Evidence map›Paper›PMID 38689508›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Polyacrylic Acid-Coated Selenium-Doped Carbon Dots Inhibit Ferroptosis to Alleviate Chemotherapy-Associated Acute Kidney Injury.

Jiahuan Li, Chengcheng Fu, Baoli Feng, Qingquan Liu, Jiangjiang Gu, Mohammad Nauman Khan, Lvhui Sun, Honghong Wu, Hao Wu

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–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

18 citing papers in PubMed.

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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.

Jiahuan LiState Key Laboratory of Agricultural Microbiology, College of Animal Science & Technology and College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China.ORCID 0000-0003-2395-5806
Chengcheng FuHubei Hongshan Laboratory, Wuhan, 430070, China.
Baoli FengState Key Laboratory of Agricultural Microbiology, College of Animal Science & Technology and College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China.
Qingquan LiuDepartment of Nephrology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Jiangjiang GuCollege of Chemistry, Huazhong Agricultural University, Wuhan, 430070, China.
Mohammad Nauman KhanSchool of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), Hainan University, Sanya, 572000, China.
Lvhui SunState Key Laboratory of Agricultural Microbiology, College of Animal Science & Technology and College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China.
Honghong WuHubei Hongshan Laboratory, Wuhan, 430070, China.
Hao WuState Key Laboratory of Agricultural Microbiology, College of Animal Science & Technology and College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, China.ORCID 0000-0001-5091-4562

Funding

Fundamental Research Funds for the Central Universities 2662023ZKPY002Hubei Agricultural Science and Technology Innovation Center Program 2021-620-000-001-032HZAU-AGIS Cooperation Fund SZYJY2021008National Key Research and Development Program of China 2022YFD2300205National Natural Science Foundation of China 32070738National Natural Science Foundation of China 32071971National Natural Science Foundation of China 32370808
6 · The paper itself

Abstract

Cisplatin-associated acute kidney injury (AKI) is a severe clinical syndrome that significantly restricts the chemotherapeutic application of cisplatin in cancer patients. Ferroptosis, a newly characterized programmed cell death driven by the lethal accumulation of lipid peroxidation, is widely reported to be involved in the pathogenesis of cisplatin-associated AKI. Targeted inhibition of ferroptosis holds great promise for developing novel therapeutics to alleviate AKI. Unfortunately, current ferroptosis inhibitors possess low bioavailability or perform non-specific accumulation in the body, making them inefficient in alleviating cisplatin-associated AKI or inadvertently reducing the anti-tumor efficacy of cisplatin, thus not suitable for clinical application. In this study, a novel selenium nanomaterial, polyacrylic acid-coated selenium-doped carbon dots (SeCD), is rationally developed. SeCD exhibits high biocompatibility and specifically accumulates in the kidney. Administration of SeCD effectively scavenges broad-spectrum reactive oxygen species and significantly facilitates GPX4 expression by releasing selenium, resulting in strong mitigation of ferroptosis in renal tubular epithelial cells and substantial alleviation of cisplatin-associated AKI, without compromising the chemotherapeutic efficacy of cisplatin. This study highlights a novel and promising therapeutic approach for the clinical prevention of AKI in cancer patients undergoing cisplatin chemotherapy.

Indexed as

Acrylic ResinsAcute Kidney InjuryCarbonCisplatinFerroptosisSeleniumAnimalsAntineoplastic AgentsDisease Models, AnimalHumansMaleMiceQuantum DotsAcrylic ResinsAntineoplastic AgentsCarboncarbopol 940CisplatinSeleniumacute kidney injurycarbon dotscisplatinferroptosisselenium

Identifiers

PMID38689508
PMCPMC11267338

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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.