Evidence map›Paper›PMID 32266254›Full record

ArticleFrontiers in cell and developmental biology2020

Fibroblast Growth Factor 2 Attenuates Renal Ischemia-Reperfusion Injury via Inhibition of Endoplasmic Reticulum Stress.

Xiaohua Tan, Qianyu Tao, Guixiu Li, Lijun Xiang, Xiaomeng Zheng, Tianzhen Zhang, Cuijiao Wu, Dequan Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  7. Acute exposure to electronic cigarette components alters mRNA expression of pre-osteoblasts.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  8. Research Progress of Drug Delivery Systems Targeting the Kidneys.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
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  19. Article
  20. Antioxidants (Basel, Switzerland) · 2021
    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

8 authors at 4 institutions in 1 country.

Xiaohua TanDepartment of Pathology, School of Basic Medicine, Qingdao University, Qingdao, China.
Qianyu TaoSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Guixiu LiOutpatient Operating Room, Jiaozhou Central Hospital of Qingdao, Qingdao, China.
Lijun XiangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Xiaomeng ZhengSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Tianzhen ZhangDepartment of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao, China.
Cuijiao WuDepartment of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao, China.
Dequan LiDepartment of Traumatology Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Qingdao University · CNWenzhou Medical University · CNFirst Affiliated Hospital of Wenzhou Medical University · CNShuozhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute kidney injury (AKI) is a serious clinical disease that is mainly caused by renal ischemia-reperfusion (I/R) injury, sepsis, and nephrotoxic drugs. The pathologic mechanism of AKI is very complex and may involve oxidative stress, inflammatory response, autophagy, apoptosis, and endoplasmic reticulum (ER) stress. The basic fibroblast growth factor (FGF2) is a canonic member of the FGF family that plays a crucial role in various cellular processes, including organ development, wound healing, and tissue regeneration. However, few studies have reported the potential therapeutic effect of FGF2 in the repair of renal ischemic injury in the past two decades. In the present study, we investigated the protective effect of FGF2 on renal I/R injury using Sprague-Dawley and NRK-52E cells. Our results showed that FGF2 significantly attenuates the apoptosis of kidney tissues after I/R injury through the inhibition of excessive ER stress. Moreover, FGF2 also alleviated the excessive ER stress and apoptosis in cultured NRK-52E cells injured by tert-Butyl hydroperoxide (TBHP). Significantly, phosphatidylinositol 3-kinase (PI3K)-selective inhibitor LY294002 and mitogen-activated protein kinase kinase (MEK)-selective inhibitor U0126 were utilized in the present study to examine the protective mechanism of FGF2. Our

Indexed as

acute kidney injuryapoptosisER stressFGF2ischemia-reperfusion

Identifiers

PMID32266254
PMCPMC7105877
OpenAlexW3013929229

What OpenQuestion holds

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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.