Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues
Abstract Cell viability assays are an integral component of toxicology and high-throughput drug screening studies; however, many assays rely on a single biomarker of cell death which provides an incomplete assessment of cell viability. Here, we introduce an innovative approach that combines data fro...
Saved in:
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2025-01-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-025-86792-4 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832585846439542784 |
---|---|
author | Ahbid Zein-Sabatto Katerina St. Angelo Samantha J. Madnick Diane Hoffman-Kim Jeffrey R. Morgan Jonghwan Lee |
author_facet | Ahbid Zein-Sabatto Katerina St. Angelo Samantha J. Madnick Diane Hoffman-Kim Jeffrey R. Morgan Jonghwan Lee |
author_sort | Ahbid Zein-Sabatto |
collection | DOAJ |
description | Abstract Cell viability assays are an integral component of toxicology and high-throughput drug screening studies; however, many assays rely on a single biomarker of cell death which provides an incomplete assessment of cell viability. Here, we introduce an innovative approach that combines data from multiple assays using a linear mixed effects regression model and principal component analysis. We explored the cytotoxic response of various assay-treatment combinations using four assays with distinct mechanisms of action and seven different treatments across three types of microtissue cultures. The multi-assay data revealed the presence of multifaceted cellular injuries which highlight the need for multimodal approaches to better understand complex disruptions to viability. By incorporating outputs from the four assays, we introduced a new lethal concentration threshold that captures changes from different cellular injuries to provide a more comprehensive evaluation of cytotoxicity. Overall, the proposed approach provides a unique opportunity to analyze data from multiple assays in a holistic manner to improve the predictive power of drug screening and toxicology studies. |
format | Article |
id | doaj-art-67e76208ab8649f3b83f2c1845d285a6 |
institution | Kabale University |
issn | 2045-2322 |
language | English |
publishDate | 2025-01-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Scientific Reports |
spelling | doaj-art-67e76208ab8649f3b83f2c1845d285a62025-01-26T12:25:47ZengNature PortfolioScientific Reports2045-23222025-01-0115111610.1038/s41598-025-86792-4Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissuesAhbid Zein-Sabatto0Katerina St. Angelo1Samantha J. Madnick2Diane Hoffman-Kim3Jeffrey R. Morgan4Jonghwan Lee5School of Engineering, Brown UniversityDepartment of Pathology and Laboratory Medicine, Brown UniversityDepartment of Pathology and Laboratory Medicine, Brown UniversityInstitute for Biology, Engineering, and Medicine, Brown UniversitySchool of Engineering, Brown UniversitySchool of Engineering, Brown UniversityAbstract Cell viability assays are an integral component of toxicology and high-throughput drug screening studies; however, many assays rely on a single biomarker of cell death which provides an incomplete assessment of cell viability. Here, we introduce an innovative approach that combines data from multiple assays using a linear mixed effects regression model and principal component analysis. We explored the cytotoxic response of various assay-treatment combinations using four assays with distinct mechanisms of action and seven different treatments across three types of microtissue cultures. The multi-assay data revealed the presence of multifaceted cellular injuries which highlight the need for multimodal approaches to better understand complex disruptions to viability. By incorporating outputs from the four assays, we introduced a new lethal concentration threshold that captures changes from different cellular injuries to provide a more comprehensive evaluation of cytotoxicity. Overall, the proposed approach provides a unique opportunity to analyze data from multiple assays in a holistic manner to improve the predictive power of drug screening and toxicology studies.https://doi.org/10.1038/s41598-025-86792-4 |
spellingShingle | Ahbid Zein-Sabatto Katerina St. Angelo Samantha J. Madnick Diane Hoffman-Kim Jeffrey R. Morgan Jonghwan Lee Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues Scientific Reports |
title | Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues |
title_full | Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues |
title_fullStr | Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues |
title_full_unstemmed | Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues |
title_short | Multi-assay assessment of cytotoxicity reveals multiple mechanisms of action in 3D microtissues |
title_sort | multi assay assessment of cytotoxicity reveals multiple mechanisms of action in 3d microtissues |
url | https://doi.org/10.1038/s41598-025-86792-4 |
work_keys_str_mv | AT ahbidzeinsabatto multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues AT katerinastangelo multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues AT samanthajmadnick multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues AT dianehoffmankim multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues AT jeffreyrmorgan multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues AT jonghwanlee multiassayassessmentofcytotoxicityrevealsmultiplemechanismsofactionin3dmicrotissues |