Evidence map›Paper›PMID 41089172›Full record

ArticleInternational journal of genomics2025

Growth Hormone Alleviates Atherosclerosis Through Regulating the Activity of PI3K/AKT Pathway: Insights From Single-Cell Sequence and Mechanism Exploration.

Jin Cai, Shuang Shi, Yuhang Wang, Xiangdong Zhang, Xinghua Wei, Yanjing Wu, Yunlong Shi, Bin Li, Daorong Hou

Abstract read
In one paragraph

Article in International journal of genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Jin CaiDepartment of Pediatrics, Affiliated Hospital of Nantong University, Nantong, China, ahnmc.com.ORCID https://orcid.org/0000-0001-9366-0793
Shuang ShiDepartment of Pediatrics, Medical College of Nantong University, Nantong, China.ORCID https://orcid.org/0009-0007-4446-7402
Yuhang WangDepartment of Pediatrics, Medical College of Nantong University, Nantong, China.ORCID https://orcid.org/0009-0007-3483-1776
Xiangdong ZhangDepartment of Pediatrics, Affiliated Hospital of Nantong University, Nantong, China, ahnmc.com.
Xinghua WeiDepartment of Pediatrics, Medical College of Nantong University, Nantong, China.ORCID https://orcid.org/0009-0009-4043-8430
Yanjing WuDepartment of Pediatrics, Medical College of Nantong University, Nantong, China.ORCID https://orcid.org/0009-0008-4477-7379
Yunlong ShiDepartment of Pediatrics, Medical College of Nantong University, Nantong, China.ORCID https://orcid.org/0009-0003-9948-2344
Bin LiDepartment of Pediatrics, Affiliated Hospital of Nantong University, Nantong, China, ahnmc.com.ORCID https://orcid.org/0000-0002-0846-8797
Daorong HouKey Laboratory of Model Animal Research, Animal Core Facility, Nanjing Medical University, Nanjing, China, njmu.edu.cn.ORCID https://orcid.org/0000-0002-7755-9326

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This research sought to investigate the impact and underlying mechanisms of growth hormone (GH) on atherosclerosis (AS) based on the analysis of single-cell RNA sequencing (scRNA-seq) data. Methods: We analyzed the impact of GH on arterial vascular smooth muscle cells (VSMCs) by utilizing scRNA-seq data obtained from both atherosclerotic and healthy vascular tissues in mice. AS was induced in C57BL/6 and ApoE Results: scRNA-seq data analysis showed that growth hormone signaling was reduced in VSMCs of atherosclerotic arteries. HFD led to elevated levels of serum total cholesterol (TC), triglycerides (TGs), and low-density lipoprotein cholesterol (LDL-C), accompanied by increased lipid deposition, inflammatory responses, and oxidative stress. In contrast, high-density lipoprotein cholesterol (HDL-C) and insulin-like growth factor 1 (IGF-1) levels were lower in C57-Hx mice. GH treatment improved HFD-induced AS in ApoE Conclusion: GH alleviates the development of AS through the activation of the PI3K/AKT pathway. The findings of this research emphasize the therapeutic potential of GH in inhibiting AS and highlight the importance of the PI3K/AKT pathway as a promising target for clinical intervention.

Indexed as

atherosclerosisgrowth hormoneinflammatory responsesoxidative stressPI3K/AKT signaling pathway

Identifiers

PMID41089172
PMCPMC12516355

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.