Evidence map›Paper›PMID 35976267›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2022

High expression of P4HA3 in obesity: a potential therapeutic target for type 2 diabetes.

Langen Zhuang, Can Li, Xiaolei Hu, Qingqing Yang, Xiaoyan Pei, Guoxi Jin

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 1 institution in 1 country.

Langen ZhuangDepartment of Endocrinology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China.ORCID http://orcid.org/0000-0003-3700-2715
Can LiShangyi Health Check-up Centre, Zibo, Shandong, China.ORCID http://orcid.org/0000-0002-9749-5016
Xiaolei HuDepartment of Endocrinology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China.ORCID http://orcid.org/0000-0001-7536-603X
Qingqing YangDepartment of Endocrinology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China.ORCID http://orcid.org/0000-0001-6214-3750
Xiaoyan PeiDepartment of Endocrinology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China.ORCID http://orcid.org/0000-0001-5404-8614
Guoxi JinDepartment of Endocrinology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, China.ORCID http://orcid.org/0000-0001-5944-9142
First Affiliated Hospital of Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aims of the present study were to evaluate the expression of prolyl 4-hydroxylase subunit alpha 3 (P4HA3) in adipocytes and adipose tissue and to explore its effect on obesity and type 2 diabetes mellitus (T2DM). We initially demonstrated that P4HA3 was significantly upregulated in the subcutaneous adipose tissue of obesity and T2DM patients, and its functional roles in adipocyte differentiation and insulin resistance were investigated using in vitro and in vivo models. The knockdown of P4HA3 inhibited adipocyte differentiation and improved insulin resistance in 3T3-L1 cells. In C57BL/6J db/db mice fed with a high fat diet (HFD), silencing P4HA3 significantly decreased fasting blood glucose and triglycerides (TG) levels, with concomitant decrease of body weight and adipose tissue weight. Further analysis showed that P4HA3 knockdown was correlated with the augmented IRS-1/PI3K/Akt/FoxO1 signaling pathway in the adipose and hepatic tissues of obese mice, which could improve hepatic glucose homeostasis and steatosis of mice. Together, our study suggested that the dysregulation of P4HA3 may contribute to the development of obesity and T2DM.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceProcollagen-Proline DioxygenaseAnimalsDiet, High-FatMiceMice, Inbred C57BLObesityPhosphatidylinositol 3-KinasesP4ha3 protein, mousePhosphatidylinositol 3-KinasesProcollagen-Proline Dioxygenase

Identifiers

PMID35976267
PMCPMC9377532
OpenAlexW4291821130

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.