Evidence map›Paper›PMID 35347248›Full record

ArticleActa pharmacologica Sinica2022

Dihydroartemisinin suppresses renal fibrosis in mice by inhibiting DNA-methyltransferase 1 and increasing Klotho.

Wei Zhou, Min-Min Chen, Hui-Ling Liu, Zi-Lin Si, Wen-Hui Wu, Hong Jiang, Lin-Xiao Wang, Nosratola D Vaziri, Xiao-Fei An, Ke Su and 3 more

Abstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–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

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Asiatic acid fromFrontiers in nutrition · 2026
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  11. [Potential of early diagnosis and targeted therapy for Klotho protein in chronic kidney disease].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 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

13 authors.

Wei Zhou *State Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Min-Min Chen *State Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Hui-Ling Liu *State Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Zi-Lin SiState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Wen-Hui WuState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Hong JiangState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Lin-Xiao WangState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Nosratola D VaziriDivision of Nephrology and Hypertension, School of Medicine, University of California Irvine, Irvine, CA, USA.
Xiao-Fei AnAffiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Ke SuDepartment of Nephrology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Cheng ChenDepartment of Nephrology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Ning-Hua TanState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. nhtan@cpu.edu.cn.
Zhi-Hao ZhangState Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. zzh-198518@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal fibrosis is an unavoidable end result of all forms of progressive chronic kidney diseases (CKD). Discovery of efficacious drugs against renal fibrosis is in crucial need. In a preliminary study we found that a derivative of artemisinin, dihydroartemisinin (DHA), exerted strong renoprotection, and reversed renal fibrosis in adenine-induced CKD mouse model. In this study we investigated the anti-fibrotic mechanisms of DHA, particularly its specific target in renal cells. Renal fibrosis was induced in mice by unilateral ureteral obstruction (UUO) or oral administration of adenine (80 mg · kg

Indexed as

ArtemisininsKidneyRenal Insufficiency, ChronicUreteral ObstructionAdenineAnimalsAzacitidinebeta CateninBiotinDNADNA Modification MethylasesFibrosisGlucuronidaseHEK293 CellsHumansKlotho ProteinsAdenineArtemisininsartenimolAzacitidinebeta CateninBiotinDNADNA Modification MethylasesGlucuronidaseKlotho ProteinsProteasome Endopeptidase ComplexTransforming Growth Factor betaTransforming Growth Factor beta1Ubiquitins5-azacytidineaffinity-based proteome profilingdihydroartemisininDNMT1Klothorenal fibrosis

Identifiers

PMID35347248
PMCPMC9525601

What OpenQuestion holds

Textmetadata
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.