Use of in vitro 3D tissue models in genotoxicity testing: Strategic fit, validation status and way forward. Report of the working group from the 7th International Workshop on Genotoxicity Testing (IWGT)
•Extensive progress made in development of 3D organ-based genotoxicity assays.•3D culture models represent major exposure routes: dermal, oral, inhalation.•The 3D skin comet and MN assays are considered mature and sufficiently validated.•Liver and airway model-based genotoxicity assays show promise...
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| Published in | Mutation Research/Genetic Toxicology and Environmental Mutagenesis Vol. 850-851; p. 503135 |
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| Main Authors | , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English Japanese |
| Published |
Elsevier B.V
01.02.2020
Elsevier BV |
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| Online Access | Get full text |
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| Abstract | •Extensive progress made in development of 3D organ-based genotoxicity assays.•3D culture models represent major exposure routes: dermal, oral, inhalation.•The 3D skin comet and MN assays are considered mature and sufficiently validated.•Liver and airway model-based genotoxicity assays show promise but are at early stage.
Use of three-dimensional (3D) tissue equivalents in toxicology has been increasing over the last decade as novel preclinical test systems and as alternatives to animal testing. In the area of genetic toxicology, progress has been made with establishing robust protocols for skin, airway (lung) and liver tissue equivalents. In light of these advancements, a “Use of 3D Tissues in Genotoxicity Testing” working group (WG) met at the 7th IWGT meeting in Tokyo in November 2017 to discuss progress with these models and how they may fit into a genotoxicity testing strategy. The workshop demonstrated that skin models have reached an advanced state of validation following over 10 years of development, while liver and airway model-based genotoxicity assays show promise but are at an early stage of development. Further effort in liver and airway model-based assays is needed to address the lack of coverage of the three main endpoints of genotoxicity (mutagenicity, clastogenicity and aneugenicity), and information on metabolic competence. The IWGT WG believes that the 3D skin comet and micronucleus assays are now sufficiently validated to undergo an independent peer review of the validation study, followed by development of individual OECD Test Guidelines. |
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| AbstractList | •Extensive progress made in development of 3D organ-based genotoxicity assays.•3D culture models represent major exposure routes: dermal, oral, inhalation.•The 3D skin comet and MN assays are considered mature and sufficiently validated.•Liver and airway model-based genotoxicity assays show promise but are at early stage.
Use of three-dimensional (3D) tissue equivalents in toxicology has been increasing over the last decade as novel preclinical test systems and as alternatives to animal testing. In the area of genetic toxicology, progress has been made with establishing robust protocols for skin, airway (lung) and liver tissue equivalents. In light of these advancements, a “Use of 3D Tissues in Genotoxicity Testing” working group (WG) met at the 7th IWGT meeting in Tokyo in November 2017 to discuss progress with these models and how they may fit into a genotoxicity testing strategy. The workshop demonstrated that skin models have reached an advanced state of validation following over 10 years of development, while liver and airway model-based genotoxicity assays show promise but are at an early stage of development. Further effort in liver and airway model-based assays is needed to address the lack of coverage of the three main endpoints of genotoxicity (mutagenicity, clastogenicity and aneugenicity), and information on metabolic competence. The IWGT WG believes that the 3D skin comet and micronucleus assays are now sufficiently validated to undergo an independent peer review of the validation study, followed by development of individual OECD Test Guidelines. Use of three-dimensional (3D) tissue equivalents in toxicology has been increasing over the last decade as novel preclinical test systems and as alternatives to animal testing. In the area of genetic toxicology, progress has been made with establishing robust protocols for skin, airway (lung) and liver tissue equivalents. In light of these advancements, a "Use of 3D Tissues in Genotoxicity Testing" working group (WG) met at the 7th IWGT meeting in Tokyo in November 2017 to discuss progress with these models and how they may fit into a genotoxicity testing strategy. The workshop demonstrated that skin models have reached an advanced state of validation following over 10 years of development, while liver and airway model-based genotoxicity assays show promise but are at an early stage of development. Further effort in liver and airway model-based assays is needed to address the lack of coverage of the three main endpoints of genotoxicity (mutagenicity, clastogenicity and aneugenicity), and information on metabolic competence. The IWGT WG believes that the 3D skin comet and micronucleus assays are now sufficiently validated to undergo an independent peer review of the validation study, followed by development of individual OECD Test Guidelines.Use of three-dimensional (3D) tissue equivalents in toxicology has been increasing over the last decade as novel preclinical test systems and as alternatives to animal testing. In the area of genetic toxicology, progress has been made with establishing robust protocols for skin, airway (lung) and liver tissue equivalents. In light of these advancements, a "Use of 3D Tissues in Genotoxicity Testing" working group (WG) met at the 7th IWGT meeting in Tokyo in November 2017 to discuss progress with these models and how they may fit into a genotoxicity testing strategy. The workshop demonstrated that skin models have reached an advanced state of validation following over 10 years of development, while liver and airway model-based genotoxicity assays show promise but are at an early stage of development. Further effort in liver and airway model-based assays is needed to address the lack of coverage of the three main endpoints of genotoxicity (mutagenicity, clastogenicity and aneugenicity), and information on metabolic competence. The IWGT WG believes that the 3D skin comet and micronucleus assays are now sufficiently validated to undergo an independent peer review of the validation study, followed by development of individual OECD Test Guidelines. |
| ArticleNumber | 503135 |
| Author | Kirkland, David Corvi, Raffaella Dusinska, Maria Yang, Ying van Acker, Frédérique Pfuhler, Stefan van Benthem, Jan Heflich, Robert H. Curren, Rodger Kidd, Darren Ouedraogo, Gladys Hayashi, Makoto Doak, Shareen H. Reisinger, Kerstin Sofuni, Toshio Luan, Yang |
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| Keywords | Micronucleus test In vitro genotoxicity testing DNA damage Reconstructed human skin 3D airway models Comet assay Liver spheroids |
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| Snippet | •Extensive progress made in development of 3D organ-based genotoxicity assays.•3D culture models represent major exposure routes: dermal, oral, inhalation.•The... Use of three-dimensional (3D) tissue equivalents in toxicology has been increasing over the last decade as novel preclinical test systems and as alternatives... |
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| SubjectTerms | 3D airway models Comet assay DNA damage In vitro genotoxicity testing Liver spheroids Micronucleus test Reconstructed human skin |
| Title | Use of in vitro 3D tissue models in genotoxicity testing: Strategic fit, validation status and way forward. Report of the working group from the 7th International Workshop on Genotoxicity Testing (IWGT) |
| URI | https://dx.doi.org/10.1016/j.mrgentox.2020.503135 https://cir.nii.ac.jp/crid/1870020693131252992 https://www.proquest.com/docview/2386428563 |
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