Evidence map›Paper›PMID 37179642›Full record

ArticleACS omega2023

Quantitative Proteomics Reveals Transforming Growth Factor β Receptor Targeted by Resveratrol and Hesperetin Coformulation in Endothelial Cells.

Aktham Mestareehi, Hainan Li, Xiangmin Zhang, Sai Pranathi Meda Venkata, Ruchi Jaiswal, Fu-Shin Yu, Zhengping Yi, Jie-Mei Wang

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

8 authors at 1 institution in 1 country.

Aktham MestareehiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Hainan LiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Xiangmin ZhangDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Sai Pranathi Meda VenkataDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Ruchi JaiswalDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Fu-Shin YuDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Zhengping YiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.
Jie-Mei WangDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Integrated Biosciences, Ophthalmology, Visual and Anatomical Sciences, School of Medicine, and Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan 48201, United States.ORCID https://orcid.org/0000-0002-8723-4410
Eugene Applebaum College of Pharmacy and Health Sciences · US

Funding

Role of Inositol Requiring Enzyme 1 in Regulating Angiogenesis for Diabetic Wound RepairR01DK109036 · NIDDK · WAYNE STATE UNIVERSITY · PI WANG, JIEMEI · 2016 to 2020
$1.7M
Mechanistic study of Small-molecular Therapy in diabetic Wound HealingR01DK128937 · NIDDK · WAYNE STATE UNIVERSITY · PI WANG, JIEMEI, YI, ZHENGPING · 2021 to 2024
$1.6M
Alleviating Reactive Carbonyl Species-Induced Progenitor Cell Dysfunction in Diabetic Wound HealingR01DK119222 · NIDDK · WAYNE STATE UNIVERSITY · PI MONKS, TERRENCE J., WANG, JIEMEI · 2019 to 2022
$1.5M
NIDDK NIH HHS R01 DK109036NIDDK NIH HHS R01 DK119222NIDDK NIH HHS R01 DK128937
6 · The paper itself

Abstract

The endothelium is the frontline target of multiple metabolic stressors and pharmacological agents. As a consequence, endothelial cells (ECs) display highly dynamic and diverse proteome profiles. We describe here the culture of human aortic ECs from healthy and type 2 diabetic donors, the treatment with a small molecular coformulation of trans-resveratrol and hesperetin (tRES+HESP), followed by proteomic analysis of whole-cell lysate. A number of 3666 proteins were presented in all of the samples and thus further analyzed. We found that 179 proteins had a significant difference between diabetic ECs vs. healthy ECs, while 81 proteins had a significant change upon the treatment of tRES+HESP in diabetic ECs. Among them, 16 proteins showed a difference between diabetic ECs and healthy ECs and the difference was reversed by the tRES+HESP treatment. Follow-up functional assays identified activin A receptor-like type 1 and transforming growth factor β receptor 2 as the most pronounced targets suppressed by tRES+HESP in protecting angiogenesis

Identifiers

PMID37179642
PMCPMC10173440
OpenAlexW4366976850

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.