Evidence map›Paper›PMID 37193023›Full record

ArticlePeerJ2023

Tandem mass tag-based quantitative proteomic analysis identification of succinylation related proteins in pathogenesis of thoracic aortic aneurysm and aortic dissection.

Yu Zhang, Hongwei Zhang, Haiyue Wang, Chenhao Wang, Peng Yang, Chen Lu, Yu Liu, Zhenyuan Xu, Yi Xie, Jia Hu

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Precision Profiling of the Cardiovascular Post-Translationally Modified Proteome.Journal of cardiovascular development and disease · 2026
    Review
  6. Review
  7. 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.

Yu Zhang *Department of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Hongwei Zhang *Department of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Haiyue WangDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Chenhao WangDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0002-3275-8241
Peng YangDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Chen LuDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Yu LiuDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Zhenyuan XuDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Yi XieDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Jia HuDepartment of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Thoracic aortic aneurysm and dissection (TAAD) are devastating cardiovascular diseases with a high rate of disability and mortality. Lysine succinylation, a newly found post-translational modification, has been reported to play an important role in cardiovascular diseases. However, how succinylation modification influences TAAD remains obscure. Methods: Ascending aortic tissues were obtained from patients with thoracic aortic aneurysm (TAA, Results: The level of global lysine succinylation significantly increased in TAA and TAD patients compared with healthy subjects. Of all proteins identified by proteomic analysis, 197 common DEPs were screened both in TAA and TAD group compared with the control group, of which 93 proteins were significantly upregulated while 104 were downregulated. Among these 197 DEPs, OXCT1 overlapped with the succinylation-related proteins and was selected as the target protein involved in thoracic aortic pathogenesis. OXCT1 was further verified by Western blotting and qRT-PCR, and the results showed that OXCT1 in TAA and TAD patients was significantly lower than that in healthy donors ( Conclusions: OXCT1 represents novel biomarkers for lysine succinylation of TAAD and might be a therapeutic target in the future.

Indexed as

Aortic AneurysmAortic Aneurysm, ThoracicAortic DissectionAzidesDeoxyglucoseHumansLysineProteomics1,3,4,6-tetra-O-acetyl-2-azido-2-deoxyglucopyranoseAzidesDeoxyglucoseLysineOXCT1ProteomicsSuccinylationTandem mass tag labellingThoracic aortic aneurysmThoracic aortic dissection

Identifiers

PMID37193023
PMCPMC10183161
OpenAlexW4376872149

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.