
OpenAlexW4380631479

What Socratic 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 Socratic graph.