Evidence map›Paper›PMID 36852327›Full record

ArticleOxidative medicine and cellular longevity2023

Anlotinib Alleviates Renal Fibrosis via Inhibition of the ERK and AKT Signaling Pathways.

Donglin Sun, Jing Guo, Weifei Liang, Yangxiao Chen, Xiangqiu Chen, Li Wang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-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

9 citing papers in PubMed, 6 citations in OpenAlex.

  1. S100A4 Orchestrates Fibroblast Fate to Drive Fibrotic Remodeling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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 4 institutions in 1 country.

Donglin SunGuangzhou Medical University, Guangzhou 510000, China.ORCID https://orcid.org/0000-0003-2963-6021
Jing GuoGuangzhou Medical University, Guangzhou 510000, China.ORCID https://orcid.org/0000-0002-6434-2021
Weifei LiangQingyuan People's Hospital, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan 511500, China.ORCID https://orcid.org/0000-0003-3999-5925
Yangxiao ChenGuangzhou Medical University, Guangzhou 510000, China.ORCID https://orcid.org/0000-0002-1015-0649
Xiangqiu ChenDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen 518100, China.ORCID https://orcid.org/0000-0001-8432-5299
Li WangSouthern Medical University Affiliated Longhua People's Hospital, Nephrology Department, Shenzhen, 518020 Guangdong, China.ORCID https://orcid.org/0000-0001-8166-9408
Guangzhou Medical University · CNSouthern Medical University · CNSouthern Medical University Shenzhen Hospital · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We examined whether anlotinib can attenuate folic acid-induced and unilateral ureteral obstruction-induced renal fibrosis and explored the underlying antifibrotic mechanism. Materials and Methods: We have evaluated the effects of anlotinib on folic acid-induced and unilateral ureteral obstruction-induced renal fibrosis in mice through in vivo experiments of unilateral ureteral obstruction or folic acid-induced interstitial fibrosis and in vitro models of transforming growth factor- Results: Anlotinib improved proteinuria and reduced renal impairment in folic acid-induced mouse models of renal fibrosis. Anlotinib reduced tubular injury, deposition of tubular extracellular matrix, and expression of alpha-smooth muscle actin, transforming growth factor- Conclusions: Anlotinib ameliorated renal function, improved extracellular matrix deposition, reduced protein levels of epithelial-mesenchymal transition markers, and decreased cellular inflammatory factors. Anlotinib reduced renal injury and fibrosis by inhibiting the transforming growth factor-

Indexed as

Kidney DiseasesUreteral ObstructionAnimalsFibrosisFolic AcidHumansIndolesMiceProto-Oncogene Proteins c-aktQuinolinesSignal TransductionTransforming Growth Factor beta1anlotinibFolic AcidIndolesProto-Oncogene Proteins c-aktQuinolinesTransforming Growth Factor beta1

Identifiers

PMID36852327
PMCPMC9966823
OpenAlexW4321328480

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.