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Naslov:Control compounds for preclinical drug-induced liver injury assessment : consensus-driven systematic review by the ProEuroDILI network
Avtorji:ID Segovia-Zafra, Antonio (Avtor)
ID Villanueva-Paz, Marina (Avtor)
ID Serras, Ana Sofia (Avtor)
ID Matilla-Cabello, Gonzalo (Avtor)
ID Bodoque-Garcia, Ana (Avtor)
ID Di Zeo-Sánchez, Daniel E. (Avtor)
ID Niu, Hao (Avtor)
ID Alvarez-Alvarez, Ismael (Avtor)
ID Sanz-Villanueva, Laura (Avtor)
ID Godec, Sergej (Avtor)
ID Milisav, Irina (Avtor), et al.
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,10 MB)
MD5: 228A2B3E5D3779820A3CB64CD559572D
 
URL URL - Izvorni URL, za dostop obiščite https://www.journal-of-hepatology.eu/article/S0168-8278(24)00325-8/fulltext
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Background & aims: Idiosyncratic drug-induced liver injury (DILI) is a complex and unpredictable event caused by drugs, and herbal or dietary supplements. Early identification of human hepatotoxicity at preclinical stages remains a major challenge, in which the selection of validated in vitro systems and test drugs has a significant impact. In this systematic review, we analyzed the compounds used in hepatotoxicity assays and established a list of DILI-positive and -negative control drugs for validation of in vitro models of DILI, supported by literature and clinical evidence and endorsed by an expert committee from the COST Action ProEuroDILI Network (CA17112). Methods: Following 2020 PRISMA guidelines, original research articles focusing on DILI which used in vitro human models and performed at least one hepatotoxicity assay with positive and negative control compounds, were included. Bias of the studies was assessed by a modified 'Toxicological Data Reliability Assessment Tool'. Results: A total of 51 studies (out of 2,936) met the inclusion criteria, with 30 categorized as reliable without restrictions. Although there was a broad consensus on positive compounds, the selection of negative compounds lacked clarity. 2D monoculture, short exposure times and cytotoxicity endpoints were the most tested, although there was no consensus on drug concentrations. Conclusions: Extensive analysis highlighted the lack of agreement on control compounds for in vitro DILI assessment. Following comprehensive in vitro and clinical data analysis together with input from the expert committee, an evidence-based consensus-driven list of 10 positive and negative control drugs for validation of in vitro models of DILI is proposed. Impact and implications: Prediction of human toxicity early in the drug development process remains a major challenge, necessitating the development of more physiologically relevant liver models and careful selection of drug-induced liver injury (DILI)-positive and -negative control drugs to better predict the risk of DILI associated with new drug candidates. Thus, this systematic study has crucial implications for standardizing the validation of new in vitro models of DILI. By establishing a consensus-driven list of positive and negative control drugs, the study provides a scientifically justified framework for enhancing the consistency of preclinical testing, thereby addressing a significant challenge in early hepatotoxicity identification. Practically, these findings can guide researchers in evaluating safety profiles of new drugs, refining in vitro models, and informing regulatory agencies on potential improvements to regulatory guidelines, ensuring a more systematic and efficient approach to drug safety assessment.
Ključne besede:clinical data, control compounds, drug-induced liver injury, expert committee, panel of control drugs, preclinical drug safety testing, validation of in vitro DILI models
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:str. 630-640
Številčenje:Vol. 81, iss. 4
PID:20.500.12556/DiRROS-30025 Novo okno
UDK:615.2:615.9
ISSN pri članku:0168-8278
DOI:10.1016/j.jhep.2024.04.026 Novo okno
COBISS.SI-ID:197028867 Novo okno
Opomba:
Datum objave v DiRROS:11.06.2026
Število ogledov:113
Število prenosov:96
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Journal of hepatology
Skrajšan naslov:J. hepatol.
Založnik:Elsevier
ISSN:0168-8278
COBISS.SI-ID:62487 Novo okno

Gradivo je financirano iz projekta

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Instituto de Salud Carlos III
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Številka projekta:PI21/01248
Naslov:FONDO EUROPEO DE DESARROLLO REGIONAL
Akronim:FEDER

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:PI19-00883
Naslov:Fondo Europeo de Desarrollo Regiona
Akronim:FEDER

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Številka projekta:PT23/00137
Naslov:FONDO EUROPEO DE DESARROLLO REGIONA
Akronim:FEDER

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:PEMP-0127-2020
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Akronim:FEDER

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:PI-0310-2018
Naslov:FONDO EUROPEO DE DESARROLLO REGIONAL
Akronim:FEDER

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Številka projekta:ISCIII
Naslov:iPFIS predoctoral contract
Akronim:IFI21/0034

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Spanish Ministry of Science, Innovation and Universities
Številka projekta:FPU22/03868
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Akronim:/

Financer:FCT - Fundação para a Ciência e a Tecnologia, I.P.
Številka projekta:2021.04902.BD
Naslov:Understanding the Underlying Mechanisms by which Mesenchymal Stem Cells Promote Liver Regeneration: The Specific Role of Exosomes EXO-THER

Financer:Drugi - Drug financer ali več financerjev
Program financ.:European Cooperation in Science and Technology
Številka projekta:CA17112
Naslov:/

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:PID2019-111669RB-100
Naslov:Plan Nacional de I+D

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Številka projekta:PID2022-1429560B-I00
Naslov:Plan Nacional de I+D

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Spanish Ministry of Science, Innovation and Universities
Številka projekta:PID2023AEP068
Naslov:Plan Nacional de I+D

Financer:EC - European Commission
Številka projekta:101095679
Naslov:Discovering chronic inflammation biomarkers that define key stages in the Healthy-to-NASH (non-alcoholic steatohepatitis) transition to inform early prevention and treatment strategies
Akronim:halt-RONIN

Financer:UKRI - UK Research and Innovation
Številka projekta:10067052
Naslov:halt-RONIN: Discovering chronic inflammation biomarkers that define key stages in the Healthy-to-NASH (non-alcoholic steatohepatitis) transition to inform early prevention and treatment strategies

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Generalitat de Catalunya
Številka projekta:SGR-2021-0049
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Akronim:AGAUR

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Fundació Marató TV3
Številka projekta:201916/31
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Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
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Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:klinični podatki, kontrolne spojine, z zdravili povzročena poškodba jeter, strokovna komisija, panel nadzornih zdravil, predklinično testiranje varnosti zdravil, validacija in vitro modelov DILI


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