Evidence map›Paper›PMID 31929748›Full record

ArticleInternational journal of biological sciences2020

Ruxolitinib Alleviates Renal Interstitial Fibrosis in UUO Mice.

Yu Bai, Wei Wang, Ping Yin, Jian Gao, Lei Na, Yu Sun, Zhuo Wang, Zhongbo Zhang, Chenghai Zhao

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

54 citing papers in PubMed, 103 citations in OpenAlex.

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  13. Antioxidants (Basel, Switzerland) · 2025
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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

9 authors at 1 institution in 1 country.

Yu BaiDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Wei WangDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Ping YinDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Jian GaoCenter of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, China.
Lei NaDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Yu SunDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Zhuo WangDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Zhongbo ZhangDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Chenghai ZhaoDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ruxolitinib is a selective inhibitor of Jak1/2. Downstream signaling pathways of Jak, such as Stat3 and Akt/mTOR, are overactivated and contribute to renal interstitial fibrosis. Therefore, we explored the effect of Ruxolitinib on this pathological process. Unilateral ureteral obstruction (UUO) models and TGF-β1-treated fibroblasts and renal tubular epithelial cells were adopted in this study. Ruxolitinib was administered to UUO mice and TGF-β1-treated cells. Kidneys from UUO mice with Ruxolitinib treatment displayed less tubular injuries compared with those without Ruxolitinib treatment. Ruxolitinib treatment suppressed fibroblast activation and extracellular matrix (ECM) production in UUO kidneys and TGF-β1-treated fibroblasts. Ruxolitinib treatment also blocked epithelial-mesenchymal transition (EMT) in UUO kidneys and TGF-β 1-treated renal tubular epithelial cells. Moreover, Ruxolitinib treatment alleviated UUO-induced inflammation, oxidative stress and apoptosis. Mechanistically, Ruxolitinib treatment attenuated activation of both Stat3 and Akt/mTOR/Yap pathways. In conclusion, Ruxolitinib treatment can ameliorate UUO-induced renal interstitial fibrosis, suggesting that Ruxolitinib may be potentially used to treat fibrotic kidney disease.

Indexed as

AnimalsApoptosisBlotting, WesternCell LineChemokine CCL2Epithelial CellsEpithelial-Mesenchymal TransitionFibroblastsFibrosisImmunohistochemistryIn Situ Nick-End LabelingJanus Kinase 1Janus Kinase 2Kidney DiseasesMaleMiceChemokine CCL2Janus Kinase 1Janus Kinase 2NitrilesPyrazolesPyrimidinesRNA, MessengerruxolitinibSTAT3 Transcription FactorTransforming Growth Factor beta1JakmTORRuxolitinibStat3TGF-β1

Identifiers

PMID31929748
PMCPMC6949153
OpenAlexW2992524785

What OpenQuestion holds

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Registered trials

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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.